Trial Outcomes & Findings for PF-00299804 As A Single Agent, In Patients With Advanced Non-Small Cell Lung Cancer Who Have Failed Chemotherapy And Erlotinib (NCT NCT00548093)
NCT ID: NCT00548093
Last Updated: 2019-05-21
Results Overview
BOR:best response recorded from treatment start until disease progression as per Response Evaluation Criteria in Solid Tumors (RECIST). Complete Response: disappearance of all lesions. Partial Response (PR):greater than or equal to (\>=)30% decrease in sum of longest diameters (SLDs) of target lesions (TLs) taking as reference baseline SLD. Progressive disease (PD):\>=20% increase in SLD of TLs taking as reference smallest SLD since treatment start, or appearance of \>=1 new lesion. Stable disease:neither shrinkage for PR nor increase for PD taking as reference smallest SLD since treatment start.
COMPLETED
PHASE2
66 participants
Baseline, end of every even-numbered cycle up to end of treatment (Day 936)
2019-05-21
Participant Flow
Participant milestones
| Measure |
PF-00299804 (Adenocarcinoma Histology)
Participants with adenocarcinoma histology received PF-00299804 tablet 45 milligram (mg) orally once daily in cycles of 21 days until unacceptable toxicity, tumor progression, death, withdrawal from the study or investigator's discretion.
|
PF-00299804 (Non-adenocarcinoma Histology)
Participants with non-adenocarcinoma histology received PF-00299804 tablet 45 mg orally once daily in cycles of 21 days until unacceptable toxicity, tumor progression, death, withdrawal from the study or investigator's discretion.
|
|---|---|---|
|
Overall Study
STARTED
|
50
|
16
|
|
Overall Study
COMPLETED
|
0
|
0
|
|
Overall Study
NOT COMPLETED
|
50
|
16
|
Reasons for withdrawal
| Measure |
PF-00299804 (Adenocarcinoma Histology)
Participants with adenocarcinoma histology received PF-00299804 tablet 45 milligram (mg) orally once daily in cycles of 21 days until unacceptable toxicity, tumor progression, death, withdrawal from the study or investigator's discretion.
|
PF-00299804 (Non-adenocarcinoma Histology)
Participants with non-adenocarcinoma histology received PF-00299804 tablet 45 mg orally once daily in cycles of 21 days until unacceptable toxicity, tumor progression, death, withdrawal from the study or investigator's discretion.
|
|---|---|---|
|
Overall Study
Death
|
33
|
13
|
|
Overall Study
Lost to Follow-up
|
3
|
1
|
|
Overall Study
Objective progression or relapse
|
1
|
1
|
|
Overall Study
Other
|
11
|
1
|
|
Overall Study
Withdrawal by Subject
|
1
|
0
|
|
Overall Study
Completed post-treatment follow-up
|
1
|
0
|
Baseline Characteristics
PF-00299804 As A Single Agent, In Patients With Advanced Non-Small Cell Lung Cancer Who Have Failed Chemotherapy And Erlotinib
Baseline characteristics by cohort
| Measure |
PF-00299804 (Adenocarcinoma Histology)
n=50 Participants
Participants with adenocarcinoma histology received PF-00299804 tablet 45 milligram (mg) orally once daily in cycles of 21 days until unacceptable toxicity, tumor progression, death, withdrawal from the study or investigator's discretion.
|
PF-00299804 (Non-adenocarcinoma Histology)
n=16 Participants
Participants with non-adenocarcinoma histology received PF-00299804 tablet 45 mg orally once daily in cycles of 21 days until unacceptable toxicity, tumor progression, death, withdrawal from the study or investigator's discretion.
|
Total
n=66 Participants
Total of all reporting groups
|
|---|---|---|---|
|
Age, Continuous
|
60.7 years
STANDARD_DEVIATION 9.3 • n=5 Participants
|
65.0 years
STANDARD_DEVIATION 10.7 • n=7 Participants
|
61.7 years
STANDARD_DEVIATION 9.7 • n=5 Participants
|
|
Sex: Female, Male
Female
|
35 Participants
n=5 Participants
|
2 Participants
n=7 Participants
|
37 Participants
n=5 Participants
|
|
Sex: Female, Male
Male
|
15 Participants
n=5 Participants
|
14 Participants
n=7 Participants
|
29 Participants
n=5 Participants
|
PRIMARY outcome
Timeframe: Baseline, end of every even-numbered cycle up to end of treatment (Day 936)Population: Response-evaluable population included all enrolled participants who received at least 1 dose of study treatment, with adequate baseline tumor assessment and at least 1 on-study tumor assessment after the first dosing.
BOR:best response recorded from treatment start until disease progression as per Response Evaluation Criteria in Solid Tumors (RECIST). Complete Response: disappearance of all lesions. Partial Response (PR):greater than or equal to (\>=)30% decrease in sum of longest diameters (SLDs) of target lesions (TLs) taking as reference baseline SLD. Progressive disease (PD):\>=20% increase in SLD of TLs taking as reference smallest SLD since treatment start, or appearance of \>=1 new lesion. Stable disease:neither shrinkage for PR nor increase for PD taking as reference smallest SLD since treatment start.
Outcome measures
| Measure |
PF-00299804 (Adenocarcinoma Histology)
n=42 Participants
Participants with adenocarcinoma histology received PF-00299804 tablet 45 milligram (mg) orally once daily in cycles of 21 days until unacceptable toxicity, tumor progression, death, withdrawal from the study or investigator's discretion.
|
PF-00299804 (Non-adenocarcinoma Histology)
Participants with non-adenocarcinoma histology received PF-00299804 tablet 45 mg orally once daily in cycles of 21 days until unacceptable toxicity, tumor progression, death, withdrawal from the study or investigator's discretion.
|
|---|---|---|
|
Best Overall Response (BOR) in Participants With Adenocarcinoma Histology
Complete response
|
0 Participants
|
—
|
|
Best Overall Response (BOR) in Participants With Adenocarcinoma Histology
Partial response
|
2 Participants
|
—
|
|
Best Overall Response (BOR) in Participants With Adenocarcinoma Histology
Stable or No response
|
28 Participants
|
—
|
|
Best Overall Response (BOR) in Participants With Adenocarcinoma Histology
Objective progression
|
12 Participants
|
—
|
|
Best Overall Response (BOR) in Participants With Adenocarcinoma Histology
Indeterminate
|
0 Participants
|
—
|
SECONDARY outcome
Timeframe: Baseline, end of every even-numbered cycle up to end of treatment (Day 936)Population: Response-evaluable population included all enrolled participants who received at least 1 dose of study treatment, with adequate baseline tumor assessment and at least 1 on-study tumor assessment after the first dosing.
BOR: best response recorded from treatment start until disease progression as per RECIST. Complete Response: disappearance of all lesions. PR: \>=30% decrease in SLDs of TLs taking as reference baseline SLD. PD: \>=20% increase in SLD of TLs taking as reference smallest SLD since treatment start, or appearance of \>=1 new lesion. Stable disease: neither shrinkage for PR nor increase for PD taking as reference smallest SLD since treatment start.
Outcome measures
| Measure |
PF-00299804 (Adenocarcinoma Histology)
n=16 Participants
Participants with adenocarcinoma histology received PF-00299804 tablet 45 milligram (mg) orally once daily in cycles of 21 days until unacceptable toxicity, tumor progression, death, withdrawal from the study or investigator's discretion.
|
PF-00299804 (Non-adenocarcinoma Histology)
Participants with non-adenocarcinoma histology received PF-00299804 tablet 45 mg orally once daily in cycles of 21 days until unacceptable toxicity, tumor progression, death, withdrawal from the study or investigator's discretion.
|
|---|---|---|
|
Best Overall Response (BOR) in Participants With Non-Adenocarcinoma Histology
Complete response
|
0 Participants
|
—
|
|
Best Overall Response (BOR) in Participants With Non-Adenocarcinoma Histology
Partial response
|
1 Participants
|
—
|
|
Best Overall Response (BOR) in Participants With Non-Adenocarcinoma Histology
Stable or no response
|
8 Participants
|
—
|
|
Best Overall Response (BOR) in Participants With Non-Adenocarcinoma Histology
Objective progression
|
7 Participants
|
—
|
|
Best Overall Response (BOR) in Participants With Non-Adenocarcinoma Histology
Indeterminate
|
0 Participants
|
—
|
SECONDARY outcome
Timeframe: Baseline, end of every even-numbered cycle up to end of treatment (Day 936)Population: DR was calculated for the subgroup of participants from the response-evaluable population, with a confirmed objective tumor response (CR or PR).
Time in weeks from the first documentation of objective tumor response to objective tumor progression or death due to any cancer. Duration of tumor response was calculated as (the date of the first documentation of objective tumor progression or death due to cancer minus the date of the first CR or PR that was subsequently confirmed plus 1) divided by 7. DR was calculated for the subgroup of participants with a confirmed objective tumor response.
Outcome measures
| Measure |
PF-00299804 (Adenocarcinoma Histology)
n=2 Participants
Participants with adenocarcinoma histology received PF-00299804 tablet 45 milligram (mg) orally once daily in cycles of 21 days until unacceptable toxicity, tumor progression, death, withdrawal from the study or investigator's discretion.
|
PF-00299804 (Non-adenocarcinoma Histology)
n=1 Participants
Participants with non-adenocarcinoma histology received PF-00299804 tablet 45 mg orally once daily in cycles of 21 days until unacceptable toxicity, tumor progression, death, withdrawal from the study or investigator's discretion.
|
|---|---|---|
|
Duration of Response (DR)
|
45.2 weeks
Interval 24.1 to 66.3
|
12.1 weeks
95% confidence interval was not estimable since only one participant was evaluable.
|
SECONDARY outcome
Timeframe: Up to 6 months after the start of study medicationPopulation: As-enrolled population included all participants who were enrolled in the study.
Probability of being event free (event defined as PD or death due to any cause) at 6 months after the first dose of study treatment. PFS was defined as the time from the first dosing date to the date of first documentation of progression or death due to any cause, whichever occurs first. PFS was calculated as (first event date (if not reached, censored at the last known event-free date) minus first dosing date plus 1). Documentation of progression was determined from objective disease assessment based on RECIST v1.0 criteria. PD was defined as at least a 20% increase in the sum of the longest diameters of the target lesions taking as a reference the smallest sum of the longest diameters recorded since treated started or the appearance of 1 or more new lesions.
Outcome measures
| Measure |
PF-00299804 (Adenocarcinoma Histology)
n=50 Participants
Participants with adenocarcinoma histology received PF-00299804 tablet 45 milligram (mg) orally once daily in cycles of 21 days until unacceptable toxicity, tumor progression, death, withdrawal from the study or investigator's discretion.
|
PF-00299804 (Non-adenocarcinoma Histology)
n=16 Participants
Participants with non-adenocarcinoma histology received PF-00299804 tablet 45 mg orally once daily in cycles of 21 days until unacceptable toxicity, tumor progression, death, withdrawal from the study or investigator's discretion.
|
|---|---|---|
|
Percent Probability of Progression-free Survival (PFS) at Month 6
|
24.3 percent chance of being event-free
Interval 12.4 to 38.4
|
8.0 percent chance of being event-free
Interval 0.5 to 29.8
|
SECONDARY outcome
Timeframe: Months 6, 12Population: As-enrolled population included all participants who were enrolled in the study.
Probability of being alive at 6 and 12 months after the first dose of study medication.
Outcome measures
| Measure |
PF-00299804 (Adenocarcinoma Histology)
n=50 Participants
Participants with adenocarcinoma histology received PF-00299804 tablet 45 milligram (mg) orally once daily in cycles of 21 days until unacceptable toxicity, tumor progression, death, withdrawal from the study or investigator's discretion.
|
PF-00299804 (Non-adenocarcinoma Histology)
n=16 Participants
Participants with non-adenocarcinoma histology received PF-00299804 tablet 45 mg orally once daily in cycles of 21 days until unacceptable toxicity, tumor progression, death, withdrawal from the study or investigator's discretion.
|
|---|---|---|
|
Percent Probability of Overall Survival at Months 6 and 12
Month 6
|
71.5 percent chance of being alive
Interval 56.7 to 82.1
|
50.0 percent chance of being alive
Interval 24.5 to 71.0
|
|
Percent Probability of Overall Survival at Months 6 and 12
Month 12
|
46.3 percent chance of being alive
Interval 31.4 to 59.9
|
21.9 percent chance of being alive
Interval 5.6 to 44.9
|
SECONDARY outcome
Timeframe: 0.5-2, 3-5, 6-8, 22-26 hours post dose on Day 1 of Cycle 1Population: PK concentration population included all enrolled participants who received at least 1 dose of study treatment and had at least 1 measured plasma concentration. Here, 'N' (overall number of participants analyzed) signifies those participants who were evaluable for the measure.
The pharmacokinetic (PK) samples collected between 22-26 hours post dose on Day 1 of Cycle 1 were within the pre-specified time window for the 24-hour post dose sample and were used for calculation of AUC (0-24) on Day 1 of Cycle 1.
Outcome measures
| Measure |
PF-00299804 (Adenocarcinoma Histology)
n=49 Participants
Participants with adenocarcinoma histology received PF-00299804 tablet 45 milligram (mg) orally once daily in cycles of 21 days until unacceptable toxicity, tumor progression, death, withdrawal from the study or investigator's discretion.
|
PF-00299804 (Non-adenocarcinoma Histology)
n=13 Participants
Participants with non-adenocarcinoma histology received PF-00299804 tablet 45 mg orally once daily in cycles of 21 days until unacceptable toxicity, tumor progression, death, withdrawal from the study or investigator's discretion.
|
|---|---|---|
|
Area Under the Curve From Time Zero to 24 Hours [AUC (0-24)]
|
390.8 nanogram*hour per milliliter (ng*hr/mL)
Standard Deviation 165.24
|
397.9 nanogram*hour per milliliter (ng*hr/mL)
Standard Deviation 258.11
|
SECONDARY outcome
Timeframe: 0.5-2, 3-5, 6-8, 22-26 hours post dose on Day 1 of Cycle 1Population: PK concentration population included all enrolled participants who received at least 1 dose of study treatment and had at least 1 measured plasma concentration. Here, 'N' signifies those participants who were evaluable for the measure.
Outcome measures
| Measure |
PF-00299804 (Adenocarcinoma Histology)
n=49 Participants
Participants with adenocarcinoma histology received PF-00299804 tablet 45 milligram (mg) orally once daily in cycles of 21 days until unacceptable toxicity, tumor progression, death, withdrawal from the study or investigator's discretion.
|
PF-00299804 (Non-adenocarcinoma Histology)
n=13 Participants
Participants with non-adenocarcinoma histology received PF-00299804 tablet 45 mg orally once daily in cycles of 21 days until unacceptable toxicity, tumor progression, death, withdrawal from the study or investigator's discretion.
|
|---|---|---|
|
Maximum Observed Plasma Concentration (Cmax)
|
22.61 nanogram per milliliter
Standard Deviation 10.315
|
25.49 nanogram per milliliter
Standard Deviation 22.533
|
SECONDARY outcome
Timeframe: 0.5-2, 3-5, 6-8, 22-26 hours post dose on Day 1 of Cycle 1Population: PK concentration population included all enrolled participants who received at least 1 dose of study treatment and had at least 1 measured plasma concentration. Here, 'N' signifies those participants who were evaluable for the measure.
Outcome measures
| Measure |
PF-00299804 (Adenocarcinoma Histology)
n=49 Participants
Participants with adenocarcinoma histology received PF-00299804 tablet 45 milligram (mg) orally once daily in cycles of 21 days until unacceptable toxicity, tumor progression, death, withdrawal from the study or investigator's discretion.
|
PF-00299804 (Non-adenocarcinoma Histology)
n=13 Participants
Participants with non-adenocarcinoma histology received PF-00299804 tablet 45 mg orally once daily in cycles of 21 days until unacceptable toxicity, tumor progression, death, withdrawal from the study or investigator's discretion.
|
|---|---|---|
|
Time to Reach Maximum Observed Plasma Concentration (Tmax)
|
6.08 hours
Interval 3.0 to 25.1
|
6.17 hours
Interval 5.0 to 25.7
|
SECONDARY outcome
Timeframe: Baseline [pre-dose on Cycle 1 Day 1 (C1D1)], then pre-dose on Day 1 of each cycle, end of treatment (Day 936)Population: The pharmacodynamic population was defined as members of the ITT (as enrolled) population who had baseline samples submitted per Institutional Review Board (IRB) / Independent Ethics Committee (IEC) approval and participant consent. Here, 'number analyzed' signifies participants evaluable at each time point for each arm respectively.
Human epidermal growth factor receptor 2 (HER2) is a transmembrane protein that plays a pivotal role in growth factor signal transduction and epidermal growth factor receptor (EGFR) is a cell surface protein that binds to epidermal growth factor. Levels of the HER-2 and EGFR extracellular domains in serum were assessed by enzyme-linked immunosorbent assay (ELISA).
Outcome measures
| Measure |
PF-00299804 (Adenocarcinoma Histology)
n=48 Participants
Participants with adenocarcinoma histology received PF-00299804 tablet 45 milligram (mg) orally once daily in cycles of 21 days until unacceptable toxicity, tumor progression, death, withdrawal from the study or investigator's discretion.
|
PF-00299804 (Non-adenocarcinoma Histology)
n=14 Participants
Participants with non-adenocarcinoma histology received PF-00299804 tablet 45 mg orally once daily in cycles of 21 days until unacceptable toxicity, tumor progression, death, withdrawal from the study or investigator's discretion.
|
|---|---|---|
|
Human Epidermal Growth Factor-2 (HER-2) and Epidermal Growth Factor Receptor (EGFR) Levels in Serum
EGFR: C1D1
|
51.25 ng/mL
Standard Deviation 14.86
|
57.28 ng/mL
Standard Deviation 15.36
|
|
Human Epidermal Growth Factor-2 (HER-2) and Epidermal Growth Factor Receptor (EGFR) Levels in Serum
EGFR: C5D1
|
45.35 ng/mL
Standard Deviation 11.32
|
51.2 ng/mL
Standard Deviation 9.76
|
|
Human Epidermal Growth Factor-2 (HER-2) and Epidermal Growth Factor Receptor (EGFR) Levels in Serum
EGFR: C6D1
|
48.71 ng/mL
Standard Deviation 12.01
|
66.52 ng/mL
Standard Deviation 20.19
|
|
Human Epidermal Growth Factor-2 (HER-2) and Epidermal Growth Factor Receptor (EGFR) Levels in Serum
EGFR: C7D1
|
52.85 ng/mL
Standard Deviation 15.6
|
44.29 ng/mL
Standard Deviation 9.55
|
|
Human Epidermal Growth Factor-2 (HER-2) and Epidermal Growth Factor Receptor (EGFR) Levels in Serum
EGFR: C8D1
|
50.27 ng/mL
Standard Deviation 17.05
|
55.93 ng/mL
Standard Deviation NA
Standard deviation was not estimable since only one participant was evaluable.
|
|
Human Epidermal Growth Factor-2 (HER-2) and Epidermal Growth Factor Receptor (EGFR) Levels in Serum
EGFR: C9D1
|
50.68 ng/mL
Standard Deviation 11.41
|
—
|
|
Human Epidermal Growth Factor-2 (HER-2) and Epidermal Growth Factor Receptor (EGFR) Levels in Serum
EGFR: C10D1
|
50.45 ng/mL
Standard Deviation 11.58
|
—
|
|
Human Epidermal Growth Factor-2 (HER-2) and Epidermal Growth Factor Receptor (EGFR) Levels in Serum
HER2: C2D1
|
8.2 ng/mL
Standard Deviation 3.28
|
9.39 ng/mL
Standard Deviation 9.18
|
|
Human Epidermal Growth Factor-2 (HER-2) and Epidermal Growth Factor Receptor (EGFR) Levels in Serum
HER2: C4D1
|
7.22 ng/mL
Standard Deviation 2.25
|
6.6 ng/mL
Standard Deviation 2.44
|
|
Human Epidermal Growth Factor-2 (HER-2) and Epidermal Growth Factor Receptor (EGFR) Levels in Serum
EGFR: C2D1
|
45.89 ng/mL
Standard Deviation 12.42
|
51.05 ng/mL
Standard Deviation 11.35
|
|
Human Epidermal Growth Factor-2 (HER-2) and Epidermal Growth Factor Receptor (EGFR) Levels in Serum
EGFR: C3D1
|
44.91 ng/mL
Standard Deviation 11.43
|
46.79 ng/mL
Standard Deviation 7.64
|
|
Human Epidermal Growth Factor-2 (HER-2) and Epidermal Growth Factor Receptor (EGFR) Levels in Serum
EGFR: C4D1
|
46.26 ng/mL
Standard Deviation 11.7
|
46.72 ng/mL
Standard Deviation 9.01
|
|
Human Epidermal Growth Factor-2 (HER-2) and Epidermal Growth Factor Receptor (EGFR) Levels in Serum
HER2: C1D1
|
9.69 ng/mL
Standard Deviation 4.18
|
9.57 ng/mL
Standard Deviation 10.27
|
|
Human Epidermal Growth Factor-2 (HER-2) and Epidermal Growth Factor Receptor (EGFR) Levels in Serum
HER2: C3D1
|
7.21 ng/mL
Standard Deviation 2.31
|
6.46 ng/mL
Standard Deviation 2.92
|
|
Human Epidermal Growth Factor-2 (HER-2) and Epidermal Growth Factor Receptor (EGFR) Levels in Serum
HER2: C5D1
|
7.02 ng/mL
Standard Deviation 1.8
|
8.38 ng/mL
Standard Deviation 3.54
|
|
Human Epidermal Growth Factor-2 (HER-2) and Epidermal Growth Factor Receptor (EGFR) Levels in Serum
HER2: C6D1
|
7.74 ng/mL
Standard Deviation 4.55
|
9.9 ng/mL
Standard Deviation 7.34
|
|
Human Epidermal Growth Factor-2 (HER-2) and Epidermal Growth Factor Receptor (EGFR) Levels in Serum
HER2: C7D1
|
6.95 ng/mL
Standard Deviation 2.46
|
6.7 ng/mL
Standard Deviation 0.42
|
|
Human Epidermal Growth Factor-2 (HER-2) and Epidermal Growth Factor Receptor (EGFR) Levels in Serum
HER2: C8D1
|
6.61 ng/mL
Standard Deviation 2.95
|
11.7 ng/mL
Standard Deviation NA
Standard deviation was not estimable since only one participant was evaluable.
|
|
Human Epidermal Growth Factor-2 (HER-2) and Epidermal Growth Factor Receptor (EGFR) Levels in Serum
HER2: C9D1
|
10.23 ng/mL
Standard Deviation 11.66
|
—
|
|
Human Epidermal Growth Factor-2 (HER-2) and Epidermal Growth Factor Receptor (EGFR) Levels in Serum
HER2: C10D1
|
6.00 ng/mL
Standard Deviation 2.67
|
—
|
SECONDARY outcome
Timeframe: ScreeningPopulation: As-enrolled population included all participants who were enrolled in the study.
HER-family is a family of transmembrane protein that plays a pivotal role in growth factor signal transduction and Kirsten Rat Sarcoma (KRAS) gene is an oncogene that encodes a small guanosine triphosphatase (GTPase) transductor protein called KRAS. The mutation status of HER and KRAS genes in tumor DNA present in plasma was determined using a polymerase chain reaction (PCR)-based assay. The gene that is most common in a particular natural population is known as the wild type. Any form of the gene other than the wild type is known as a mutant form. Number of participants with HER-Family and KRAS gene mutation were classified as: wild type, mutant and unknown.
Outcome measures
| Measure |
PF-00299804 (Adenocarcinoma Histology)
n=50 Participants
Participants with adenocarcinoma histology received PF-00299804 tablet 45 milligram (mg) orally once daily in cycles of 21 days until unacceptable toxicity, tumor progression, death, withdrawal from the study or investigator's discretion.
|
PF-00299804 (Non-adenocarcinoma Histology)
n=16 Participants
Participants with non-adenocarcinoma histology received PF-00299804 tablet 45 mg orally once daily in cycles of 21 days until unacceptable toxicity, tumor progression, death, withdrawal from the study or investigator's discretion.
|
|---|---|---|
|
Number of Participants With Human Epidermal Growth Factor Family (HER-Family) and Kirsten Rat Sarcoma (KRAS) Gene Mutation Status From Free Tumor Deoxy- Ribonucleic Acid (DNA) in Blood at Screening
KRAS mutation: Unknown
|
11 Participants
|
1 Participants
|
|
Number of Participants With Human Epidermal Growth Factor Family (HER-Family) and Kirsten Rat Sarcoma (KRAS) Gene Mutation Status From Free Tumor Deoxy- Ribonucleic Acid (DNA) in Blood at Screening
HER-2 mutation: Wild-type
|
29 Participants
|
13 Participants
|
|
Number of Participants With Human Epidermal Growth Factor Family (HER-Family) and Kirsten Rat Sarcoma (KRAS) Gene Mutation Status From Free Tumor Deoxy- Ribonucleic Acid (DNA) in Blood at Screening
KRAS mutation: Wild-type
|
39 Participants
|
15 Participants
|
|
Number of Participants With Human Epidermal Growth Factor Family (HER-Family) and Kirsten Rat Sarcoma (KRAS) Gene Mutation Status From Free Tumor Deoxy- Ribonucleic Acid (DNA) in Blood at Screening
KRAS mutation: Mutant
|
0 Participants
|
0 Participants
|
|
Number of Participants With Human Epidermal Growth Factor Family (HER-Family) and Kirsten Rat Sarcoma (KRAS) Gene Mutation Status From Free Tumor Deoxy- Ribonucleic Acid (DNA) in Blood at Screening
HER-2 mutation: Mutant
|
0 Participants
|
0 Participants
|
|
Number of Participants With Human Epidermal Growth Factor Family (HER-Family) and Kirsten Rat Sarcoma (KRAS) Gene Mutation Status From Free Tumor Deoxy- Ribonucleic Acid (DNA) in Blood at Screening
HER-2 mutation: Unknown
|
21 Participants
|
3 Participants
|
SECONDARY outcome
Timeframe: Baseline (C1D1), C2D1 thereafter every subsequent cycle up to C43Population: As-enrolled population included all participants who were enrolled in the study. Here, 'N' signifies those participants who were evaluable for the measure and 'number analyzed' signifies participants evaluable at each time point for each arm respectively.
EORTC QLQ-C30: included functional scales (physical, role, cognitive, emotional, and social), global health status (GHS), symptom scales (fatigue, pain, nausea/vomiting), and single items (dyspnoea, appetite loss, insomnia, constipation/diarrhea, and financial difficulties). Most questions used 4- point scale (1 'Not at All' to 4 'Very Much'); 2 questions used 7-point scale (1 'Very Poor' to 7 'Excellent'). Scores averaged, transformed to 0-100 scale; higher score=better level of functioning or greater degree of symptoms.
Outcome measures
| Measure |
PF-00299804 (Adenocarcinoma Histology)
n=50 Participants
Participants with adenocarcinoma histology received PF-00299804 tablet 45 milligram (mg) orally once daily in cycles of 21 days until unacceptable toxicity, tumor progression, death, withdrawal from the study or investigator's discretion.
|
PF-00299804 (Non-adenocarcinoma Histology)
n=15 Participants
Participants with non-adenocarcinoma histology received PF-00299804 tablet 45 mg orally once daily in cycles of 21 days until unacceptable toxicity, tumor progression, death, withdrawal from the study or investigator's discretion.
|
|---|---|---|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Core-30 (EORTC QLQ- C30) Score
C27D1: Emotional Functioning
|
100.00 units on a scale
Standard Deviation NA
Standard deviation was not estimable since only one participant was evaluable.
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Core-30 (EORTC QLQ- C30) Score
C27D1: Cognitive Functioning
|
100.00 units on a scale
Standard Deviation NA
Standard deviation was not estimable since only one participant was evaluable.
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Core-30 (EORTC QLQ- C30) Score
C27D1: Social Functioning
|
100.00 units on a scale
Standard Deviation NA
Standard deviation was not estimable since only one participant was evaluable.
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Core-30 (EORTC QLQ- C30) Score
C27D1: Dyspnoea
|
0.00 units on a scale
Standard Deviation NA
Standard deviation was not estimable since only one participant was evaluable.
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Core-30 (EORTC QLQ- C30) Score
C27D1: Insomnia
|
0.00 units on a scale
Standard Deviation NA
Standard deviation was not estimable since only one participant was evaluable.
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Core-30 (EORTC QLQ- C30) Score
C1D1: Role functioning
|
72.67 units on a scale
Standard Deviation 33.46
|
74.44 units on a scale
Standard Deviation 32.04
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Core-30 (EORTC QLQ- C30) Score
C1D1: Emotional Functioning
|
77.72 units on a scale
Standard Deviation 23.87
|
77.22 units on a scale
Standard Deviation 16.51
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Core-30 (EORTC QLQ- C30) Score
C1D1: Cognitive Functioning
|
81.33 units on a scale
Standard Deviation 24.89
|
76.67 units on a scale
Standard Deviation 28.73
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Core-30 (EORTC QLQ- C30) Score
C1D1: Social Functioning
|
76.33 units on a scale
Standard Deviation 30.69
|
67.78 units on a scale
Standard Deviation 26.33
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Core-30 (EORTC QLQ- C30) Score
C1D1: Fatigue
|
36.44 units on a scale
Standard Deviation 25.99
|
44.44 units on a scale
Standard Deviation 26.89
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Core-30 (EORTC QLQ- C30) Score
C1D1: Nausea, vomiting
|
10.33 units on a scale
Standard Deviation 18.10
|
10.00 units on a scale
Standard Deviation 17.59
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Core-30 (EORTC QLQ- C30) Score
C1D1: Dyspnoea
|
30.00 units on a scale
Standard Deviation 31.77
|
20.00 units on a scale
Standard Deviation 27.60
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Core-30 (EORTC QLQ- C30) Score
C1D1: Insomnia
|
28.00 units on a scale
Standard Deviation 31.12
|
35.56 units on a scale
Standard Deviation 34.43
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Core-30 (EORTC QLQ- C30) Score
C1D1: Appetite loss
|
22.00 units on a scale
Standard Deviation 30.57
|
31.11 units on a scale
Standard Deviation 29.46
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Core-30 (EORTC QLQ- C30) Score
C1D1: Constipation
|
16.00 units on a scale
Standard Deviation 27.14
|
24.44 units on a scale
Standard Deviation 32.04
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Core-30 (EORTC QLQ- C30) Score
C1D1: Diarrhea
|
8.00 units on a scale
Standard Deviation 15.88
|
4.44 units on a scale
Standard Deviation 11.73
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Core-30 (EORTC QLQ- C30) Score
C2D1: GHS
|
63.83 units on a scale
Standard Deviation 24.64
|
63.46 units on a scale
Standard Deviation 17.19
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Core-30 (EORTC QLQ- C30) Score
C2D1: Nausea, vomiting
|
8.71 units on a scale
Standard Deviation 12.18
|
6.41 units on a scale
Standard Deviation 10.84
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Core-30 (EORTC QLQ- C30) Score
C2D1: Insomnia
|
19.70 units on a scale
Standard Deviation 28.14
|
17.95 units on a scale
Standard Deviation 32.25
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Core-30 (EORTC QLQ- C30) Score
C2D1: Appetite loss
|
31.82 units on a scale
Standard Deviation 34.44
|
38.46 units on a scale
Standard Deviation 35.61
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Core-30 (EORTC QLQ- C30) Score
C2D1: Constipation
|
12.88 units on a scale
Standard Deviation 24.08
|
10.26 units on a scale
Standard Deviation 21.01
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Core-30 (EORTC QLQ- C30) Score
C3D1: Physical functioning
|
79.15 units on a scale
Standard Deviation 21.59
|
62.22 units on a scale
Standard Deviation 30.66
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Core-30 (EORTC QLQ- C30) Score
C3D1: Dyspnoea
|
24.56 units on a scale
Standard Deviation 32.59
|
22.22 units on a scale
Standard Deviation 21.71
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Core-30 (EORTC QLQ- C30) Score
C3D1: Insomnia
|
21.37 units on a scale
Standard Deviation 30.09
|
27.78 units on a scale
Standard Deviation 39.78
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Core-30 (EORTC QLQ- C30) Score
C3D1: Appetite loss
|
38.46 units on a scale
Standard Deviation 36.30
|
44.44 units on a scale
Standard Deviation 38.49
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Core-30 (EORTC QLQ- C30) Score
C3D1: Constipation
|
9.17 units on a scale
Standard Deviation 21.33
|
25.00 units on a scale
Standard Deviation 35.18
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Core-30 (EORTC QLQ- C30) Score
C4D1: Nausea, vomiting
|
5.56 units on a scale
Standard Deviation 10.34
|
10.42 units on a scale
Standard Deviation 17.68
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Core-30 (EORTC QLQ- C30) Score
C5D1: Physical functioning
|
78.52 units on a scale
Standard Deviation 18.24
|
63.81 units on a scale
Standard Deviation 34.18
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Core-30 (EORTC QLQ- C30) Score
C5D1: Social Functioning
|
81.48 units on a scale
Standard Deviation 20.32
|
57.14 units on a scale
Standard Deviation 41.79
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Core-30 (EORTC QLQ- C30) Score
C5D1: Diarrhea
|
46.15 units on a scale
Standard Deviation 29.93
|
38.10 units on a scale
Standard Deviation 29.99
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Core-30 (EORTC QLQ- C30) Score
C5D1: Financial difficulties
|
17.28 units on a scale
Standard Deviation 23.33
|
33.33 units on a scale
Standard Deviation 38.49
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Core-30 (EORTC QLQ- C30) Score
C6D1: Cognitive Functioning
|
84.26 units on a scale
Standard Deviation 17.59
|
83.33 units on a scale
Standard Deviation 28.87
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Core-30 (EORTC QLQ- C30) Score
C6D1: Social Functioning
|
83.33 units on a scale
Standard Deviation 19.80
|
83.33 units on a scale
Standard Deviation 16.67
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Core-30 (EORTC QLQ- C30) Score
C6D1: Dyspnoea
|
20.37 units on a scale
Standard Deviation 25.92
|
13.33 units on a scale
Standard Deviation 18.26
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Core-30 (EORTC QLQ- C30) Score
C7D1: GHS
|
65.28 units on a scale
Standard Deviation 26.07
|
68.75 units on a scale
Standard Deviation 17.18
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Core-30 (EORTC QLQ- C30) Score
C7D1: Pain
|
14.29 units on a scale
Standard Deviation 21.54
|
20.83 units on a scale
Standard Deviation 20.97
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Core-30 (EORTC QLQ- C30) Score
C7D1: Dyspnoea
|
19.05 units on a scale
Standard Deviation 21.54
|
16.67 units on a scale
Standard Deviation 19.25
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Core-30 (EORTC QLQ- C30) Score
C7D1: Insomnia
|
26.19 units on a scale
Standard Deviation 32.50
|
16.67 units on a scale
Standard Deviation 19.25
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Core-30 (EORTC QLQ- C30) Score
C8D1: Role functioning
|
84.72 units on a scale
Standard Deviation 21.86
|
55.56 units on a scale
Standard Deviation 50.92
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Core-30 (EORTC QLQ- C30) Score
C8D1: Emotional Functioning
|
80.77 units on a scale
Standard Deviation 22.92
|
61.11 units on a scale
Standard Deviation 33.68
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Core-30 (EORTC QLQ- C30) Score
C8D1: Social Functioning
|
87.18 units on a scale
Standard Deviation 18.20
|
83.33 units on a scale
Standard Deviation 16.67
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Core-30 (EORTC QLQ- C30) Score
C9D1: Nausea, vomiting
|
0.00 units on a scale
Standard Deviation 0.00
|
5.56 units on a scale
Standard Deviation 9.62
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Core-30 (EORTC QLQ- C30) Score
C9D1: Pain
|
9.26 units on a scale
Standard Deviation 12.11
|
33.33 units on a scale
Standard Deviation 57.74
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Core-30 (EORTC QLQ- C30) Score
C9D1: Appetite loss
|
33.33 units on a scale
Standard Deviation 33.33
|
33.33 units on a scale
Standard Deviation 57.74
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Core-30 (EORTC QLQ- C30) Score
C9D1: Constipation
|
3.70 units on a scale
Standard Deviation 11.11
|
11.11 units on a scale
Standard Deviation 19.25
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Core-30 (EORTC QLQ- C30) Score
C9D1: Financial difficulties
|
7.41 units on a scale
Standard Deviation 14.70
|
33.33 units on a scale
Standard Deviation 57.74
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Core-30 (EORTC QLQ- C30) Score
C10D1: Pain
|
18.52 units on a scale
Standard Deviation 22.74
|
33.33 units on a scale
Standard Deviation NA
Standard deviation was not estimable since only one participant was evaluable.
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Core-30 (EORTC QLQ- C30) Score
C10D1: Appetite loss
|
33.33 units on a scale
Standard Deviation 33.33
|
0.00 units on a scale
Standard Deviation NA
Standard deviation was not estimable since only one participant was evaluable.
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Core-30 (EORTC QLQ- C30) Score
C10D1: Constipation
|
11.11 units on a scale
Standard Deviation 23.57
|
33.33 units on a scale
Standard Deviation NA
Standard deviation was not estimable since only one participant was evaluable.
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Core-30 (EORTC QLQ- C30) Score
C12D1: Emotional Functioning
|
81.94 units on a scale
Standard Deviation 30.92
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Core-30 (EORTC QLQ- C30) Score
C12D1: Cognitive Functioning
|
75.00 units on a scale
Standard Deviation 41.83
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Core-30 (EORTC QLQ- C30) Score
C12D1: Social Functioning
|
88.89 units on a scale
Standard Deviation 20.18
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Core-30 (EORTC QLQ- C30) Score
C12D1: Fatigue
|
25.93 units on a scale
Standard Deviation 37.62
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Core-30 (EORTC QLQ- C30) Score
C12D1: Nausea, vomiting
|
5.56 units on a scale
Standard Deviation 13.61
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Core-30 (EORTC QLQ- C30) Score
C12D1: Pain
|
13.89 units on a scale
Standard Deviation 22.15
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Core-30 (EORTC QLQ- C30) Score
C13D1: Nausea, vomiting
|
12.50 units on a scale
Standard Deviation 25.00
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Core-30 (EORTC QLQ- C30) Score
C14D1: Physical functioning
|
96.67 units on a scale
Standard Deviation 4.71
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Core-30 (EORTC QLQ- C30) Score
C14D1: Role functioning
|
100.00 units on a scale
Standard Deviation 0.00
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Core-30 (EORTC QLQ- C30) Score
C29D1: GHS
|
83.33 units on a scale
Standard Deviation NA
Standard deviation was not estimable since only one participant was evaluable.
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Core-30 (EORTC QLQ- C30) Score
C14D1: Financial difficulties
|
0.00 units on a scale
Standard Deviation 0.00
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Core-30 (EORTC QLQ- C30) Score
C15D1: GHS
|
91.67 units on a scale
Standard Deviation 11.79
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Core-30 (EORTC QLQ- C30) Score
C15D1: Physical functioning
|
96.67 units on a scale
Standard Deviation 4.71
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Core-30 (EORTC QLQ- C30) Score
C15D1: Role functioning
|
100.00 units on a scale
Standard Deviation 0.00
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Core-30 (EORTC QLQ- C30) Score
C15D1: Insomnia
|
16.67 units on a scale
Standard Deviation 23.57
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Core-30 (EORTC QLQ- C30) Score
C15D1: Appetite loss
|
0.00 units on a scale
Standard Deviation 0.00
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Core-30 (EORTC QLQ- C30) Score
C19D1: Cognitive Functioning
|
100.00 units on a scale
Standard Deviation 0.00
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Core-30 (EORTC QLQ- C30) Score
C19D1: Social Functioning
|
100.00 units on a scale
Standard Deviation 0.00
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Core-30 (EORTC QLQ- C30) Score
C19D1: Fatigue
|
22.22 units on a scale
Standard Deviation 0.00
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Core-30 (EORTC QLQ- C30) Score
C20D1: Role functioning
|
100.00 units on a scale
Standard Deviation 0.00
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Core-30 (EORTC QLQ- C30) Score
C20D1: Emotional Functioning
|
100.00 units on a scale
Standard Deviation 0.00
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Core-30 (EORTC QLQ- C30) Score
C20D1: Cognitive Functioning
|
100.00 units on a scale
Standard Deviation 0.00
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Core-30 (EORTC QLQ- C30) Score
C20D1: Dyspnoea
|
0.00 units on a scale
Standard Deviation 0.00
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Core-30 (EORTC QLQ- C30) Score
C20D1: Insomnia
|
0.00 units on a scale
Standard Deviation 0.00
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Core-30 (EORTC QLQ- C30) Score
C20D1: Appetite loss
|
0.00 units on a scale
Standard Deviation 0.00
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Core-30 (EORTC QLQ- C30) Score
C20D1: Constipation
|
0.00 units on a scale
Standard Deviation 0.00
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Core-30 (EORTC QLQ- C30) Score
C20D1: Diarrhea
|
33.33 units on a scale
Standard Deviation 0.00
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Core-30 (EORTC QLQ- C30) Score
C21D1: Appetite loss
|
0.00 units on a scale
Standard Deviation 0.00
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Core-30 (EORTC QLQ- C30) Score
C21D1: Constipation
|
0.00 units on a scale
Standard Deviation 0.00
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Core-30 (EORTC QLQ- C30) Score
C21D1: Diarrhea
|
33.33 units on a scale
Standard Deviation 0.00
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Core-30 (EORTC QLQ- C30) Score
C21D1: Financial difficulties
|
0.00 units on a scale
Standard Deviation 0.00
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Core-30 (EORTC QLQ- C30) Score
C22D1: GHS
|
83.33 units on a scale
Standard Deviation 0.00
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Core-30 (EORTC QLQ- C30) Score
C22D1: Physical functioning
|
100.00 units on a scale
Standard Deviation 0.00
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Core-30 (EORTC QLQ- C30) Score
C22D1: Dyspnoea
|
0.00 units on a scale
Standard Deviation 0.00
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Core-30 (EORTC QLQ- C30) Score
C22D1: Insomnia
|
0.00 units on a scale
Standard Deviation 0.00
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Core-30 (EORTC QLQ- C30) Score
C22D1: Appetite loss
|
0.00 units on a scale
Standard Deviation 0.00
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Core-30 (EORTC QLQ- C30) Score
C23D1: Fatigue
|
5.56 units on a scale
Standard Deviation 7.86
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Core-30 (EORTC QLQ- C30) Score
C23D1: Nausea, vomiting
|
0.00 units on a scale
Standard Deviation 0.00
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Core-30 (EORTC QLQ- C30) Score
C23D1: Pain
|
0.00 units on a scale
Standard Deviation 0.00
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Core-30 (EORTC QLQ- C30) Score
C24D1: Social Functioning
|
100.00 units on a scale
Standard Deviation 0.00
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Core-30 (EORTC QLQ- C30) Score
C24D1: Fatigue
|
5.56 units on a scale
Standard Deviation 7.86
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Core-30 (EORTC QLQ- C30) Score
C24D1: Nausea, vomiting
|
8.33 units on a scale
Standard Deviation 11.79
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Core-30 (EORTC QLQ- C30) Score
C24D1: Pain
|
0.00 units on a scale
Standard Deviation 0.00
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Core-30 (EORTC QLQ- C30) Score
C24D1: Financial difficulties
|
16.67 units on a scale
Standard Deviation 23.57
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Core-30 (EORTC QLQ- C30) Score
C25D1: GHS
|
83.33 units on a scale
Standard Deviation 0.00
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Core-30 (EORTC QLQ- C30) Score
C25D1: Physical functioning
|
100.00 units on a scale
Standard Deviation 0.00
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Core-30 (EORTC QLQ- C30) Score
C25D1: Fatigue
|
11.11 units on a scale
Standard Deviation 15.71
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Core-30 (EORTC QLQ- C30) Score
C25D1: Nausea, vomiting
|
0.00 units on a scale
Standard Deviation 0.00
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Core-30 (EORTC QLQ- C30) Score
C25D1: Pain
|
0.00 units on a scale
Standard Deviation 0.00
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Core-30 (EORTC QLQ- C30) Score
C25D1: Dyspnoea
|
0.00 units on a scale
Standard Deviation 0.00
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Core-30 (EORTC QLQ- C30) Score
C25D1: Insomnia
|
16.67 units on a scale
Standard Deviation 23.57
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Core-30 (EORTC QLQ- C30) Score
C25D1: Appetite loss
|
16.67 units on a scale
Standard Deviation 23.57
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Core-30 (EORTC QLQ- C30) Score
C25D1: Constipation
|
0.00 units on a scale
Standard Deviation 0.00
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Core-30 (EORTC QLQ- C30) Score
C25D1: Diarrhea
|
50.00 units on a scale
Standard Deviation 23.57
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Core-30 (EORTC QLQ- C30) Score
C25D1: Financial difficulties
|
16.67 units on a scale
Standard Deviation 23.57
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Core-30 (EORTC QLQ- C30) Score
C26D1: GHS
|
83.33 units on a scale
Standard Deviation NA
Standard deviation was not estimable since only one participant was evaluable.
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Core-30 (EORTC QLQ- C30) Score
C26D1: Physical functioning
|
100.00 units on a scale
Standard Deviation NA
Standard deviation was not estimable since only one participant was evaluable.
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Core-30 (EORTC QLQ- C30) Score
C26D1: Role functioning
|
66.67 units on a scale
Standard Deviation NA
Standard deviation was not estimable since only one participant was evaluable.
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Core-30 (EORTC QLQ- C30) Score
C26D1: Emotional Functioning
|
100.00 units on a scale
Standard Deviation NA
Standard deviation was not estimable since only one participant was evaluable.
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Core-30 (EORTC QLQ- C30) Score
C26D1: Cognitive Functioning
|
100.00 units on a scale
Standard Deviation NA
Standard deviation was not estimable since only one participant was evaluable.
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Core-30 (EORTC QLQ- C30) Score
C26D1: Social Functioning
|
100.00 units on a scale
Standard Deviation NA
Standard deviation was not estimable since only one participant was evaluable.
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Core-30 (EORTC QLQ- C30) Score
C26D1: Fatigue
|
0.00 units on a scale
Standard Deviation NA
Standard deviation was not estimable since only one participant was evaluable.
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Core-30 (EORTC QLQ- C30) Score
C26D1: Nausea, vomiting
|
0.00 units on a scale
Standard Deviation NA
Standard deviation was not estimable since only one participant was evaluable.
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Core-30 (EORTC QLQ- C30) Score
C26D1: Appetite loss
|
0.00 units on a scale
Standard Deviation NA
Standard deviation was not estimable since only one participant was evaluable.
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Core-30 (EORTC QLQ- C30) Score
C26D1: Constipation
|
0.00 units on a scale
Standard Deviation NA
Standard deviation was not estimable since only one participant was evaluable.
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Core-30 (EORTC QLQ- C30) Score
C26D1: Diarrhea
|
33.33 units on a scale
Standard Deviation NA
Standard deviation was not estimable since only one participant was evaluable.
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Core-30 (EORTC QLQ- C30) Score
C26D1: Financial difficulties
|
0.00 units on a scale
Standard Deviation NA
Standard deviation was not estimable since only one participant was evaluable.
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Core-30 (EORTC QLQ- C30) Score
C27D1: GHS
|
83.33 units on a scale
Standard Deviation NA
Standard deviation was not estimable since only one participant was evaluable.
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Core-30 (EORTC QLQ- C30) Score
C27D1: Physical functioning
|
100.00 units on a scale
Standard Deviation NA
Standard deviation was not estimable since only one participant was evaluable.
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Core-30 (EORTC QLQ- C30) Score
C27D1: Role functioning
|
66.67 units on a scale
Standard Deviation NA
Standard deviation was not estimable since only one participant was evaluable.
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Core-30 (EORTC QLQ- C30) Score
C29D1: Physical functioning
|
100.00 units on a scale
Standard Deviation NA
Standard deviation was not estimable since only one participant was evaluable.
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Core-30 (EORTC QLQ- C30) Score
C29D1: Role functioning
|
100.00 units on a scale
Standard Deviation NA
Standard deviation was not estimable since only one participant was evaluable.
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Core-30 (EORTC QLQ- C30) Score
C29D1: Emotional Functioning
|
100.00 units on a scale
Standard Deviation NA
Standard deviation was not estimable since only one participant was evaluable.
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Core-30 (EORTC QLQ- C30) Score
C29D1: Cognitive Functioning
|
100.00 units on a scale
Standard Deviation NA
Standard deviation was not estimable since only one participant was evaluable.
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Core-30 (EORTC QLQ- C30) Score
C29D1: Social Functioning
|
100.00 units on a scale
Standard Deviation NA
Standard deviation was not estimable since only one participant was evaluable.
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Core-30 (EORTC QLQ- C30) Score
C30D1: Financial difficulties
|
0.00 units on a scale
Standard Deviation NA
Standard deviation was not estimable since only one participant was evaluable.
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Core-30 (EORTC QLQ- C30) Score
C31D1: Financial difficulties
|
0.00 units on a scale
Standard Deviation NA
Standard deviation was not estimable since only one participant was evaluable.
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Core-30 (EORTC QLQ- C30) Score
C32D1: GHS
|
83.33 units on a scale
Standard Deviation NA
Standard deviation was not estimable since only one participant was evaluable.
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Core-30 (EORTC QLQ- C30) Score
C33D1: Financial difficulties
|
0.00 units on a scale
Standard Deviation NA
Standard deviation was not estimable since only one participant was evaluable.
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Core-30 (EORTC QLQ- C30) Score
C35D1: Physical functioning
|
100.00 units on a scale
Standard Deviation NA
Standard deviation was not estimable since only one participant was evaluable.
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Core-30 (EORTC QLQ- C30) Score
C36D1: Appetite loss
|
0.00 units on a scale
Standard Deviation NA
Standard deviation was not estimable since only one participant was evaluable.
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Core-30 (EORTC QLQ- C30) Score
C36D1: Constipation
|
0.00 units on a scale
Standard Deviation NA
Standard deviation was not estimable since only one participant was evaluable.
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Core-30 (EORTC QLQ- C30) Score
C36D1: Diarrhea
|
0.00 units on a scale
Standard Deviation NA
Standard deviation was not estimable since only one participant was evaluable.
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Core-30 (EORTC QLQ- C30) Score
C37D1: Role functioning
|
100.00 units on a scale
Standard Deviation NA
Standard deviation was not estimable since only one participant was evaluable.
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Core-30 (EORTC QLQ- C30) Score
C38D1: Physical functioning
|
100.00 units on a scale
Standard Deviation NA
Standard deviation was not estimable since only one participant was evaluable.
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Core-30 (EORTC QLQ- C30) Score
C38D1: Role functioning
|
100.00 units on a scale
Standard Deviation NA
Standard deviation was not estimable since only one participant was evaluable.
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Core-30 (EORTC QLQ- C30) Score
C40D1: Insomnia
|
0.00 units on a scale
Standard Deviation NA
Standard deviation was not estimable since only one participant was evaluable.
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Core-30 (EORTC QLQ- C30) Score
C41D1: Emotional Functioning
|
100.00 units on a scale
Standard Deviation NA
Standard deviation was not estimable since only one participant was evaluable.
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Core-30 (EORTC QLQ- C30) Score
C42D1: Emotional Functioning
|
100.00 units on a scale
Standard Deviation NA
Standard deviation was not estimable since only one participant was evaluable.
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Core-30 (EORTC QLQ- C30) Score
C43D1: Cognitive Functioning
|
100.00 units on a scale
Standard Deviation NA
Standard deviation was not estimable since only one participant was evaluable.
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Core-30 (EORTC QLQ- C30) Score
C43D1: Appetite loss
|
0.00 units on a scale
Standard Deviation NA
Standard deviation was not estimable since only one participant was evaluable.
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Core-30 (EORTC QLQ- C30) Score
C43D1: Constipation
|
0.00 units on a scale
Standard Deviation NA
Standard deviation was not estimable since only one participant was evaluable.
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Core-30 (EORTC QLQ- C30) Score
C7D1: Physical functioning
|
79.05 units on a scale
Standard Deviation 19.89
|
75.00 units on a scale
Standard Deviation 19.15
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Core-30 (EORTC QLQ- C30) Score
C7D1: Role functioning
|
80.95 units on a scale
Standard Deviation 25.20
|
70.83 units on a scale
Standard Deviation 28.46
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Core-30 (EORTC QLQ- C30) Score
C7D1: Emotional Functioning
|
75.69 units on a scale
Standard Deviation 23.15
|
87.50 units on a scale
Standard Deviation 15.96
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Core-30 (EORTC QLQ- C30) Score
C7D1: Cognitive Functioning
|
76.39 units on a scale
Standard Deviation 20.67
|
87.50 units on a scale
Standard Deviation 25.00
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Core-30 (EORTC QLQ- C30) Score
C7D1: Social Functioning
|
80.56 units on a scale
Standard Deviation 26.43
|
83.33 units on a scale
Standard Deviation 19.25
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Core-30 (EORTC QLQ- C30) Score
C7D1: Fatigue
|
34.92 units on a scale
Standard Deviation 25.08
|
27.78 units on a scale
Standard Deviation 19.25
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Core-30 (EORTC QLQ- C30) Score
C7D1: Nausea, vomiting
|
5.95 units on a scale
Standard Deviation 12.42
|
16.67 units on a scale
Standard Deviation 13.61
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Core-30 (EORTC QLQ- C30) Score
C7D1: Appetite loss
|
23.81 units on a scale
Standard Deviation 33.15
|
0.00 units on a scale
Standard Deviation 0.00
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Core-30 (EORTC QLQ- C30) Score
C43D1: Fatigue
|
0.00 units on a scale
Standard Deviation NA
Standard deviation was not estimable since only one participant was evaluable.
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Core-30 (EORTC QLQ- C30) Score
C6D1: Role functioning
|
80.56 units on a scale
Standard Deviation 20.01
|
63.33 units on a scale
Standard Deviation 41.50
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Core-30 (EORTC QLQ- C30) Score
C6D1: Emotional Functioning
|
80.09 units on a scale
Standard Deviation 20.64
|
81.67 units on a scale
Standard Deviation 22.36
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Core-30 (EORTC QLQ- C30) Score
C6D1: Fatigue
|
29.63 units on a scale
Standard Deviation 25.57
|
37.78 units on a scale
Standard Deviation 20.18
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Core-30 (EORTC QLQ- C30) Score
C31D1: GHS
|
83.33 units on a scale
Standard Deviation NA
Standard deviation was not estimable since only one participant was evaluable.
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Core-30 (EORTC QLQ- C30) Score
C31D1: Physical functioning
|
100.00 units on a scale
Standard Deviation NA
Standard deviation was not estimable since only one participant was evaluable.
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Core-30 (EORTC QLQ- C30) Score
C31D1: Role functioning
|
100.00 units on a scale
Standard Deviation NA
Standard deviation was not estimable since only one participant was evaluable.
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Core-30 (EORTC QLQ- C30) Score
C31D1: Emotional Functioning
|
100.00 units on a scale
Standard Deviation NA
Standard deviation was not estimable since only one participant was evaluable.
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Core-30 (EORTC QLQ- C30) Score
C31D1: Cognitive Functioning
|
100.00 units on a scale
Standard Deviation NA
Standard deviation was not estimable since only one participant was evaluable.
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Core-30 (EORTC QLQ- C30) Score
C31D1: Social Functioning
|
100.00 units on a scale
Standard Deviation NA
Standard deviation was not estimable since only one participant was evaluable.
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Core-30 (EORTC QLQ- C30) Score
C31D1: Fatigue
|
0.00 units on a scale
Standard Deviation NA
Standard deviation was not estimable since only one participant was evaluable.
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Core-30 (EORTC QLQ- C30) Score
C31D1: Nausea, vomiting
|
0.00 units on a scale
Standard Deviation NA
Standard deviation was not estimable since only one participant was evaluable.
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Core-30 (EORTC QLQ- C30) Score
C31D1: Pain
|
0.00 units on a scale
Standard Deviation NA
Standard deviation was not estimable since only one participant was evaluable.
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Core-30 (EORTC QLQ- C30) Score
C31D1: Dyspnoea
|
0.00 units on a scale
Standard Deviation NA
Standard deviation was not estimable since only one participant was evaluable.
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Core-30 (EORTC QLQ- C30) Score
C31D1: Insomnia
|
0.00 units on a scale
Standard Deviation NA
Standard deviation was not estimable since only one participant was evaluable.
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Core-30 (EORTC QLQ- C30) Score
C31D1: Appetite loss
|
0.00 units on a scale
Standard Deviation NA
Standard deviation was not estimable since only one participant was evaluable.
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Core-30 (EORTC QLQ- C30) Score
C31D1: Constipation
|
0.00 units on a scale
Standard Deviation NA
Standard deviation was not estimable since only one participant was evaluable.
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Core-30 (EORTC QLQ- C30) Score
C31D1: Diarrhea
|
0.00 units on a scale
Standard Deviation NA
Standard deviation was not estimable since only one participant was evaluable.
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Core-30 (EORTC QLQ- C30) Score
C32D1: Physical functioning
|
100.00 units on a scale
Standard Deviation NA
Standard deviation was not estimable since only one participant was evaluable.
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Core-30 (EORTC QLQ- C30) Score
C32D1: Role functioning
|
100.00 units on a scale
Standard Deviation NA
Standard deviation was not estimable since only one participant was evaluable.
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Core-30 (EORTC QLQ- C30) Score
C32D1: Emotional Functioning
|
100.00 units on a scale
Standard Deviation NA
Standard deviation was not estimable since only one participant was evaluable.
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Core-30 (EORTC QLQ- C30) Score
C32D1: Cognitive Functioning
|
100.00 units on a scale
Standard Deviation NA
Standard deviation was not estimable since only one participant was evaluable.
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Core-30 (EORTC QLQ- C30) Score
C32D1: Social Functioning
|
100.00 units on a scale
Standard Deviation NA
Standard deviation was not estimable since only one participant was evaluable.
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Core-30 (EORTC QLQ- C30) Score
C32D1: Fatigue
|
0.00 units on a scale
Standard Deviation NA
Standard deviation was not estimable since only one participant was evaluable.
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Core-30 (EORTC QLQ- C30) Score
C32D1: Nausea, vomiting
|
0.00 units on a scale
Standard Deviation NA
Standard deviation was not estimable since only one participant was evaluable.
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Core-30 (EORTC QLQ- C30) Score
C32D1: Pain
|
0.00 units on a scale
Standard Deviation NA
Standard deviation was not estimable since only one participant was evaluable.
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Core-30 (EORTC QLQ- C30) Score
C32D1: Dyspnoea
|
0.00 units on a scale
Standard Deviation NA
Standard deviation was not estimable since only one participant was evaluable.
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Core-30 (EORTC QLQ- C30) Score
C32D1: Insomnia
|
0.00 units on a scale
Standard Deviation NA
Standard deviation was not estimable since only one participant was evaluable.
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Core-30 (EORTC QLQ- C30) Score
C32D1: Appetite loss
|
0.00 units on a scale
Standard Deviation NA
Standard deviation was not estimable since only one participant was evaluable.
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Core-30 (EORTC QLQ- C30) Score
C32D1: Constipation
|
0.00 units on a scale
Standard Deviation NA
Standard deviation was not estimable since only one participant was evaluable.
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Core-30 (EORTC QLQ- C30) Score
C32D1: Diarrhea
|
33.33 units on a scale
Standard Deviation NA
Standard deviation was not estimable since only one participant was evaluable.
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Core-30 (EORTC QLQ- C30) Score
C32D1: Financial difficulties
|
0.00 units on a scale
Standard Deviation NA
Standard deviation was not estimable since only one participant was evaluable.
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Core-30 (EORTC QLQ- C30) Score
C33D1: GHS
|
83.33 units on a scale
Standard Deviation NA
Standard deviation was not estimable since only one participant was evaluable.
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Core-30 (EORTC QLQ- C30) Score
C33D1: Physical functioning
|
100.00 units on a scale
Standard Deviation NA
Standard deviation was not estimable since only one participant was evaluable.
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Core-30 (EORTC QLQ- C30) Score
C33D1: Role functioning
|
100.00 units on a scale
Standard Deviation NA
Standard deviation was not estimable since only one participant was evaluable.
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Core-30 (EORTC QLQ- C30) Score
C33D1: Emotional Functioning
|
100.00 units on a scale
Standard Deviation NA
Standard deviation was not estimable since only one participant was evaluable.
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Core-30 (EORTC QLQ- C30) Score
C33D1: Cognitive Functioning
|
100.00 units on a scale
Standard Deviation NA
Standard deviation was not estimable since only one participant was evaluable.
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Core-30 (EORTC QLQ- C30) Score
C33D1: Social Functioning
|
100.00 units on a scale
Standard Deviation NA
Standard deviation was not estimable since only one participant was evaluable.
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Core-30 (EORTC QLQ- C30) Score
C33D1: Fatigue
|
0.00 units on a scale
Standard Deviation NA
Standard deviation was not estimable since only one participant was evaluable.
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Core-30 (EORTC QLQ- C30) Score
C33D1: Nausea, vomiting
|
0.00 units on a scale
Standard Deviation NA
Standard deviation was not estimable since only one participant was evaluable.
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Core-30 (EORTC QLQ- C30) Score
C33D1: Pain
|
0.00 units on a scale
Standard Deviation NA
Standard deviation was not estimable since only one participant was evaluable.
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Core-30 (EORTC QLQ- C30) Score
C33D1: Dyspnoea
|
0.00 units on a scale
Standard Deviation NA
Standard deviation was not estimable since only one participant was evaluable.
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Core-30 (EORTC QLQ- C30) Score
C33D1: Insomnia
|
0.00 units on a scale
Standard Deviation NA
Standard deviation was not estimable since only one participant was evaluable.
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Core-30 (EORTC QLQ- C30) Score
C33D1: Appetite loss
|
0.00 units on a scale
Standard Deviation NA
Standard deviation was not estimable since only one participant was evaluable.
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Core-30 (EORTC QLQ- C30) Score
C33D1: Constipation
|
0.00 units on a scale
Standard Deviation NA
Standard deviation was not estimable since only one participant was evaluable.
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Core-30 (EORTC QLQ- C30) Score
C33D1: Diarrhea
|
0.00 units on a scale
Standard Deviation NA
Standard deviation was not estimable since only one participant was evaluable.
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Core-30 (EORTC QLQ- C30) Score
C34D1: GHS
|
83.33 units on a scale
Standard Deviation NA
Standard deviation was not estimable since only one participant was evaluable.
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Core-30 (EORTC QLQ- C30) Score
C34D1: Physical functioning
|
100.00 units on a scale
Standard Deviation NA
Standard deviation was not estimable since only one participant was evaluable.
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Core-30 (EORTC QLQ- C30) Score
C34D1: Role functioning
|
100.00 units on a scale
Standard Deviation NA
Standard deviation was not estimable since only one participant was evaluable.
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Core-30 (EORTC QLQ- C30) Score
C34D1: Emotional Functioning
|
100.00 units on a scale
Standard Deviation NA
Standard deviation was not estimable since only one participant was evaluable.
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Core-30 (EORTC QLQ- C30) Score
C34D1: Cognitive Functioning
|
100.00 units on a scale
Standard Deviation NA
Standard deviation was not estimable since only one participant was evaluable.
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Core-30 (EORTC QLQ- C30) Score
C34D1: Social Functioning
|
100.00 units on a scale
Standard Deviation NA
Standard deviation was not estimable since only one participant was evaluable.
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Core-30 (EORTC QLQ- C30) Score
C34D1: Fatigue
|
11.11 units on a scale
Standard Deviation NA
Standard deviation was not estimable since only one participant was evaluable.
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Core-30 (EORTC QLQ- C30) Score
C34D1: Nausea, vomiting
|
0.00 units on a scale
Standard Deviation NA
Standard deviation was not estimable since only one participant was evaluable.
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Core-30 (EORTC QLQ- C30) Score
C34D1: Pain
|
0.00 units on a scale
Standard Deviation NA
Standard deviation was not estimable since only one participant was evaluable.
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Core-30 (EORTC QLQ- C30) Score
C34D1: Dyspnoea
|
0.00 units on a scale
Standard Deviation NA
Standard deviation was not estimable since only one participant was evaluable.
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Core-30 (EORTC QLQ- C30) Score
C34D1: Insomnia
|
0.00 units on a scale
Standard Deviation NA
Standard deviation was not estimable since only one participant was evaluable.
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Core-30 (EORTC QLQ- C30) Score
C34D1: Appetite loss
|
0.00 units on a scale
Standard Deviation NA
Standard deviation was not estimable since only one participant was evaluable.
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Core-30 (EORTC QLQ- C30) Score
C34D1: Constipation
|
0.00 units on a scale
Standard Deviation NA
Standard deviation was not estimable since only one participant was evaluable.
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Core-30 (EORTC QLQ- C30) Score
C34D1: Diarrhea
|
0.00 units on a scale
Standard Deviation NA
Standard deviation was not estimable since only one participant was evaluable.
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Core-30 (EORTC QLQ- C30) Score
C34D1: Financial difficulties
|
0.00 units on a scale
Standard Deviation NA
Standard deviation was not estimable since only one participant was evaluable.
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Core-30 (EORTC QLQ- C30) Score
C35D1: GHS
|
83.33 units on a scale
Standard Deviation NA
Standard deviation was not estimable since only one participant was evaluable.
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Core-30 (EORTC QLQ- C30) Score
C35D1: Role functioning
|
100.00 units on a scale
Standard Deviation NA
Standard deviation was not estimable since only one participant was evaluable.
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Core-30 (EORTC QLQ- C30) Score
C35D1: Emotional Functioning
|
100.00 units on a scale
Standard Deviation NA
Standard deviation was not estimable since only one participant was evaluable.
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Core-30 (EORTC QLQ- C30) Score
C35D1: Cognitive Functioning
|
100.00 units on a scale
Standard Deviation NA
Standard deviation was not estimable since only one participant was evaluable.
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Core-30 (EORTC QLQ- C30) Score
C35D1: Social Functioning
|
100.00 units on a scale
Standard Deviation NA
Standard deviation was not estimable since only one participant was evaluable.
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Core-30 (EORTC QLQ- C30) Score
C35D1: Fatigue
|
0.00 units on a scale
Standard Deviation NA
Standard deviation was not estimable since only one participant was evaluable.
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Core-30 (EORTC QLQ- C30) Score
C35D1: Nausea, vomiting
|
0.00 units on a scale
Standard Deviation NA
Standard deviation was not estimable since only one participant was evaluable.
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Core-30 (EORTC QLQ- C30) Score
C35D1: Pain
|
0.00 units on a scale
Standard Deviation NA
Standard deviation was not estimable since only one participant was evaluable.
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Core-30 (EORTC QLQ- C30) Score
C35D1: Dyspnoea
|
0.00 units on a scale
Standard Deviation NA
Standard deviation was not estimable since only one participant was evaluable.
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Core-30 (EORTC QLQ- C30) Score
C35D1: Insomnia
|
0.00 units on a scale
Standard Deviation NA
Standard deviation was not estimable since only one participant was evaluable.
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Core-30 (EORTC QLQ- C30) Score
C35D1: Appetite loss
|
0.00 units on a scale
Standard Deviation NA
Standard deviation was not estimable since only one participant was evaluable.
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Core-30 (EORTC QLQ- C30) Score
C35D1: Constipation
|
0.00 units on a scale
Standard Deviation NA
Standard deviation was not estimable since only one participant was evaluable.
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Core-30 (EORTC QLQ- C30) Score
C35D1: Diarrhea
|
0.00 units on a scale
Standard Deviation NA
Standard deviation was not estimable since only one participant was evaluable.
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Core-30 (EORTC QLQ- C30) Score
C35D1: Financial difficulties
|
0.00 units on a scale
Standard Deviation NA
Standard deviation was not estimable since only one participant was evaluable.
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Core-30 (EORTC QLQ- C30) Score
C36D1: GHS
|
83.33 units on a scale
Standard Deviation NA
Standard deviation was not estimable since only one participant was evaluable.
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Core-30 (EORTC QLQ- C30) Score
C36D1: Physical functioning
|
100.00 units on a scale
Standard Deviation NA
Standard deviation was not estimable since only one participant was evaluable.
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Core-30 (EORTC QLQ- C30) Score
C36D1: Role functioning
|
100.00 units on a scale
Standard Deviation NA
Standard deviation was not estimable since only one participant was evaluable.
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Core-30 (EORTC QLQ- C30) Score
C36D1: Emotional Functioning
|
100.00 units on a scale
Standard Deviation NA
Standard deviation was not estimable since only one participant was evaluable.
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Core-30 (EORTC QLQ- C30) Score
C36D1: Cognitive Functioning
|
100.00 units on a scale
Standard Deviation NA
Standard deviation was not estimable since only one participant was evaluable.
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Core-30 (EORTC QLQ- C30) Score
C36D1: Social Functioning
|
100.00 units on a scale
Standard Deviation NA
Standard deviation was not estimable since only one participant was evaluable.
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Core-30 (EORTC QLQ- C30) Score
C36D1: Fatigue
|
0.00 units on a scale
Standard Deviation NA
Standard deviation was not estimable since only one participant was evaluable.
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Core-30 (EORTC QLQ- C30) Score
C36D1: Nausea, vomiting
|
0.00 units on a scale
Standard Deviation NA
Standard deviation was not estimable since only one participant was evaluable.
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Core-30 (EORTC QLQ- C30) Score
C36D1: Pain
|
0.00 units on a scale
Standard Deviation NA
Standard deviation was not estimable since only one participant was evaluable.
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Core-30 (EORTC QLQ- C30) Score
C36D1: Dyspnoea
|
0.00 units on a scale
Standard Deviation NA
Standard deviation was not estimable since only one participant was evaluable.
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Core-30 (EORTC QLQ- C30) Score
C36D1: Insomnia
|
0.00 units on a scale
Standard Deviation NA
Standard deviation was not estimable since only one participant was evaluable.
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Core-30 (EORTC QLQ- C30) Score
C36D1: Financial difficulties
|
0.00 units on a scale
Standard Deviation NA
Standard deviation was not estimable since only one participant was evaluable.
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Core-30 (EORTC QLQ- C30) Score
C37D1: GHS
|
83.33 units on a scale
Standard Deviation NA
Standard deviation was not estimable since only one participant was evaluable.
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Core-30 (EORTC QLQ- C30) Score
C37D1: Physical functioning
|
100.00 units on a scale
Standard Deviation NA
Standard deviation was not estimable since only one participant was evaluable.
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Core-30 (EORTC QLQ- C30) Score
C37D1: Emotional Functioning
|
100.00 units on a scale
Standard Deviation NA
Standard deviation was not estimable since only one participant was evaluable.
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Core-30 (EORTC QLQ- C30) Score
C37D1: Cognitive Functioning
|
100.00 units on a scale
Standard Deviation NA
Standard deviation was not estimable since only one participant was evaluable.
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Core-30 (EORTC QLQ- C30) Score
C37D1: Social Functioning
|
100.00 units on a scale
Standard Deviation NA
Standard deviation was not estimable since only one participant was evaluable.
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Core-30 (EORTC QLQ- C30) Score
C37D1: Fatigue
|
11.11 units on a scale
Standard Deviation NA
Standard deviation was not estimable since only one participant was evaluable.
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Core-30 (EORTC QLQ- C30) Score
C37D1: Nausea, vomiting
|
0.00 units on a scale
Standard Deviation NA
Standard deviation was not estimable since only one participant was evaluable.
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Core-30 (EORTC QLQ- C30) Score
C37D1: Pain
|
0.00 units on a scale
Standard Deviation NA
Standard deviation was not estimable since only one participant was evaluable.
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Core-30 (EORTC QLQ- C30) Score
C37D1: Dyspnoea
|
0.00 units on a scale
Standard Deviation NA
Standard deviation was not estimable since only one participant was evaluable.
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Core-30 (EORTC QLQ- C30) Score
C37D1: Insomnia
|
0.00 units on a scale
Standard Deviation NA
Standard deviation was not estimable since only one participant was evaluable.
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Core-30 (EORTC QLQ- C30) Score
C37D1: Appetite loss
|
0.00 units on a scale
Standard Deviation NA
Standard deviation was not estimable since only one participant was evaluable.
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Core-30 (EORTC QLQ- C30) Score
C37D1: Constipation
|
0.00 units on a scale
Standard Deviation NA
Standard deviation was not estimable since only one participant was evaluable.
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Core-30 (EORTC QLQ- C30) Score
C37D1: Diarrhea
|
0.00 units on a scale
Standard Deviation NA
Standard deviation was not estimable since only one participant was evaluable.
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Core-30 (EORTC QLQ- C30) Score
C37D1: Financial difficulties
|
0.00 units on a scale
Standard Deviation NA
Standard deviation was not estimable since only one participant was evaluable.
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Core-30 (EORTC QLQ- C30) Score
C38D1: GHS
|
83.33 units on a scale
Standard Deviation NA
Standard deviation was not estimable since only one participant was evaluable.
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Core-30 (EORTC QLQ- C30) Score
C38D1: Emotional Functioning
|
100.00 units on a scale
Standard Deviation NA
Standard deviation was not estimable since only one participant was evaluable.
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Core-30 (EORTC QLQ- C30) Score
C38D1: Cognitive Functioning
|
100.00 units on a scale
Standard Deviation NA
Standard deviation was not estimable since only one participant was evaluable.
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Core-30 (EORTC QLQ- C30) Score
C38D1: Social Functioning
|
100.00 units on a scale
Standard Deviation NA
Standard deviation was not estimable since only one participant was evaluable.
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Core-30 (EORTC QLQ- C30) Score
C38D1: Fatigue
|
0.00 units on a scale
Standard Deviation NA
Standard deviation was not estimable since only one participant was evaluable.
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Core-30 (EORTC QLQ- C30) Score
C38D1: Nausea, vomiting
|
0.00 units on a scale
Standard Deviation NA
Standard deviation was not estimable since only one participant was evaluable.
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Core-30 (EORTC QLQ- C30) Score
C38D1: Pain
|
0.00 units on a scale
Standard Deviation NA
Standard deviation was not estimable since only one participant was evaluable.
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Core-30 (EORTC QLQ- C30) Score
C38D1: Dyspnoea
|
0.00 units on a scale
Standard Deviation NA
Standard deviation was not estimable since only one participant was evaluable.
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Core-30 (EORTC QLQ- C30) Score
C38D1: Insomnia
|
0.00 units on a scale
Standard Deviation NA
Standard deviation was not estimable since only one participant was evaluable.
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Core-30 (EORTC QLQ- C30) Score
C38D1: Appetite loss
|
0.00 units on a scale
Standard Deviation NA
Standard deviation was not estimable since only one participant was evaluable.
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Core-30 (EORTC QLQ- C30) Score
C38D1: Constipation
|
0.00 units on a scale
Standard Deviation NA
Standard deviation was not estimable since only one participant was evaluable.
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Core-30 (EORTC QLQ- C30) Score
C38D1: Diarrhea
|
0.00 units on a scale
Standard Deviation NA
Standard deviation was not estimable since only one participant was evaluable.
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Core-30 (EORTC QLQ- C30) Score
C38D1: Financial difficulties
|
0.00 units on a scale
Standard Deviation NA
Standard deviation was not estimable since only one participant was evaluable.
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Core-30 (EORTC QLQ- C30) Score
C39D1: GHS
|
83.33 units on a scale
Standard Deviation NA
Standard deviation was not estimable since only one participant was evaluable.
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Core-30 (EORTC QLQ- C30) Score
C39D1: Physical functioning
|
100.00 units on a scale
Standard Deviation NA
Standard deviation was not estimable since only one participant was evaluable.
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Core-30 (EORTC QLQ- C30) Score
C39D1: Role functioning
|
100.00 units on a scale
Standard Deviation NA
Standard deviation was not estimable since only one participant was evaluable.
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Core-30 (EORTC QLQ- C30) Score
C39D1: Emotional Functioning
|
100.00 units on a scale
Standard Deviation NA
Standard deviation was not estimable since only one participant was evaluable.
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Core-30 (EORTC QLQ- C30) Score
C39D1: Cognitive Functioning
|
100.00 units on a scale
Standard Deviation NA
Standard deviation was not estimable since only one participant was evaluable.
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Core-30 (EORTC QLQ- C30) Score
C39D1: Social Functioning
|
100.00 units on a scale
Standard Deviation NA
Standard deviation was not estimable since only one participant was evaluable.
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Core-30 (EORTC QLQ- C30) Score
C39D1: Fatigue
|
0.00 units on a scale
Standard Deviation NA
Standard deviation was not estimable since only one participant was evaluable.
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Core-30 (EORTC QLQ- C30) Score
C39D1: Nausea, vomiting
|
0.00 units on a scale
Standard Deviation NA
Standard deviation was not estimable since only one participant was evaluable.
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Core-30 (EORTC QLQ- C30) Score
C39D1: Pain
|
0.00 units on a scale
Standard Deviation NA
Standard deviation was not estimable since only one participant was evaluable.
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Core-30 (EORTC QLQ- C30) Score
C39D1: Dyspnoea
|
0.00 units on a scale
Standard Deviation NA
Standard deviation was not estimable since only one participant was evaluable.
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Core-30 (EORTC QLQ- C30) Score
C39D1: Insomnia
|
0.00 units on a scale
Standard Deviation NA
Standard deviation was not estimable since only one participant was evaluable.
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Core-30 (EORTC QLQ- C30) Score
C39D1: Appetite loss
|
0.00 units on a scale
Standard Deviation NA
Standard deviation was not estimable since only one participant was evaluable.
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Core-30 (EORTC QLQ- C30) Score
C39D1: Constipation
|
0.00 units on a scale
Standard Deviation NA
Standard deviation was not estimable since only one participant was evaluable.
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Core-30 (EORTC QLQ- C30) Score
C39D1: Diarrhea
|
0.00 units on a scale
Standard Deviation NA
Standard deviation was not estimable since only one participant was evaluable.
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Core-30 (EORTC QLQ- C30) Score
C39D1: Financial difficulties
|
0.00 units on a scale
Standard Deviation NA
Standard deviation was not estimable since only one participant was evaluable.
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Core-30 (EORTC QLQ- C30) Score
C40D1: GHS
|
83.33 units on a scale
Standard Deviation NA
Standard deviation was not estimable since only one participant was evaluable.
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Core-30 (EORTC QLQ- C30) Score
C40D1: Physical functioning
|
100.00 units on a scale
Standard Deviation NA
Standard deviation was not estimable since only one participant was evaluable.
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Core-30 (EORTC QLQ- C30) Score
C40D1: Role functioning
|
100.00 units on a scale
Standard Deviation NA
Standard deviation was not estimable since only one participant was evaluable.
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Core-30 (EORTC QLQ- C30) Score
C40D1: Emotional Functioning
|
100.00 units on a scale
Standard Deviation NA
Standard deviation was not estimable since only one participant was evaluable.
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Core-30 (EORTC QLQ- C30) Score
C40D1: Cognitive Functioning
|
100.00 units on a scale
Standard Deviation NA
Standard deviation was not estimable since only one participant was evaluable.
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Core-30 (EORTC QLQ- C30) Score
C40D1: Social Functioning
|
100.00 units on a scale
Standard Deviation NA
Standard deviation was not estimable since only one participant was evaluable.
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Core-30 (EORTC QLQ- C30) Score
C40D1: Fatigue
|
0.00 units on a scale
Standard Deviation NA
Standard deviation was not estimable since only one participant was evaluable.
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Core-30 (EORTC QLQ- C30) Score
C40D1: Nausea, vomiting
|
0.00 units on a scale
Standard Deviation NA
Standard deviation was not estimable since only one participant was evaluable.
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Core-30 (EORTC QLQ- C30) Score
C40D1: Pain
|
0.00 units on a scale
Standard Deviation NA
Standard deviation was not estimable since only one participant was evaluable.
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Core-30 (EORTC QLQ- C30) Score
C40D1: Dyspnoea
|
0.00 units on a scale
Standard Deviation NA
Standard deviation was not estimable since only one participant was evaluable.
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Core-30 (EORTC QLQ- C30) Score
C40D1: Appetite loss
|
0.00 units on a scale
Standard Deviation NA
Standard deviation was not estimable since only one participant was evaluable.
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Core-30 (EORTC QLQ- C30) Score
C40D1: Constipation
|
0.00 units on a scale
Standard Deviation NA
Standard deviation was not estimable since only one participant was evaluable.
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Core-30 (EORTC QLQ- C30) Score
C40D1: Diarrhea
|
0.00 units on a scale
Standard Deviation NA
Standard deviation was not estimable since only one participant was evaluable.
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Core-30 (EORTC QLQ- C30) Score
C40D1: Financial difficulties
|
0.00 units on a scale
Standard Deviation NA
Standard deviation was not estimable since only one participant was evaluable.
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Core-30 (EORTC QLQ- C30) Score
C41D1: GHS
|
83.33 units on a scale
Standard Deviation NA
Standard deviation was not estimable since only one participant was evaluable.
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Core-30 (EORTC QLQ- C30) Score
C41D1: Physical functioning
|
100.00 units on a scale
Standard Deviation NA
Standard deviation was not estimable since only one participant was evaluable.
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Core-30 (EORTC QLQ- C30) Score
C41D1: Role functioning
|
100.00 units on a scale
Standard Deviation NA
Standard deviation was not estimable since only one participant was evaluable.
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Core-30 (EORTC QLQ- C30) Score
C41D1: Cognitive Functioning
|
100.00 units on a scale
Standard Deviation NA
Standard deviation was not estimable since only one participant was evaluable.
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Core-30 (EORTC QLQ- C30) Score
C41D1: Social Functioning
|
100.00 units on a scale
Standard Deviation NA
Standard deviation was not estimable since only one participant was evaluable.
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Core-30 (EORTC QLQ- C30) Score
C41D1: Fatigue
|
0.00 units on a scale
Standard Deviation NA
Standard deviation was not estimable since only one participant was evaluable.
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Core-30 (EORTC QLQ- C30) Score
C41D1: Nausea, vomiting
|
0.00 units on a scale
Standard Deviation NA
Standard deviation was not estimable since only one participant was evaluable.
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Core-30 (EORTC QLQ- C30) Score
C41D1: Pain
|
0.00 units on a scale
Standard Deviation NA
Standard deviation was not estimable since only one participant was evaluable.
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Core-30 (EORTC QLQ- C30) Score
C6D1: Nausea, vomiting
|
8.33 units on a scale
Standard Deviation 16.42
|
6.67 units on a scale
Standard Deviation 14.91
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Core-30 (EORTC QLQ- C30) Score
C41D1: Dyspnoea
|
0.00 units on a scale
Standard Deviation NA
Standard deviation was not estimable since only one participant was evaluable.
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Core-30 (EORTC QLQ- C30) Score
C41D1: Insomnia
|
0.00 units on a scale
Standard Deviation NA
Standard deviation was not estimable since only one participant was evaluable.
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Core-30 (EORTC QLQ- C30) Score
C41D1: Appetite loss
|
0.00 units on a scale
Standard Deviation NA
Standard deviation was not estimable since only one participant was evaluable.
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Core-30 (EORTC QLQ- C30) Score
C41D1: Constipation
|
0.00 units on a scale
Standard Deviation NA
Standard deviation was not estimable since only one participant was evaluable.
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Core-30 (EORTC QLQ- C30) Score
C41D1: Diarrhea
|
0.00 units on a scale
Standard Deviation NA
Standard deviation was not estimable since only one participant was evaluable.
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Core-30 (EORTC QLQ- C30) Score
C41D1: Financial difficulties
|
0.00 units on a scale
Standard Deviation NA
Standard deviation was not estimable since only one participant was evaluable.
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Core-30 (EORTC QLQ- C30) Score
C42D1: GHS
|
83.33 units on a scale
Standard Deviation NA
Standard deviation was not estimable since only one participant was evaluable.
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Core-30 (EORTC QLQ- C30) Score
C6D1: Pain
|
18.52 units on a scale
Standard Deviation 24.85
|
30.00 units on a scale
Standard Deviation 27.39
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Core-30 (EORTC QLQ- C30) Score
C42D1: Physical functioning
|
100.00 units on a scale
Standard Deviation NA
Standard deviation was not estimable since only one participant was evaluable.
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Core-30 (EORTC QLQ- C30) Score
C42D1: Role functioning
|
100.00 units on a scale
Standard Deviation NA
Standard deviation was not estimable since only one participant was evaluable.
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Core-30 (EORTC QLQ- C30) Score
C6D1: Insomnia
|
23.53 units on a scale
Standard Deviation 28.30
|
20.00 units on a scale
Standard Deviation 18.26
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Core-30 (EORTC QLQ- C30) Score
C42D1: Cognitive Functioning
|
100.00 units on a scale
Standard Deviation NA
Standard deviation was not estimable since only one participant was evaluable.
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Core-30 (EORTC QLQ- C30) Score
C42D1: Social Functioning
|
100.00 units on a scale
Standard Deviation NA
Standard deviation was not estimable since only one participant was evaluable.
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Core-30 (EORTC QLQ- C30) Score
C42D1: Fatigue
|
0.00 units on a scale
Standard Deviation NA
Standard deviation was not estimable since only one participant was evaluable.
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Core-30 (EORTC QLQ- C30) Score
C6D1: Appetite loss
|
25.93 units on a scale
Standard Deviation 37.15
|
20.00 units on a scale
Standard Deviation 44.72
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Core-30 (EORTC QLQ- C30) Score
C42D1: Nausea, vomiting
|
0.00 units on a scale
Standard Deviation NA
Standard deviation was not estimable since only one participant was evaluable.
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Core-30 (EORTC QLQ- C30) Score
C42D1: Pain
|
0.00 units on a scale
Standard Deviation NA
Standard deviation was not estimable since only one participant was evaluable.
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Core-30 (EORTC QLQ- C30) Score
C42D1: Dyspnoea
|
0.00 units on a scale
Standard Deviation NA
Standard deviation was not estimable since only one participant was evaluable.
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Core-30 (EORTC QLQ- C30) Score
C42D1: Insomnia
|
0.00 units on a scale
Standard Deviation NA
Standard deviation was not estimable since only one participant was evaluable.
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Core-30 (EORTC QLQ- C30) Score
C42D1: Appetite loss
|
0.00 units on a scale
Standard Deviation NA
Standard deviation was not estimable since only one participant was evaluable.
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Core-30 (EORTC QLQ- C30) Score
C42D1: Constipation
|
0.00 units on a scale
Standard Deviation NA
Standard deviation was not estimable since only one participant was evaluable.
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Core-30 (EORTC QLQ- C30) Score
C42D1: Diarrhea
|
0.00 units on a scale
Standard Deviation NA
Standard deviation was not estimable since only one participant was evaluable.
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Core-30 (EORTC QLQ- C30) Score
C42D1: Financial difficulties
|
0.00 units on a scale
Standard Deviation NA
Standard deviation was not estimable since only one participant was evaluable.
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Core-30 (EORTC QLQ- C30) Score
C43D1: GHS
|
83.33 units on a scale
Standard Deviation NA
Standard deviation was not estimable since only one participant was evaluable.
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Core-30 (EORTC QLQ- C30) Score
C43D1: Physical functioning
|
100.00 units on a scale
Standard Deviation NA
Standard deviation was not estimable since only one participant was evaluable.
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Core-30 (EORTC QLQ- C30) Score
C43D1: Role functioning
|
100.00 units on a scale
Standard Deviation NA
Standard deviation was not estimable since only one participant was evaluable.
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Core-30 (EORTC QLQ- C30) Score
C6D1: Constipation
|
3.70 units on a scale
Standard Deviation 10.78
|
26.67 units on a scale
Standard Deviation 43.46
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Core-30 (EORTC QLQ- C30) Score
C43D1: Emotional Functioning
|
100.00 units on a scale
Standard Deviation NA
Standard deviation was not estimable since only one participant was evaluable.
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Core-30 (EORTC QLQ- C30) Score
C43D1: Social Functioning
|
100.00 units on a scale
Standard Deviation NA
Standard deviation was not estimable since only one participant was evaluable.
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Core-30 (EORTC QLQ- C30) Score
C43D1: Nausea, vomiting
|
0.00 units on a scale
Standard Deviation NA
Standard deviation was not estimable since only one participant was evaluable.
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Core-30 (EORTC QLQ- C30) Score
C43D1: Pain
|
0.00 units on a scale
Standard Deviation NA
Standard deviation was not estimable since only one participant was evaluable.
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Core-30 (EORTC QLQ- C30) Score
C43D1: Dyspnoea
|
0.00 units on a scale
Standard Deviation NA
Standard deviation was not estimable since only one participant was evaluable.
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Core-30 (EORTC QLQ- C30) Score
C43D1: Insomnia
|
0.00 units on a scale
Standard Deviation NA
Standard deviation was not estimable since only one participant was evaluable.
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Core-30 (EORTC QLQ- C30) Score
C43D1: Diarrhea
|
0.00 units on a scale
Standard Deviation NA
Standard deviation was not estimable since only one participant was evaluable.
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Core-30 (EORTC QLQ- C30) Score
C43D1: Financial difficulties
|
0.00 units on a scale
Standard Deviation NA
Standard deviation was not estimable since only one participant was evaluable.
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Core-30 (EORTC QLQ- C30) Score
C6D1: Diarrhea
|
35.19 units on a scale
Standard Deviation 21.30
|
20.00 units on a scale
Standard Deviation 29.81
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Core-30 (EORTC QLQ- C30) Score
C6D1: Financial difficulties
|
11.11 units on a scale
Standard Deviation 19.80
|
40.0 units on a scale
Standard Deviation 43.46
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Core-30 (EORTC QLQ- C30) Score
C1D1: GHS
|
65.83 units on a scale
Standard Deviation 24.99
|
60.56 units on a scale
Standard Deviation 25.87
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Core-30 (EORTC QLQ- C30) Score
C1D1: Physical functioning
|
74.70 units on a scale
Standard Deviation 22.17
|
70.22 units on a scale
Standard Deviation 27.24
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Core-30 (EORTC QLQ- C30) Score
C1D1: Pain
|
30.33 units on a scale
Standard Deviation 32.24
|
30.00 units on a scale
Standard Deviation 30.99
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Core-30 (EORTC QLQ- C30) Score
C1D1: Financial difficulties
|
20.41 units on a scale
Standard Deviation 32.50
|
22.22 units on a scale
Standard Deviation 34.88
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Core-30 (EORTC QLQ- C30) Score
C2D1: Physical functioning
|
76.82 units on a scale
Standard Deviation 22.76
|
79.49 units on a scale
Standard Deviation 13.46
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Core-30 (EORTC QLQ- C30) Score
C2D1: Role functioning
|
73.86 units on a scale
Standard Deviation 31.00
|
82.05 units on a scale
Standard Deviation 27.61
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Core-30 (EORTC QLQ- C30) Score
C2D1: Emotional Functioning
|
79.73 units on a scale
Standard Deviation 21.89
|
82.69 units on a scale
Standard Deviation 13.38
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Core-30 (EORTC QLQ- C30) Score
C2D1: Cognitive Functioning
|
81.44 units on a scale
Standard Deviation 19.76
|
76.92 units on a scale
Standard Deviation 30.08
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Core-30 (EORTC QLQ- C30) Score
C2D1: Social Functioning
|
79.92 units on a scale
Standard Deviation 26.06
|
80.77 units on a scale
Standard Deviation 20.24
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Core-30 (EORTC QLQ- C30) Score
C2D1: Fatigue
|
38.51 units on a scale
Standard Deviation 27.25
|
41.88 units on a scale
Standard Deviation 26.89
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Core-30 (EORTC QLQ- C30) Score
C2D1: Pain
|
22.35 units on a scale
Standard Deviation 25.66
|
20.51 units on a scale
Standard Deviation 22.72
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Core-30 (EORTC QLQ- C30) Score
C2D1: Dyspnoea
|
20.45 units on a scale
Standard Deviation 25.13
|
20.51 units on a scale
Standard Deviation 16.88
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Core-30 (EORTC QLQ- C30) Score
C2D1: Diarrhea
|
54.55 units on a scale
Standard Deviation 26.99
|
38.46 units on a scale
Standard Deviation 29.96
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Core-30 (EORTC QLQ- C30) Score
C2D1: Financial difficulties
|
18.18 units on a scale
Standard Deviation 25.37
|
23.08 units on a scale
Standard Deviation 34.39
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Core-30 (EORTC QLQ- C30) Score
C3D1: GHS
|
65.21 units on a scale
Standard Deviation 21.84
|
54.86 units on a scale
Standard Deviation 25.49
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Core-30 (EORTC QLQ- C30) Score
C3D1: Role functioning
|
73.50 units on a scale
Standard Deviation 28.02
|
62.50 units on a scale
Standard Deviation 41.51
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Core-30 (EORTC QLQ- C30) Score
C3D1: Emotional Functioning
|
79.17 units on a scale
Standard Deviation 23.49
|
71.53 units on a scale
Standard Deviation 18.28
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Core-30 (EORTC QLQ- C30) Score
C3D1: Cognitive Functioning
|
80.83 units on a scale
Standard Deviation 24.33
|
73.61 units on a scale
Standard Deviation 33.68
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Core-30 (EORTC QLQ- C30) Score
C3D1: Social Functioning
|
82.92 units on a scale
Standard Deviation 21.51
|
65.28 units on a scale
Standard Deviation 24.06
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Core-30 (EORTC QLQ- C30) Score
C3D1: Fatigue
|
36.47 units on a scale
Standard Deviation 27.92
|
47.22 units on a scale
Standard Deviation 28.48
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Core-30 (EORTC QLQ- C30) Score
C3D1: Nausea, vomiting
|
14.10 units on a scale
Standard Deviation 20.43
|
15.28 units on a scale
Standard Deviation 15.01
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Core-30 (EORTC QLQ- C30) Score
C3D1: Pain
|
22.92 units on a scale
Standard Deviation 29.40
|
44.44 units on a scale
Standard Deviation 35.06
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Core-30 (EORTC QLQ- C30) Score
C3D1: Diarrhea
|
54.17 units on a scale
Standard Deviation 28.93
|
38.89 units on a scale
Standard Deviation 31.25
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Core-30 (EORTC QLQ- C30) Score
C3D1: Financial difficulties
|
17.09 units on a scale
Standard Deviation 26.35
|
33.33 units on a scale
Standard Deviation 34.82
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Core-30 (EORTC QLQ- C30) Score
C4D1: GHS
|
69.44 units on a scale
Standard Deviation 19.20
|
53.12 units on a scale
Standard Deviation 22.69
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Core-30 (EORTC QLQ- C30) Score
C4D1: Physical functioning
|
82.47 units on a scale
Standard Deviation 15.30
|
55.00 units on a scale
Standard Deviation 30.81
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Core-30 (EORTC QLQ- C30) Score
C4D1: Role functioning
|
82.10 units on a scale
Standard Deviation 23.08
|
56.25 units on a scale
Standard Deviation 33.26
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Core-30 (EORTC QLQ- C30) Score
C4D1: Emotional Functioning
|
87.04 units on a scale
Standard Deviation 14.86
|
67.71 units on a scale
Standard Deviation 24.17
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Core-30 (EORTC QLQ- C30) Score
C4D1: Cognitive Functioning
|
85.80 units on a scale
Standard Deviation 15.12
|
66.67 units on a scale
Standard Deviation 30.86
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Core-30 (EORTC QLQ- C30) Score
C4D1: Social Functioning
|
88.27 units on a scale
Standard Deviation 18.95
|
66.67 units on a scale
Standard Deviation 26.73
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Core-30 (EORTC QLQ- C30) Score
C4D1: Fatigue
|
30.04 units on a scale
Standard Deviation 21.53
|
48.61 units on a scale
Standard Deviation 29.66
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Core-30 (EORTC QLQ- C30) Score
C4D1: Pain
|
17.28 units on a scale
Standard Deviation 18.77
|
41.67 units on a scale
Standard Deviation 29.55
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Core-30 (EORTC QLQ- C30) Score
C4D1: Dyspnoea
|
18.52 units on a scale
Standard Deviation 23.27
|
33.33 units on a scale
Standard Deviation 35.63
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Core-30 (EORTC QLQ- C30) Score
C4D1: Insomnia
|
13.58 units on a scale
Standard Deviation 24.91
|
25.00 units on a scale
Standard Deviation 38.83
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Core-30 (EORTC QLQ- C30) Score
C4D1: Appetite loss
|
29.63 units on a scale
Standard Deviation 29.72
|
37.50 units on a scale
Standard Deviation 33.03
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Core-30 (EORTC QLQ- C30) Score
C4D1: Constipation
|
4.94 units on a scale
Standard Deviation 12.07
|
20.83 units on a scale
Standard Deviation 35.36
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Core-30 (EORTC QLQ- C30) Score
C4D1: Diarrhea
|
53.09 units on a scale
Standard Deviation 31.02
|
33.33 units on a scale
Standard Deviation 25.20
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Core-30 (EORTC QLQ- C30) Score
C4D1: Financial difficulties
|
8.64 units on a scale
Standard Deviation 19.81
|
25.00 units on a scale
Standard Deviation 29.55
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Core-30 (EORTC QLQ- C30) Score
C5D1: GHS
|
66.67 units on a scale
Standard Deviation 22.88
|
54.76 units on a scale
Standard Deviation 27.58
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Core-30 (EORTC QLQ- C30) Score
C5D1: Role functioning
|
77.16 units on a scale
Standard Deviation 28.17
|
40.48 units on a scale
Standard Deviation 40.66
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Core-30 (EORTC QLQ- C30) Score
C5D1: Emotional Functioning
|
80.25 units on a scale
Standard Deviation 21.33
|
77.38 units on a scale
Standard Deviation 17.82
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Core-30 (EORTC QLQ- C30) Score
C5D1: Cognitive Functioning
|
83.95 units on a scale
Standard Deviation 17.59
|
69.05 units on a scale
Standard Deviation 39.00
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Core-30 (EORTC QLQ- C30) Score
C5D1: Fatigue
|
32.51 units on a scale
Standard Deviation 24.83
|
53.70 units on a scale
Standard Deviation 34.72
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Core-30 (EORTC QLQ- C30) Score
C5D1: Nausea, vomiting
|
7.41 units on a scale
Standard Deviation 14.12
|
9.52 units on a scale
Standard Deviation 13.11
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Core-30 (EORTC QLQ- C30) Score
C5D1: Pain
|
13.58 units on a scale
Standard Deviation 21.70
|
50.00 units on a scale
Standard Deviation 38.49
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Core-30 (EORTC QLQ- C30) Score
C5D1: Dyspnoea
|
25.93 units on a scale
Standard Deviation 23.27
|
28.57 units on a scale
Standard Deviation 29.99
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Core-30 (EORTC QLQ- C30) Score
C5D1: Insomnia
|
19.75 units on a scale
Standard Deviation 26.57
|
33.33 units on a scale
Standard Deviation 43.03
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Core-30 (EORTC QLQ- C30) Score
C5D1: Appetite loss
|
35.80 units on a scale
Standard Deviation 31.93
|
33.33 units on a scale
Standard Deviation 38.49
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Core-30 (EORTC QLQ- C30) Score
C5D1: Constipation
|
7.41 units on a scale
Standard Deviation 16.88
|
19.05 units on a scale
Standard Deviation 26.23
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Core-30 (EORTC QLQ- C30) Score
C6D1: GHS
|
68.06 units on a scale
Standard Deviation 23.44
|
71.67 units on a scale
Standard Deviation 11.18
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Core-30 (EORTC QLQ- C30) Score
C6D1: Physical functioning
|
79.63 units on a scale
Standard Deviation 18.50
|
69.33 units on a scale
Standard Deviation 36.39
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Core-30 (EORTC QLQ- C30) Score
C7D1: Constipation
|
5.56 units on a scale
Standard Deviation 12.97
|
33.33 units on a scale
Standard Deviation 27.22
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Core-30 (EORTC QLQ- C30) Score
C7D1: Diarrhea
|
41.67 units on a scale
Standard Deviation 32.18
|
16.67 units on a scale
Standard Deviation 19.25
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Core-30 (EORTC QLQ- C30) Score
C7D1: Financial difficulties
|
15.15 units on a scale
Standard Deviation 22.92
|
33.33 units on a scale
Standard Deviation 47.14
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Core-30 (EORTC QLQ- C30) Score
C8D1: GHS
|
75.00 units on a scale
Standard Deviation 19.25
|
61.11 units on a scale
Standard Deviation 25.46
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Core-30 (EORTC QLQ- C30) Score
C8D1: Physical functioning
|
82.22 units on a scale
Standard Deviation 13.43
|
57.78 units on a scale
Standard Deviation 47.30
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Core-30 (EORTC QLQ- C30) Score
C8D1: Cognitive Functioning
|
75.64 units on a scale
Standard Deviation 25.11
|
94.44 units on a scale
Standard Deviation 9.62
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Core-30 (EORTC QLQ- C30) Score
C8D1: Fatigue
|
29.63 units on a scale
Standard Deviation 24.77
|
55.56 units on a scale
Standard Deviation 44.44
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Core-30 (EORTC QLQ- C30) Score
C8D1: Nausea, vomiting
|
0.00 units on a scale
Standard Deviation 0.00
|
16.67 units on a scale
Standard Deviation 16.67
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Core-30 (EORTC QLQ- C30) Score
C8D1: Pain
|
10.26 units on a scale
Standard Deviation 14.50
|
33.33 units on a scale
Standard Deviation 44.10
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Core-30 (EORTC QLQ- C30) Score
C8D1: Dyspnoea
|
22.22 units on a scale
Standard Deviation 21.71
|
11.11 units on a scale
Standard Deviation 19.25
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Core-30 (EORTC QLQ- C30) Score
C8D1: Insomnia
|
25.00 units on a scale
Standard Deviation 35.18
|
11.11 units on a scale
Standard Deviation 19.25
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Core-30 (EORTC QLQ- C30) Score
C8D1: Appetite loss
|
22.22 units on a scale
Standard Deviation 32.82
|
33.33 units on a scale
Standard Deviation 57.74
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Core-30 (EORTC QLQ- C30) Score
C8D1: Constipation
|
8.33 units on a scale
Standard Deviation 20.72
|
11.11 units on a scale
Standard Deviation 19.25
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Core-30 (EORTC QLQ- C30) Score
C8D1: Diarrhea
|
33.33 units on a scale
Standard Deviation 27.22
|
66.67 units on a scale
Standard Deviation 33.33
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Core-30 (EORTC QLQ- C30) Score
C8D1: Financial difficulties
|
10.26 units on a scale
Standard Deviation 16.01
|
33.33 units on a scale
Standard Deviation 57.74
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Core-30 (EORTC QLQ- C30) Score
C9D1: GHS
|
77.78 units on a scale
Standard Deviation 16.14
|
75.00 units on a scale
Standard Deviation 14.43
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Core-30 (EORTC QLQ- C30) Score
C9D1: Physical functioning
|
81.48 units on a scale
Standard Deviation 14.44
|
55.56 units on a scale
Standard Deviation 50.92
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Core-30 (EORTC QLQ- C30) Score
C9D1: Role functioning
|
88.89 units on a scale
Standard Deviation 16.67
|
55.56 units on a scale
Standard Deviation 50.92
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Core-30 (EORTC QLQ- C30) Score
C9D1: Emotional Functioning
|
81.48 units on a scale
Standard Deviation 22.74
|
61.11 units on a scale
Standard Deviation 25.46
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Core-30 (EORTC QLQ- C30) Score
C9D1: Cognitive Functioning
|
77.78 units on a scale
Standard Deviation 27.64
|
100.00 units on a scale
Standard Deviation 0.00
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Core-30 (EORTC QLQ- C30) Score
C9D1: Social Functioning
|
92.59 units on a scale
Standard Deviation 12.11
|
72.22 units on a scale
Standard Deviation 25.46
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Core-30 (EORTC QLQ- C30) Score
C9D1: Fatigue
|
33.33 units on a scale
Standard Deviation 28.33
|
55.56 units on a scale
Standard Deviation 50.92
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Core-30 (EORTC QLQ- C30) Score
C9D1: Dyspnoea
|
22.22 units on a scale
Standard Deviation 23.57
|
22.22 units on a scale
Standard Deviation 19.25
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Core-30 (EORTC QLQ- C30) Score
C9D1: Insomnia
|
25.93 units on a scale
Standard Deviation 27.78
|
44.44 units on a scale
Standard Deviation 50.92
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Core-30 (EORTC QLQ- C30) Score
C9D1: Diarrhea
|
25.93 units on a scale
Standard Deviation 22.22
|
33.33 units on a scale
Standard Deviation 33.33
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Core-30 (EORTC QLQ- C30) Score
C10D1: GHS
|
74.07 units on a scale
Standard Deviation 26.17
|
50.00 units on a scale
Standard Deviation NA
Standard deviation was not estimable since only one participant was evaluable.
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Core-30 (EORTC QLQ- C30) Score
C10D1: Physical functioning
|
82.96 units on a scale
Standard Deviation 14.57
|
60.00 units on a scale
Standard Deviation NA
Standard deviation was not estimable since only one participant was evaluable.
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Core-30 (EORTC QLQ- C30) Score
C10D1: Role functioning
|
79.63 units on a scale
Standard Deviation 23.24
|
66.67 units on a scale
Standard Deviation NA
Standard deviation was not estimable since only one participant was evaluable.
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Core-30 (EORTC QLQ- C30) Score
C10D1: Emotional Functioning
|
83.33 units on a scale
Standard Deviation 20.83
|
66.67 units on a scale
Standard Deviation NA
Standard deviation was not estimable since only one participant was evaluable.
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Core-30 (EORTC QLQ- C30) Score
C10D1: Cognitive Functioning
|
72.22 units on a scale
Standard Deviation 32.27
|
100.00 units on a scale
Standard Deviation NA
Standard deviation was not estimable since only one participant was evaluable.
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Core-30 (EORTC QLQ- C30) Score
C10D1: Social Functioning
|
85.19 units on a scale
Standard Deviation 19.44
|
66.67 units on a scale
Standard Deviation NA
Standard deviation was not estimable since only one participant was evaluable.
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Core-30 (EORTC QLQ- C30) Score
C10D1: Fatigue
|
35.80 units on a scale
Standard Deviation 30.32
|
66.67 units on a scale
Standard Deviation NA
Standard deviation was not estimable since only one participant was evaluable.
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Core-30 (EORTC QLQ- C30) Score
C10D1: Nausea, vomiting
|
9.26 units on a scale
Standard Deviation 27.78
|
0.00 units on a scale
Standard Deviation NA
Standard deviation was not estimable since only one participant was evaluable.
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Core-30 (EORTC QLQ- C30) Score
C10D1: Dyspnoea
|
25.93 units on a scale
Standard Deviation 32.39
|
66.67 units on a scale
Standard Deviation NA
Standard deviation was not estimable since only one participant was evaluable.
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Core-30 (EORTC QLQ- C30) Score
C10D1: Insomnia
|
33.33 units on a scale
Standard Deviation 33.33
|
0.00 units on a scale
Standard Deviation NA
Standard deviation was not estimable since only one participant was evaluable.
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Core-30 (EORTC QLQ- C30) Score
C10D1: Diarrhea
|
37.04 units on a scale
Standard Deviation 20.03
|
33.33 units on a scale
Standard Deviation NA
Standard deviation was not estimable since only one participant was evaluable.
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Core-30 (EORTC QLQ- C30) Score
C10D1: Financial difficulties
|
11.11 units on a scale
Standard Deviation 16.67
|
0.00 units on a scale
Standard Deviation NA
Standard deviation was not estimable since only one participant was evaluable.
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Core-30 (EORTC QLQ- C30) Score
C11D1: GHS
|
72.22 units on a scale
Standard Deviation 24.65
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Core-30 (EORTC QLQ- C30) Score
C11D1: Physical functioning
|
82.96 units on a scale
Standard Deviation 14.95
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Core-30 (EORTC QLQ- C30) Score
C11D1: Role functioning
|
79.63 units on a scale
Standard Deviation 20.03
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Core-30 (EORTC QLQ- C30) Score
C11D1: Emotional Functioning
|
83.33 units on a scale
Standard Deviation 22.44
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Core-30 (EORTC QLQ- C30) Score
C11D1: Cognitive Functioning
|
77.78 units on a scale
Standard Deviation 25.00
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Core-30 (EORTC QLQ- C30) Score
C11D1: Social Functioning
|
90.74 units on a scale
Standard Deviation 14.70
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Core-30 (EORTC QLQ- C30) Score
C11D1: Fatigue
|
24.69 units on a scale
Standard Deviation 22.07
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Core-30 (EORTC QLQ- C30) Score
C11D1: Nausea, vomiting
|
5.56 units on a scale
Standard Deviation 11.79
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Core-30 (EORTC QLQ- C30) Score
C11D1: Pain
|
12.96 units on a scale
Standard Deviation 18.22
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Core-30 (EORTC QLQ- C30) Score
C11D1: Dyspnoea
|
22.22 units on a scale
Standard Deviation 33.33
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Core-30 (EORTC QLQ- C30) Score
C11D1: Insomnia
|
25.00 units on a scale
Standard Deviation 34.50
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Core-30 (EORTC QLQ- C30) Score
C11D1: Appetite loss
|
25.93 units on a scale
Standard Deviation 32.39
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Core-30 (EORTC QLQ- C30) Score
C11D1: Constipation
|
7.41 units on a scale
Standard Deviation 14.70
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Core-30 (EORTC QLQ- C30) Score
C11D1: Diarrhea
|
33.33 units on a scale
Standard Deviation 16.67
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Core-30 (EORTC QLQ- C30) Score
C11D1: Financial difficulties
|
7.41 units on a scale
Standard Deviation 14.70
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Core-30 (EORTC QLQ- C30) Score
C12D1: GHS
|
77.78 units on a scale
Standard Deviation 27.22
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Core-30 (EORTC QLQ- C30) Score
C12D1: Physical functioning
|
85.56 units on a scale
Standard Deviation 19.96
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Core-30 (EORTC QLQ- C30) Score
C12D1: Role functioning
|
91.67 units on a scale
Standard Deviation 20.41
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Core-30 (EORTC QLQ- C30) Score
C12D1: Dyspnoea
|
27.78 units on a scale
Standard Deviation 44.31
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Core-30 (EORTC QLQ- C30) Score
C12D1: Insomnia
|
33.33 units on a scale
Standard Deviation 42.16
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Core-30 (EORTC QLQ- C30) Score
C12D1: Appetite loss
|
22.22 units on a scale
Standard Deviation 40.37
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Core-30 (EORTC QLQ- C30) Score
C12D1: Constipation
|
0.00 units on a scale
Standard Deviation 0.00
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Core-30 (EORTC QLQ- C30) Score
C12D1: Diarrhea
|
22.22 units on a scale
Standard Deviation 17.21
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Core-30 (EORTC QLQ- C30) Score
C12D1: Financial difficulties
|
5.56 units on a scale
Standard Deviation 13.61
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Core-30 (EORTC QLQ- C30) Score
C13D1: GHS
|
66.67 units on a scale
Standard Deviation 33.33
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Core-30 (EORTC QLQ- C30) Score
C13D1: Physical functioning
|
86.67 units on a scale
Standard Deviation 12.17
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Core-30 (EORTC QLQ- C30) Score
C13D1: Role functioning
|
83.33 units on a scale
Standard Deviation 33.33
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Core-30 (EORTC QLQ- C30) Score
C13D1: Emotional Functioning
|
61.11 units on a scale
Standard Deviation 33.68
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Core-30 (EORTC QLQ- C30) Score
C13D1: Cognitive Functioning
|
55.56 units on a scale
Standard Deviation 38.49
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Core-30 (EORTC QLQ- C30) Score
C13D1: Social Functioning
|
77.78 units on a scale
Standard Deviation 38.49
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Core-30 (EORTC QLQ- C30) Score
C13D1: Fatigue
|
40.28 units on a scale
Standard Deviation 30.56
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Core-30 (EORTC QLQ- C30) Score
C13D1: Pain
|
25.00 units on a scale
Standard Deviation 28.87
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Core-30 (EORTC QLQ- C30) Score
C13D1: Dyspnoea
|
33.33 units on a scale
Standard Deviation 38.49
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Core-30 (EORTC QLQ- C30) Score
C13D1: Insomnia
|
50.00 units on a scale
Standard Deviation 43.03
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Core-30 (EORTC QLQ- C30) Score
C13D1: Appetite loss
|
41.67 units on a scale
Standard Deviation 50.00
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Core-30 (EORTC QLQ- C30) Score
C13D1: Constipation
|
16.67 units on a scale
Standard Deviation 19.25
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Core-30 (EORTC QLQ- C30) Score
C13D1: Diarrhea
|
11.11 units on a scale
Standard Deviation 19.25
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Core-30 (EORTC QLQ- C30) Score
C13D1: Financial difficulties
|
11.11 units on a scale
Standard Deviation 19.25
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Core-30 (EORTC QLQ- C30) Score
C14D1: GHS
|
79.17 units on a scale
Standard Deviation 5.89
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Core-30 (EORTC QLQ- C30) Score
C14D1: Emotional Functioning
|
100.00 units on a scale
Standard Deviation 0.00
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Core-30 (EORTC QLQ- C30) Score
C14D1: Cognitive Functioning
|
91.67 units on a scale
Standard Deviation 11.79
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Core-30 (EORTC QLQ- C30) Score
C14D1: Social Functioning
|
100.00 units on a scale
Standard Deviation 0.00
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Core-30 (EORTC QLQ- C30) Score
C14D1: Fatigue
|
16.67 units on a scale
Standard Deviation 7.86
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Core-30 (EORTC QLQ- C30) Score
C14D1: Nausea, vomiting
|
8.33 units on a scale
Standard Deviation 11.79
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Core-30 (EORTC QLQ- C30) Score
C14D1: Pain
|
0.00 units on a scale
Standard Deviation 0.00
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Core-30 (EORTC QLQ- C30) Score
C14D1: Dyspnoea
|
16.67 units on a scale
Standard Deviation 23.57
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Core-30 (EORTC QLQ- C30) Score
C14D1: Insomnia
|
0.00 units on a scale
Standard Deviation 0.00
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Core-30 (EORTC QLQ- C30) Score
C14D1: Appetite loss
|
0.00 units on a scale
Standard Deviation 0.00
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Core-30 (EORTC QLQ- C30) Score
C14D1: Constipation
|
16.67 units on a scale
Standard Deviation 23.57
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Core-30 (EORTC QLQ- C30) Score
C14D1: Diarrhea
|
33.33 units on a scale
Standard Deviation 0.00
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Core-30 (EORTC QLQ- C30) Score
C15D1: Emotional Functioning
|
95.83 units on a scale
Standard Deviation 5.89
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Core-30 (EORTC QLQ- C30) Score
C15D1: Cognitive Functioning
|
91.67 units on a scale
Standard Deviation 11.79
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Core-30 (EORTC QLQ- C30) Score
C15D1: Social Functioning
|
100.00 units on a scale
Standard Deviation 0.00
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Core-30 (EORTC QLQ- C30) Score
C15D1: Fatigue
|
5.56 units on a scale
Standard Deviation 7.86
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Core-30 (EORTC QLQ- C30) Score
C15D1: Nausea, vomiting
|
0.00 units on a scale
Standard Deviation 0.00
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Core-30 (EORTC QLQ- C30) Score
C15D1: Pain
|
0.00 units on a scale
Standard Deviation 0.00
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Core-30 (EORTC QLQ- C30) Score
C15D1: Dyspnoea
|
0.00 units on a scale
Standard Deviation 0.00
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Core-30 (EORTC QLQ- C30) Score
C15D1: Constipation
|
16.67 units on a scale
Standard Deviation 23.57
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Core-30 (EORTC QLQ- C30) Score
C15D1: Diarrhea
|
33.33 units on a scale
Standard Deviation 0.00
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Core-30 (EORTC QLQ- C30) Score
C15D1: Financial difficulties
|
0.00 units on a scale
Standard Deviation 0.00
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Core-30 (EORTC QLQ- C30) Score
C16D1: GHS
|
87.50 units on a scale
Standard Deviation 5.89
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Core-30 (EORTC QLQ- C30) Score
C16D1: Physical functioning
|
96.67 units on a scale
Standard Deviation 4.71
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Core-30 (EORTC QLQ- C30) Score
C16D1: Role functioning
|
100.00 units on a scale
Standard Deviation 0.00
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Core-30 (EORTC QLQ- C30) Score
C16D1: Emotional Functioning
|
87.50 units on a scale
Standard Deviation 17.68
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Core-30 (EORTC QLQ- C30) Score
C16D1: Cognitive Functioning
|
91.67 units on a scale
Standard Deviation 11.79
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Core-30 (EORTC QLQ- C30) Score
C16D1: Social Functioning
|
100.00 units on a scale
Standard Deviation 0.00
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Core-30 (EORTC QLQ- C30) Score
C16D1: Fatigue
|
11.11 units on a scale
Standard Deviation 15.71
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Core-30 (EORTC QLQ- C30) Score
C16D1: Nausea, vomiting
|
0.00 units on a scale
Standard Deviation 0.00
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Core-30 (EORTC QLQ- C30) Score
C16D1: Pain
|
8.33 units on a scale
Standard Deviation 11.79
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Core-30 (EORTC QLQ- C30) Score
C16D1: Dyspnoea
|
0.00 units on a scale
Standard Deviation 0.00
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Core-30 (EORTC QLQ- C30) Score
C16D1: Insomnia
|
0.00 units on a scale
Standard Deviation 0.00
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Core-30 (EORTC QLQ- C30) Score
C16D1: Appetite loss
|
0.00 units on a scale
Standard Deviation 0.00
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Core-30 (EORTC QLQ- C30) Score
C16D1: Constipation
|
0.00 units on a scale
Standard Deviation 0.00
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Core-30 (EORTC QLQ- C30) Score
C16D1: Diarrhea
|
33.33 units on a scale
Standard Deviation 0.00
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Core-30 (EORTC QLQ- C30) Score
C16D1: Financial difficulties
|
0.00 units on a scale
Standard Deviation 0.00
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Core-30 (EORTC QLQ- C30) Score
C17D1: GHS
|
87.50 units on a scale
Standard Deviation 5.89
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Core-30 (EORTC QLQ- C30) Score
C17D1: Physical functioning
|
96.67 units on a scale
Standard Deviation 4.71
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Core-30 (EORTC QLQ- C30) Score
C17D1: Role functioning
|
100.00 units on a scale
Standard Deviation 0.00
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Core-30 (EORTC QLQ- C30) Score
C17D1: Emotional Functioning
|
87.50 units on a scale
Standard Deviation 17.68
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Core-30 (EORTC QLQ- C30) Score
C17D1: Cognitive Functioning
|
91.67 units on a scale
Standard Deviation 11.79
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Core-30 (EORTC QLQ- C30) Score
C17D1: Social Functioning
|
100.00 units on a scale
Standard Deviation 0.00
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Core-30 (EORTC QLQ- C30) Score
C17D1: Fatigue
|
11.11 units on a scale
Standard Deviation 15.71
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Core-30 (EORTC QLQ- C30) Score
C17D1: Nausea, vomiting
|
8.33 units on a scale
Standard Deviation 11.79
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Core-30 (EORTC QLQ- C30) Score
C17D1: Pain
|
0.00 units on a scale
Standard Deviation 0.00
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Core-30 (EORTC QLQ- C30) Score
C17D1: Dyspnoea
|
0.00 units on a scale
Standard Deviation 0.00
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Core-30 (EORTC QLQ- C30) Score
C17D1: Insomnia
|
16.67 units on a scale
Standard Deviation 23.57
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Core-30 (EORTC QLQ- C30) Score
C17D1: Appetite loss
|
16.67 units on a scale
Standard Deviation 23.57
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Core-30 (EORTC QLQ- C30) Score
C17D1: Constipation
|
0.00 units on a scale
Standard Deviation 0.00
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Core-30 (EORTC QLQ- C30) Score
C17D1: Diarrhea
|
33.33 units on a scale
Standard Deviation 0.00
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Core-30 (EORTC QLQ- C30) Score
C17D1: Financial difficulties
|
0.00 units on a scale
Standard Deviation 0.00
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Core-30 (EORTC QLQ- C30) Score
C18D1: GHS
|
79.17 units on a scale
Standard Deviation 5.89
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Core-30 (EORTC QLQ- C30) Score
C18D1: Physical functioning
|
96.67 units on a scale
Standard Deviation 4.71
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Core-30 (EORTC QLQ- C30) Score
C18D1: Role functioning
|
100.00 units on a scale
Standard Deviation 0.00
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Core-30 (EORTC QLQ- C30) Score
C18D1: Emotional Functioning
|
87.50 units on a scale
Standard Deviation 17.68
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Core-30 (EORTC QLQ- C30) Score
C18D1: Cognitive Functioning
|
100.00 units on a scale
Standard Deviation 0.00
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Core-30 (EORTC QLQ- C30) Score
C18D1: Social Functioning
|
100.00 units on a scale
Standard Deviation 0.00
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Core-30 (EORTC QLQ- C30) Score
C18D1: Fatigue
|
5.56 units on a scale
Standard Deviation 7.86
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Core-30 (EORTC QLQ- C30) Score
C18D1: Nausea, vomiting
|
8.33 units on a scale
Standard Deviation 11.79
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Core-30 (EORTC QLQ- C30) Score
C18D1: Pain
|
0.00 units on a scale
Standard Deviation 0.00
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Core-30 (EORTC QLQ- C30) Score
C18D1: Dyspnoea
|
0.00 units on a scale
Standard Deviation 0.00
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Core-30 (EORTC QLQ- C30) Score
C18D1: Insomnia
|
0.00 units on a scale
Standard Deviation 0.00
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Core-30 (EORTC QLQ- C30) Score
C18D1: Appetite loss
|
16.67 units on a scale
Standard Deviation 23.57
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Core-30 (EORTC QLQ- C30) Score
C18D1: Constipation
|
0.00 units on a scale
Standard Deviation 0.00
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Core-30 (EORTC QLQ- C30) Score
C18D1: Diarrhea
|
33.33 units on a scale
Standard Deviation 0.00
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Core-30 (EORTC QLQ- C30) Score
C18D1: Financial difficulties
|
0.00 units on a scale
Standard Deviation 0.00
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Core-30 (EORTC QLQ- C30) Score
C19D1: GHS
|
87.50 units on a scale
Standard Deviation 5.89
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Core-30 (EORTC QLQ- C30) Score
C19D1: Physical functioning
|
96.67 units on a scale
Standard Deviation 4.71
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Core-30 (EORTC QLQ- C30) Score
C19D1: Role functioning
|
100.00 units on a scale
Standard Deviation 0.00
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Core-30 (EORTC QLQ- C30) Score
C19D1: Emotional Functioning
|
95.83 units on a scale
Standard Deviation 5.89
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Core-30 (EORTC QLQ- C30) Score
C19D1: Nausea, vomiting
|
0.00 units on a scale
Standard Deviation 0.00
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Core-30 (EORTC QLQ- C30) Score
C19D1: Pain
|
16.67 units on a scale
Standard Deviation 0.00
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Core-30 (EORTC QLQ- C30) Score
C19D1: Dyspnoea
|
0.00 units on a scale
Standard Deviation 0.00
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Core-30 (EORTC QLQ- C30) Score
C19D1: Insomnia
|
33.33 units on a scale
Standard Deviation 0.00
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Core-30 (EORTC QLQ- C30) Score
C19D1: Appetite loss
|
0.00 units on a scale
Standard Deviation 0.00
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Core-30 (EORTC QLQ- C30) Score
C19D1: Constipation
|
0.00 units on a scale
Standard Deviation 0.00
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Core-30 (EORTC QLQ- C30) Score
C19D1: Diarrhea
|
50.00 units on a scale
Standard Deviation 23.57
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Core-30 (EORTC QLQ- C30) Score
C19D1: Financial difficulties
|
0.00 units on a scale
Standard Deviation 0.00
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Core-30 (EORTC QLQ- C30) Score
C20D1: GHS
|
83.33 units on a scale
Standard Deviation 0.00
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Core-30 (EORTC QLQ- C30) Score
C20D1: Physical functioning
|
100.00 units on a scale
Standard Deviation 0.00
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Core-30 (EORTC QLQ- C30) Score
C20D1: Social Functioning
|
100.00 units on a scale
Standard Deviation 0.00
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Core-30 (EORTC QLQ- C30) Score
C20D1: Fatigue
|
5.56 units on a scale
Standard Deviation 7.86
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Core-30 (EORTC QLQ- C30) Score
C20D1: Nausea, vomiting
|
0.00 units on a scale
Standard Deviation 0.00
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Core-30 (EORTC QLQ- C30) Score
C20D1: Pain
|
0.00 units on a scale
Standard Deviation 0.00
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Core-30 (EORTC QLQ- C30) Score
C20D1: Financial difficulties
|
0.00 units on a scale
Standard Deviation 0.00
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Core-30 (EORTC QLQ- C30) Score
C21D1: GHS
|
83.33 units on a scale
Standard Deviation 0.00
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Core-30 (EORTC QLQ- C30) Score
C21D1: Physical functioning
|
100.00 units on a scale
Standard Deviation 0.00
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Core-30 (EORTC QLQ- C30) Score
C21D1: Role functioning
|
100.00 units on a scale
Standard Deviation 0.00
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Core-30 (EORTC QLQ- C30) Score
C21D1: Emotional Functioning
|
91.67 units on a scale
Standard Deviation 11.79
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Core-30 (EORTC QLQ- C30) Score
C21D1: Cognitive Functioning
|
100.00 units on a scale
Standard Deviation 0.00
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Core-30 (EORTC QLQ- C30) Score
C21D1: Social Functioning
|
100.00 units on a scale
Standard Deviation 0.00
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Core-30 (EORTC QLQ- C30) Score
C21D1: Fatigue
|
5.56 units on a scale
Standard Deviation 7.86
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Core-30 (EORTC QLQ- C30) Score
C21D1: Nausea, vomiting
|
0.00 units on a scale
Standard Deviation 0.00
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Core-30 (EORTC QLQ- C30) Score
C21D1: Pain
|
0.00 units on a scale
Standard Deviation 0.00
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Core-30 (EORTC QLQ- C30) Score
C21D1: Dyspnoea
|
0.00 units on a scale
Standard Deviation 0.00
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Core-30 (EORTC QLQ- C30) Score
C21D1: Insomnia
|
0.00 units on a scale
Standard Deviation 0.00
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Core-30 (EORTC QLQ- C30) Score
C22D1: Role functioning
|
100.00 units on a scale
Standard Deviation 0.00
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Core-30 (EORTC QLQ- C30) Score
C22D1: Emotional Functioning
|
91.67 units on a scale
Standard Deviation 11.79
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Core-30 (EORTC QLQ- C30) Score
C22D1: Cognitive Functioning
|
100.00 units on a scale
Standard Deviation 0.00
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Core-30 (EORTC QLQ- C30) Score
C22D1: Social Functioning
|
100.00 units on a scale
Standard Deviation 0.00
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Core-30 (EORTC QLQ- C30) Score
C22D1: Fatigue
|
5.56 units on a scale
Standard Deviation 7.86
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Core-30 (EORTC QLQ- C30) Score
C22D1: Nausea, vomiting
|
0.00 units on a scale
Standard Deviation 0.00
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Core-30 (EORTC QLQ- C30) Score
C22D1: Pain
|
0.00 units on a scale
Standard Deviation 0.00
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Core-30 (EORTC QLQ- C30) Score
C22D1: Constipation
|
0.00 units on a scale
Standard Deviation 0.00
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Core-30 (EORTC QLQ- C30) Score
C22D1: Diarrhea
|
16.67 units on a scale
Standard Deviation 23.57
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Core-30 (EORTC QLQ- C30) Score
C22D1: Financial difficulties
|
0.00 units on a scale
Standard Deviation 0.00
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Core-30 (EORTC QLQ- C30) Score
C23D1: GHS
|
83.33 units on a scale
Standard Deviation 0.00
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Core-30 (EORTC QLQ- C30) Score
C23D1: Physical functioning
|
100.00 units on a scale
Standard Deviation 0.00
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Core-30 (EORTC QLQ- C30) Score
C23D1: Role functioning
|
100.00 units on a scale
Standard Deviation 0.00
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Core-30 (EORTC QLQ- C30) Score
C23D1: Emotional Functioning
|
87.50 units on a scale
Standard Deviation 17.68
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Core-30 (EORTC QLQ- C30) Score
C23D1: Cognitive Functioning
|
83.33 units on a scale
Standard Deviation 23.57
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Core-30 (EORTC QLQ- C30) Score
C23D1: Social Functioning
|
100.00 units on a scale
Standard Deviation 0.00
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Core-30 (EORTC QLQ- C30) Score
C23D1: Dyspnoea
|
0.00 units on a scale
Standard Deviation 0.00
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Core-30 (EORTC QLQ- C30) Score
C23D1: Insomnia
|
0.00 units on a scale
Standard Deviation 0.00
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Core-30 (EORTC QLQ- C30) Score
C23D1: Appetite loss
|
0.00 units on a scale
Standard Deviation 0.00
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Core-30 (EORTC QLQ- C30) Score
C23D1: Constipation
|
0.00 units on a scale
Standard Deviation 0.00
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Core-30 (EORTC QLQ- C30) Score
C23D1: Diarrhea
|
33.33 units on a scale
Standard Deviation 0.00
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Core-30 (EORTC QLQ- C30) Score
C23D1: Financial difficulties
|
0.00 units on a scale
Standard Deviation 0.00
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Core-30 (EORTC QLQ- C30) Score
C24D1: GHS
|
83.33 units on a scale
Standard Deviation 0.00
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Core-30 (EORTC QLQ- C30) Score
C24D1: Physical functioning
|
100.00 units on a scale
Standard Deviation 0.00
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Core-30 (EORTC QLQ- C30) Score
C24D1: Role functioning
|
100.00 units on a scale
Standard Deviation 0.00
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Core-30 (EORTC QLQ- C30) Score
C24D1: Emotional Functioning
|
83.33 units on a scale
Standard Deviation 23.57
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Core-30 (EORTC QLQ- C30) Score
C24D1: Cognitive Functioning
|
83.33 units on a scale
Standard Deviation 23.57
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Core-30 (EORTC QLQ- C30) Score
C24D1: Dyspnoea
|
0.00 units on a scale
Standard Deviation 0.00
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Core-30 (EORTC QLQ- C30) Score
C24D1: Insomnia
|
16.67 units on a scale
Standard Deviation 23.57
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Core-30 (EORTC QLQ- C30) Score
C24D1: Appetite loss
|
0.00 units on a scale
Standard Deviation 0.00
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Core-30 (EORTC QLQ- C30) Score
C24D1: Constipation
|
0.00 units on a scale
Standard Deviation 0.00
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Core-30 (EORTC QLQ- C30) Score
C24D1: Diarrhea
|
50.00 units on a scale
Standard Deviation 23.57
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Core-30 (EORTC QLQ- C30) Score
C25D1: Role functioning
|
100.00 units on a scale
Standard Deviation 0.00
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Core-30 (EORTC QLQ- C30) Score
C25D1: Emotional Functioning
|
95.83 units on a scale
Standard Deviation 5.89
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Core-30 (EORTC QLQ- C30) Score
C25D1: Cognitive Functioning
|
91.67 units on a scale
Standard Deviation 11.79
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Core-30 (EORTC QLQ- C30) Score
C25D1: Social Functioning
|
100.00 units on a scale
Standard Deviation 0.00
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Core-30 (EORTC QLQ- C30) Score
C26D1: Pain
|
0.00 units on a scale
Standard Deviation NA
Standard deviation was not estimable since only one participant was evaluable.
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Core-30 (EORTC QLQ- C30) Score
C26D1: Dyspnoea
|
0.00 units on a scale
Standard Deviation NA
Standard deviation was not estimable since only one participant was evaluable.
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Core-30 (EORTC QLQ- C30) Score
C26D1: Insomnia
|
0.00 units on a scale
Standard Deviation NA
Standard deviation was not estimable since only one participant was evaluable.
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Core-30 (EORTC QLQ- C30) Score
C27D1: Fatigue
|
0.00 units on a scale
Standard Deviation NA
Standard deviation was not estimable since only one participant was evaluable.
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Core-30 (EORTC QLQ- C30) Score
C27D1: Nausea, vomiting
|
0.00 units on a scale
Standard Deviation NA
Standard deviation was not estimable since only one participant was evaluable.
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Core-30 (EORTC QLQ- C30) Score
C27D1: Pain
|
0.00 units on a scale
Standard Deviation NA
Standard deviation was not estimable since only one participant was evaluable.
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Core-30 (EORTC QLQ- C30) Score
C27D1: Appetite loss
|
0.00 units on a scale
Standard Deviation NA
Standard deviation was not estimable since only one participant was evaluable.
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Core-30 (EORTC QLQ- C30) Score
C27D1: Constipation
|
0.00 units on a scale
Standard Deviation NA
Standard deviation was not estimable since only one participant was evaluable.
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Core-30 (EORTC QLQ- C30) Score
C27D1: Diarrhea
|
0.00 units on a scale
Standard Deviation NA
Standard deviation was not estimable since only one participant was evaluable.
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Core-30 (EORTC QLQ- C30) Score
C27D1: Financial difficulties
|
0.00 units on a scale
Standard Deviation NA
Standard deviation was not estimable since only one participant was evaluable.
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Core-30 (EORTC QLQ- C30) Score
C29D1: Fatigue
|
0.00 units on a scale
Standard Deviation NA
Standard deviation was not estimable since only one participant was evaluable.
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Core-30 (EORTC QLQ- C30) Score
C29D1: Nausea, vomiting
|
0.00 units on a scale
Standard Deviation NA
Standard deviation was not estimable since only one participant was evaluable.
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Core-30 (EORTC QLQ- C30) Score
C29D1: Pain
|
0.00 units on a scale
Standard Deviation NA
Standard deviation was not estimable since only one participant was evaluable.
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Core-30 (EORTC QLQ- C30) Score
C29D1: Dyspnoea
|
0.00 units on a scale
Standard Deviation NA
Standard deviation was not estimable since only one participant was evaluable.
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Core-30 (EORTC QLQ- C30) Score
C29D1: Insomnia
|
0.00 units on a scale
Standard Deviation NA
Standard deviation was not estimable since only one participant was evaluable.
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Core-30 (EORTC QLQ- C30) Score
C29D1: Appetite loss
|
0.00 units on a scale
Standard Deviation NA
Standard deviation was not estimable since only one participant was evaluable.
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Core-30 (EORTC QLQ- C30) Score
C29D1: Constipation
|
0.00 units on a scale
Standard Deviation NA
Standard deviation was not estimable since only one participant was evaluable.
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Core-30 (EORTC QLQ- C30) Score
C29D1: Diarrhea
|
33.33 units on a scale
Standard Deviation NA
Standard deviation was not estimable since only one participant was evaluable.
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Core-30 (EORTC QLQ- C30) Score
C29D1: Financial difficulties
|
0.00 units on a scale
Standard Deviation NA
Standard deviation was not estimable since only one participant was evaluable.
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Core-30 (EORTC QLQ- C30) Score
C30D1: GHS
|
83.33 units on a scale
Standard Deviation NA
Standard deviation was not estimable since only one participant was evaluable.
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Core-30 (EORTC QLQ- C30) Score
C30D1: Physical functioning
|
100.00 units on a scale
Standard Deviation NA
Standard deviation was not estimable since only one participant was evaluable.
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Core-30 (EORTC QLQ- C30) Score
C30D1: Role functioning
|
100.00 units on a scale
Standard Deviation NA
Standard deviation was not estimable since only one participant was evaluable.
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Core-30 (EORTC QLQ- C30) Score
C30D1: Emotional Functioning
|
100.00 units on a scale
Standard Deviation NA
Standard deviation was not estimable since only one participant was evaluable.
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Core-30 (EORTC QLQ- C30) Score
C30D1: Cognitive Functioning
|
100.00 units on a scale
Standard Deviation NA
Standard deviation was not estimable since only one participant was evaluable.
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Core-30 (EORTC QLQ- C30) Score
C30D1: Social Functioning
|
100.00 units on a scale
Standard Deviation NA
Standard deviation was not estimable since only one participant was evaluable.
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Core-30 (EORTC QLQ- C30) Score
C30D1: Fatigue
|
0.00 units on a scale
Standard Deviation NA
Standard deviation was not estimable since only one participant was evaluable.
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Core-30 (EORTC QLQ- C30) Score
C30D1: Nausea, vomiting
|
0.00 units on a scale
Standard Deviation NA
Standard deviation was not estimable since only one participant was evaluable.
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Core-30 (EORTC QLQ- C30) Score
C30D1: Pain
|
0.00 units on a scale
Standard Deviation NA
Standard deviation was not estimable since only one participant was evaluable.
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Core-30 (EORTC QLQ- C30) Score
C30D1: Dyspnoea
|
0.00 units on a scale
Standard Deviation NA
Standard deviation was not estimable since only one participant was evaluable.
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Core-30 (EORTC QLQ- C30) Score
C30D1: Insomnia
|
0.00 units on a scale
Standard Deviation NA
Standard deviation was not estimable since only one participant was evaluable.
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Core-30 (EORTC QLQ- C30) Score
C30D1: Appetite loss
|
0.00 units on a scale
Standard Deviation NA
Standard deviation was not estimable since only one participant was evaluable.
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Core-30 (EORTC QLQ- C30) Score
C30D1: Constipation
|
0.00 units on a scale
Standard Deviation NA
Standard deviation was not estimable since only one participant was evaluable.
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Core-30 (EORTC QLQ- C30) Score
C30D1: Diarrhea
|
0.00 units on a scale
Standard Deviation NA
Standard deviation was not estimable since only one participant was evaluable.
|
—
|
SECONDARY outcome
Timeframe: Baseline (C1D1), C2D1 thereafter every subsequent cycle up to C43Population: As-enrolled population included all participants who were enrolled in the study. Here, 'N' signifies those participants who were evaluable for the measure and 'number analyzed' signifies participants evaluable at each time point for each arm respectively.
QLQ-LC13 consisted of 13 questions relating to disease symptoms specific to lung cancer and treatment side effects typical of treatment with chemotherapy and radiotherapy. The 13 questions comprised 1 multi-item scale for dyspnoea and 10 single-item symptoms and side effects (coughing, hemoptysis, sore mouth, dysphagia, peripheral neuropathy, alopecia, chest pain, arm pain, other pain, and medicine for pain). Recall period: past week; response range: not at all to very much. Scale score range: 0 to 100. Higher symptom score = greater degree of symptoms.
Outcome measures
| Measure |
PF-00299804 (Adenocarcinoma Histology)
n=50 Participants
Participants with adenocarcinoma histology received PF-00299804 tablet 45 milligram (mg) orally once daily in cycles of 21 days until unacceptable toxicity, tumor progression, death, withdrawal from the study or investigator's discretion.
|
PF-00299804 (Non-adenocarcinoma Histology)
n=15 Participants
Participants with non-adenocarcinoma histology received PF-00299804 tablet 45 mg orally once daily in cycles of 21 days until unacceptable toxicity, tumor progression, death, withdrawal from the study or investigator's discretion.
|
|---|---|---|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Lung Cancer-13 (QLQ- LC13) Score
C1D1: Dyspnoea
|
25.85 units on a scale
Standard Deviation 22.84
|
26.98 units on a scale
Standard Deviation 21.67
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Lung Cancer-13 (QLQ- LC13) Score
C1D1: Coughing
|
33.33 units on a scale
Standard Deviation 30.12
|
33.33 units on a scale
Standard Deviation 25.20
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Lung Cancer-13 (QLQ- LC13) Score
C1D1: Peripheral neuropathy
|
10.00 units on a scale
Standard Deviation 18.13
|
13.33 units on a scale
Standard Deviation 24.56
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Lung Cancer-13 (QLQ- LC13) Score
C1D1: Alopecia
|
8.16 units on a scale
Standard Deviation 25.94
|
22.22 units on a scale
Standard Deviation 37.09
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Lung Cancer-13 (QLQ- LC13) Score
C2D1: Sore mouth
|
36.36 units on a scale
Standard Deviation 32.00
|
27.78 units on a scale
Standard Deviation 23.92
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Lung Cancer-13 (QLQ- LC13) Score
C4D1: Dyspnoea
|
15.81 units on a scale
Standard Deviation 16.08
|
31.94 units on a scale
Standard Deviation 26.85
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Lung Cancer-13 (QLQ- LC13) Score
C9D1: Sore mouth
|
7.41 units on a scale
Standard Deviation 14.70
|
0.00 units on a scale
Standard Deviation 0.00
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Lung Cancer-13 (QLQ- LC13) Score
C9D1: Other pain
|
22.22 units on a scale
Standard Deviation 23.57
|
55.56 units on a scale
Standard Deviation 50.92
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Lung Cancer-13 (QLQ- LC13) Score
C10D1: Dysphagia
|
11.11 units on a scale
Standard Deviation 16.67
|
0.00 units on a scale
Standard Deviation NA
Standard deviation was not estimable since only one participant was evaluable.
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Lung Cancer-13 (QLQ- LC13) Score
C13D1: Peripheral neuropathy
|
16.67 units on a scale
Standard Deviation 33.33
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Lung Cancer-13 (QLQ- LC13) Score
C13D1: Alopecia
|
16.67 units on a scale
Standard Deviation 19.25
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Lung Cancer-13 (QLQ- LC13) Score
C13D1: Chest pain
|
33.33 units on a scale
Standard Deviation 38.49
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Lung Cancer-13 (QLQ- LC13) Score
C14D1: Dyspnoea
|
0.00 units on a scale
Standard Deviation 0.00
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Lung Cancer-13 (QLQ- LC13) Score
C14D1: Chest pain
|
0.00 units on a scale
Standard Deviation 0.00
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Lung Cancer-13 (QLQ- LC13) Score
C16D1: Hemoptysis
|
0.00 units on a scale
Standard Deviation 0.00
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Lung Cancer-13 (QLQ- LC13) Score
C19D1: Arm pain
|
0.00 units on a scale
Standard Deviation 0.00
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Lung Cancer-13 (QLQ- LC13) Score
C19D1: Other pain
|
0.00 units on a scale
Standard Deviation 0.00
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Lung Cancer-13 (QLQ- LC13) Score
C20D1: Chest pain
|
0.00 units on a scale
Standard Deviation 0.00
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Lung Cancer-13 (QLQ- LC13) Score
C21D1: Coughing
|
33.33 units on a scale
Standard Deviation 0.00
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Lung Cancer-13 (QLQ- LC13) Score
C22D1: Dyspnoea
|
0.00 units on a scale
Standard Deviation 0.00
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Lung Cancer-13 (QLQ- LC13) Score
C22D1: Coughing
|
33.33 units on a scale
Standard Deviation 0.00
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Lung Cancer-13 (QLQ- LC13) Score
C22D1: Sore mouth
|
0.00 units on a scale
Standard Deviation 0.00
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Lung Cancer-13 (QLQ- LC13) Score
C24D1: Dyspnoea
|
0.00 units on a scale
Standard Deviation 0.00
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Lung Cancer-13 (QLQ- LC13) Score
C24D1: Coughing
|
33.33 units on a scale
Standard Deviation 0.00
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Lung Cancer-13 (QLQ- LC13) Score
C24D1: Dysphagia
|
16.67 units on a scale
Standard Deviation 23.57
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Lung Cancer-13 (QLQ- LC13) Score
C24D1: Peripheral neuropathy
|
16.67 units on a scale
Standard Deviation 23.57
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Lung Cancer-13 (QLQ- LC13) Score
C24D1: Alopecia
|
0.00 units on a scale
Standard Deviation 0.00
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Lung Cancer-13 (QLQ- LC13) Score
C25D1: Dyspnoea
|
0.00 units on a scale
Standard Deviation 0.00
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Lung Cancer-13 (QLQ- LC13) Score
C27D1: Alopecia
|
0.00 units on a scale
Standard Deviation NA
Standard deviation was not estimable since only one participant was evaluable.
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Lung Cancer-13 (QLQ- LC13) Score
C27D1: Chest pain
|
0.00 units on a scale
Standard Deviation NA
Standard deviation was not estimable since only one participant was evaluable.
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Lung Cancer-13 (QLQ- LC13) Score
C27D1: Other pain
|
0.00 units on a scale
Standard Deviation NA
Standard deviation was not estimable since only one participant was evaluable.
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Lung Cancer-13 (QLQ- LC13) Score
C29D1: Dyspnoea
|
0.00 units on a scale
Standard Deviation NA
Standard deviation was not estimable since only one participant was evaluable.
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Lung Cancer-13 (QLQ- LC13) Score
C29D1: Coughing
|
33.33 units on a scale
Standard Deviation NA
Standard deviation was not estimable since only one participant was evaluable.
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Lung Cancer-13 (QLQ- LC13) Score
C29D1: Hemoptysis
|
0.00 units on a scale
Standard Deviation NA
Standard deviation was not estimable since only one participant was evaluable.
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Lung Cancer-13 (QLQ- LC13) Score
C30D1: Alopecia
|
0.00 units on a scale
Standard Deviation NA
Standard deviation was not estimable since only one participant was evaluable.
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Lung Cancer-13 (QLQ- LC13) Score
C32D1: Dyspnoea
|
0.00 units on a scale
Standard Deviation NA
Standard deviation was not estimable since only one participant was evaluable.
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Lung Cancer-13 (QLQ- LC13) Score
C32D1: Coughing
|
33.33 units on a scale
Standard Deviation NA
Standard deviation was not estimable since only one participant was evaluable.
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Lung Cancer-13 (QLQ- LC13) Score
C32D1: Hemoptysis
|
0.00 units on a scale
Standard Deviation NA
Standard deviation was not estimable since only one participant was evaluable.
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Lung Cancer-13 (QLQ- LC13) Score
C32D1: Sore mouth
|
0.00 units on a scale
Standard Deviation NA
Standard deviation was not estimable since only one participant was evaluable.
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Lung Cancer-13 (QLQ- LC13) Score
C33D1: Dysphagia
|
0.00 units on a scale
Standard Deviation NA
Standard deviation was not estimable since only one participant was evaluable.
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Lung Cancer-13 (QLQ- LC13) Score
C33D1: Peripheral neuropathy
|
0.00 units on a scale
Standard Deviation NA
Standard deviation was not estimable since only one participant was evaluable.
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Lung Cancer-13 (QLQ- LC13) Score
C33D1: Alopecia
|
0.00 units on a scale
Standard Deviation NA
Standard deviation was not estimable since only one participant was evaluable.
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Lung Cancer-13 (QLQ- LC13) Score
C33D1: Other pain
|
0.00 units on a scale
Standard Deviation NA
Standard deviation was not estimable since only one participant was evaluable.
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Lung Cancer-13 (QLQ- LC13) Score
C34D1: Arm pain
|
0.00 units on a scale
Standard Deviation NA
Standard deviation was not estimable since only one participant was evaluable.
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Lung Cancer-13 (QLQ- LC13) Score
C34D1: Other pain
|
0.00 units on a scale
Standard Deviation NA
Standard deviation was not estimable since only one participant was evaluable.
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Lung Cancer-13 (QLQ- LC13) Score
C35D1: Sore mouth
|
0.00 units on a scale
Standard Deviation NA
Standard deviation was not estimable since only one participant was evaluable.
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Lung Cancer-13 (QLQ- LC13) Score
C35D1: Dysphagia
|
0.00 units on a scale
Standard Deviation NA
Standard deviation was not estimable since only one participant was evaluable.
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Lung Cancer-13 (QLQ- LC13) Score
C35D1: Other pain
|
0.00 units on a scale
Standard Deviation NA
Standard deviation was not estimable since only one participant was evaluable
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Lung Cancer-13 (QLQ- LC13) Score
C36D1: Hemoptysis
|
0.00 units on a scale
Standard Deviation NA
Standard deviation was not estimable since only one participant was evaluable.
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Lung Cancer-13 (QLQ- LC13) Score
C36D1: Sore mouth
|
0.00 units on a scale
Standard Deviation NA
Standard deviation was not estimable since only one participant was evaluable.
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Lung Cancer-13 (QLQ- LC13) Score
C36D1: Chest pain
|
0.00 units on a scale
Standard Deviation NA
Standard deviation was not estimable since only one participant was evaluable.
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Lung Cancer-13 (QLQ- LC13) Score
C36D1: Arm pain
|
0.00 units on a scale
Standard Deviation NA
Standard deviation was not estimable since only one participant was evaluable.
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Lung Cancer-13 (QLQ- LC13) Score
C38D1: Hemoptysis
|
0.00 units on a scale
Standard Deviation NA
Standard deviation was not estimable since only one participant was evaluable.
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Lung Cancer-13 (QLQ- LC13) Score
C38D1: Chest pain
|
0.00 units on a scale
Standard Deviation NA
Standard deviation was not estimable since only one participant was evaluable.
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Lung Cancer-13 (QLQ- LC13) Score
C39D1: Peripheral neuropathy
|
0.00 units on a scale
Standard Deviation NA
Standard deviation was not estimable since only one participant was evaluable.
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Lung Cancer-13 (QLQ- LC13) Score
C41D1: Other pain
|
0.00 units on a scale
Standard Deviation NA
Standard deviation was not estimable since only one participant was evaluable.
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Lung Cancer-13 (QLQ- LC13) Score
C21D1: Other pain
|
0.00 units on a scale
Standard Deviation 0.00
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Lung Cancer-13 (QLQ- LC13) Score
C22D1: Hemoptysis
|
0.00 units on a scale
Standard Deviation 0.00
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Lung Cancer-13 (QLQ- LC13) Score
C1D1: Hemoptysis
|
2.00 units on a scale
Standard Deviation 10.45
|
4.44 units on a scale
Standard Deviation 11.73
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Lung Cancer-13 (QLQ- LC13) Score
C1D1: Sore mouth
|
3.33 units on a scale
Standard Deviation 10.10
|
6.67 units on a scale
Standard Deviation 18.69
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Lung Cancer-13 (QLQ- LC13) Score
C1D1: Dysphagia
|
2.67 units on a scale
Standard Deviation 9.13
|
0.00 units on a scale
Standard Deviation 0.00
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Lung Cancer-13 (QLQ- LC13) Score
C1D1: Chest pain
|
14.67 units on a scale
Standard Deviation 27.07
|
20.00 units on a scale
Standard Deviation 30.34
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Lung Cancer-13 (QLQ- LC13) Score
C1D1: Arm pain
|
20.00 units on a scale
Standard Deviation 30.12
|
17.78 units on a scale
Standard Deviation 33.01
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Lung Cancer-13 (QLQ- LC13) Score
C1D1: Other pain
|
32.00 units on a scale
Standard Deviation 32.96
|
37.78 units on a scale
Standard Deviation 33.01
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Lung Cancer-13 (QLQ- LC13) Score
C2D1: Dyspnoea
|
18.69 units on a scale
Standard Deviation 20.02
|
26.85 units on a scale
Standard Deviation 23.43
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Lung Cancer-13 (QLQ- LC13) Score
C2D1: Coughing
|
19.70 units on a scale
Standard Deviation 19.45
|
33.33 units on a scale
Standard Deviation 24.62
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Lung Cancer-13 (QLQ- LC13) Score
C2D1: Hemoptysis
|
2.27 units on a scale
Standard Deviation 8.50
|
5.56 units on a scale
Standard Deviation 12.97
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Lung Cancer-13 (QLQ- LC13) Score
C2D1: Dysphagia
|
7.58 units on a scale
Standard Deviation 14.13
|
11.11 units on a scale
Standard Deviation 16.41
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Lung Cancer-13 (QLQ- LC13) Score
C2D1: Peripheral neuropathy
|
12.12 units on a scale
Standard Deviation 20.45
|
13.89 units on a scale
Standard Deviation 22.29
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Lung Cancer-13 (QLQ- LC13) Score
C2D1: Alopecia
|
6.06 units on a scale
Standard Deviation 20.68
|
8.33 units on a scale
Standard Deviation 15.08
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Lung Cancer-13 (QLQ- LC13) Score
C2D1: Chest pain
|
10.61 units on a scale
Standard Deviation 21.29
|
13.89 units on a scale
Standard Deviation 17.16
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Lung Cancer-13 (QLQ- LC13) Score
C2D1: Arm pain
|
14.39 units on a scale
Standard Deviation 20.83
|
19.44 units on a scale
Standard Deviation 38.82
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Lung Cancer-13 (QLQ- LC13) Score
C2D1: Other pain
|
22.76 units on a scale
Standard Deviation 26.29
|
16.67 units on a scale
Standard Deviation 30.15
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Lung Cancer-13 (QLQ- LC13) Score
C3D1: Dyspnoea
|
21.37 units on a scale
Standard Deviation 23.69
|
18.52 units on a scale
Standard Deviation 14.47
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Lung Cancer-13 (QLQ- LC13) Score
C3D1: Coughing
|
23.08 units on a scale
Standard Deviation 20.45
|
41.67 units on a scale
Standard Deviation 25.13
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Lung Cancer-13 (QLQ- LC13) Score
C3D1: Hemoptysis
|
1.67 units on a scale
Standard Deviation 7.36
|
5.56 units on a scale
Standard Deviation 12.97
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Lung Cancer-13 (QLQ- LC13) Score
C3D1: Sore mouth
|
30.00 units on a scale
Standard Deviation 31.85
|
16.67 units on a scale
Standard Deviation 22.47
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Lung Cancer-13 (QLQ- LC13) Score
C3D1: Dysphagia
|
11.67 units on a scale
Standard Deviation 24.52
|
11.11 units on a scale
Standard Deviation 21.71
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Lung Cancer-13 (QLQ- LC13) Score
C3D1: Peripheral neuropathy
|
16.24 units on a scale
Standard Deviation 24.03
|
22.22 units on a scale
Standard Deviation 25.95
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Lung Cancer-13 (QLQ- LC13) Score
C3D1: Alopecia
|
4.17 units on a scale
Standard Deviation 13.48
|
8.33 units on a scale
Standard Deviation 15.08
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Lung Cancer-13 (QLQ- LC13) Score
C3D1: Chest pain
|
11.67 units on a scale
Standard Deviation 23.33
|
19.44 units on a scale
Standard Deviation 22.29
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Lung Cancer-13 (QLQ- LC13) Score
C3D1: Arm pain
|
8.33 units on a scale
Standard Deviation 16.45
|
25.00 units on a scale
Standard Deviation 32.18
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Lung Cancer-13 (QLQ- LC13) Score
C3D1: Other pain
|
23.08 units on a scale
Standard Deviation 26.66
|
33.33 units on a scale
Standard Deviation 30.43
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Lung Cancer-13 (QLQ- LC13) Score
C4D1: Coughing
|
21.79 units on a scale
Standard Deviation 20.96
|
41.67 units on a scale
Standard Deviation 23.57
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Lung Cancer-13 (QLQ- LC13) Score
C4D1: Hemoptysis
|
2.56 units on a scale
Standard Deviation 9.06
|
4.17 units on a scale
Standard Deviation 11.79
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Lung Cancer-13 (QLQ- LC13) Score
C4D1: Sore mouth
|
19.23 units on a scale
Standard Deviation 19.26
|
20.83 units on a scale
Standard Deviation 24.80
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Lung Cancer-13 (QLQ- LC13) Score
C4D1: Dysphagia
|
7.69 units on a scale
Standard Deviation 14.32
|
16.67 units on a scale
Standard Deviation 30.86
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Lung Cancer-13 (QLQ- LC13) Score
C4D1: Peripheral neuropathy
|
19.23 units on a scale
Standard Deviation 28.55
|
25.00 units on a scale
Standard Deviation 15.43
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Lung Cancer-13 (QLQ- LC13) Score
C4D1: Alopecia
|
6.41 units on a scale
Standard Deviation 21.12
|
4.17 units on a scale
Standard Deviation 11.79
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Lung Cancer-13 (QLQ- LC13) Score
C4D1: Chest pain
|
3.85 units on a scale
Standard Deviation 10.86
|
20.83 units on a scale
Standard Deviation 30.54
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Lung Cancer-13 (QLQ- LC13) Score
C4D1: Arm pain
|
7.69 units on a scale
Standard Deviation 17.15
|
29.17 units on a scale
Standard Deviation 33.03
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Lung Cancer-13 (QLQ- LC13) Score
C4D1: Other pain
|
28.00 units on a scale
Standard Deviation 24.87
|
37.50 units on a scale
Standard Deviation 27.82
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Lung Cancer-13 (QLQ- LC13) Score
C5D1: Dyspnoea
|
20.51 units on a scale
Standard Deviation 17.12
|
20.63 units on a scale
Standard Deviation 13.50
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Lung Cancer-13 (QLQ- LC13) Score
C5D1: Coughing
|
25.64 units on a scale
Standard Deviation 17.15
|
42.86 units on a scale
Standard Deviation 16.27
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Lung Cancer-13 (QLQ- LC13) Score
C5D1: Hemoptysis
|
1.28 units on a scale
Standard Deviation 6.54
|
4.76 units on a scale
Standard Deviation 12.60
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Lung Cancer-13 (QLQ- LC13) Score
C5D1: Sore mouth
|
19.23 units on a scale
Standard Deviation 25.25
|
23.81 units on a scale
Standard Deviation 25.20
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Lung Cancer-13 (QLQ- LC13) Score
C5D1: Dysphagia
|
7.69 units on a scale
Standard Deviation 17.15
|
14.29 units on a scale
Standard Deviation 26.23
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Lung Cancer-13 (QLQ- LC13) Score
C5D1: Peripheral neuropathy
|
16.67 units on a scale
Standard Deviation 27.08
|
19.05 units on a scale
Standard Deviation 17.82
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Lung Cancer-13 (QLQ- LC13) Score
C5D1: Alopecia
|
8.97 units on a scale
Standard Deviation 22.23
|
9.52 units on a scale
Standard Deviation 16.27
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Lung Cancer-13 (QLQ- LC13) Score
C5D1: Chest pain
|
8.97 units on a scale
Standard Deviation 17.78
|
9.52 units on a scale
Standard Deviation 16.27
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Lung Cancer-13 (QLQ- LC13) Score
C5D1: Arm pain
|
10.26 units on a scale
Standard Deviation 22.65
|
23.81 units on a scale
Standard Deviation 37.09
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Lung Cancer-13 (QLQ- LC13) Score
C5D1: Other pain
|
21.33 units on a scale
Standard Deviation 30.25
|
33.33 units on a scale
Standard Deviation 38.49
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Lung Cancer-13 (QLQ- LC13) Score
C6D1: Dyspnoea
|
17.90 units on a scale
Standard Deviation 23.84
|
20.00 units on a scale
Standard Deviation 14.49
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Lung Cancer-13 (QLQ- LC13) Score
C6D1: Coughing
|
27.78 units on a scale
Standard Deviation 20.61
|
20.00 units on a scale
Standard Deviation 18.26
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Lung Cancer-13 (QLQ- LC13) Score
C6D1: Hemoptysis
|
3.70 units on a scale
Standard Deviation 10.78
|
0.00 units on a scale
Standard Deviation 0.00
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Lung Cancer-13 (QLQ- LC13) Score
C6D1: Sore mouth
|
22.22 units on a scale
Standard Deviation 22.87
|
26.67 units on a scale
Standard Deviation 27.89
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Lung Cancer-13 (QLQ- LC13) Score
C6D1: Dysphagia
|
3.70 units on a scale
Standard Deviation 10.78
|
0.00 units on a scale
Standard Deviation 0.00
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Lung Cancer-13 (QLQ- LC13) Score
C6D1: Peripheral neuropathy
|
16.67 units on a scale
Standard Deviation 23.57
|
46.67 units on a scale
Standard Deviation 38.01
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Lung Cancer-13 (QLQ- LC13) Score
C6D1: Alopecia
|
11.11 units on a scale
Standard Deviation 16.17
|
20.00 units on a scale
Standard Deviation 18.26
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Lung Cancer-13 (QLQ- LC13) Score
C6D1: Chest pain
|
7.41 units on a scale
Standard Deviation 18.28
|
0.00 units on a scale
Standard Deviation 0.00
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Lung Cancer-13 (QLQ- LC13) Score
C6D1: Arm pain
|
9.26 units on a scale
Standard Deviation 15.36
|
6.67 units on a scale
Standard Deviation 14.91
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Lung Cancer-13 (QLQ- LC13) Score
C6D1: Other pain
|
16.67 units on a scale
Standard Deviation 24.34
|
40.00 units on a scale
Standard Deviation 43.46
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Lung Cancer-13 (QLQ- LC13) Score
C7D1: Dyspnoea
|
17.46 units on a scale
Standard Deviation 18.85
|
19.44 units on a scale
Standard Deviation 16.67
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Lung Cancer-13 (QLQ- LC13) Score
C7D1: Coughing
|
21.43 units on a scale
Standard Deviation 21.11
|
16.67 units on a scale
Standard Deviation 19.25
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Lung Cancer-13 (QLQ- LC13) Score
C7D1: Hemoptysis
|
2.38 units on a scale
Standard Deviation 8.91
|
0.00 units on a scale
Standard Deviation 0.00
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Lung Cancer-13 (QLQ- LC13) Score
C7D1: Sore mouth
|
26.19 units on a scale
Standard Deviation 26.73
|
16.67 units on a scale
Standard Deviation 19.25
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Lung Cancer-13 (QLQ- LC13) Score
C7D1: Dysphagia
|
11.90 units on a scale
Standard Deviation 21.11
|
8.33 units on a scale
Standard Deviation 16.67
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Lung Cancer-13 (QLQ- LC13) Score
C7D1: Peripheral neuropathy
|
19.05 units on a scale
Standard Deviation 31.25
|
16.67 units on a scale
Standard Deviation 19.25
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Lung Cancer-13 (QLQ- LC13) Score
C7D1: Alopecia
|
11.90 units on a scale
Standard Deviation 16.57
|
8.33 units on a scale
Standard Deviation 16.67
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Lung Cancer-13 (QLQ- LC13) Score
C7D1: Chest pain
|
4.76 units on a scale
Standard Deviation 12.10
|
8.33 units on a scale
Standard Deviation 16.67
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Lung Cancer-13 (QLQ- LC13) Score
C7D1: Arm pain
|
11.90 units on a scale
Standard Deviation 21.11
|
8.33 units on a scale
Standard Deviation 16.67
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Lung Cancer-13 (QLQ- LC13) Score
C7D1: Other pain
|
15.38 units on a scale
Standard Deviation 22.01
|
25.00 units on a scale
Standard Deviation 31.91
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Lung Cancer-13 (QLQ- LC13) Score
C8D1: Dyspnoea
|
15.38 units on a scale
Standard Deviation 14.01
|
29.63 units on a scale
Standard Deviation 27.96
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Lung Cancer-13 (QLQ- LC13) Score
C8D1: Coughing
|
28.21 units on a scale
Standard Deviation 26.69
|
11.11 units on a scale
Standard Deviation 19.25
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Lung Cancer-13 (QLQ- LC13) Score
C8D1: Hemoptysis
|
5.13 units on a scale
Standard Deviation 12.52
|
0.00 units on a scale
Standard Deviation 0.00
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Lung Cancer-13 (QLQ- LC13) Score
C8D1: Sore mouth
|
12.82 units on a scale
Standard Deviation 16.88
|
22.22 units on a scale
Standard Deviation 19.25
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Lung Cancer-13 (QLQ- LC13) Score
C8D1: Dysphagia
|
7.69 units on a scale
Standard Deviation 14.62
|
11.11 units on a scale
Standard Deviation 19.25
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Lung Cancer-13 (QLQ- LC13) Score
C8D1: Peripheral neuropathy
|
15.38 units on a scale
Standard Deviation 22.01
|
33.33 units on a scale
Standard Deviation 0.00
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Lung Cancer-13 (QLQ- LC13) Score
C8D1: Alopecia
|
12.82 units on a scale
Standard Deviation 16.88
|
22.22 units on a scale
Standard Deviation 19.25
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Lung Cancer-13 (QLQ- LC13) Score
C8D1: Chest pain
|
7.69 units on a scale
Standard Deviation 14.62
|
0.00 units on a scale
Standard Deviation 0.00
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Lung Cancer-13 (QLQ- LC13) Score
C8D1: Arm pain
|
8.33 units on a scale
Standard Deviation 15.08
|
11.11 units on a scale
Standard Deviation 19.25
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Lung Cancer-13 (QLQ- LC13) Score
C8D1: Other pain
|
23.08 units on a scale
Standard Deviation 21.01
|
22.22 units on a scale
Standard Deviation 38.49
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Lung Cancer-13 (QLQ- LC13) Score
C9D1: Dyspnoea
|
23.46 units on a scale
Standard Deviation 20.37
|
25.93 units on a scale
Standard Deviation 23.13
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Lung Cancer-13 (QLQ- LC13) Score
C9D1: Coughing
|
29.63 units on a scale
Standard Deviation 20.03
|
11.11 units on a scale
Standard Deviation 19.25
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Lung Cancer-13 (QLQ- LC13) Score
C9D1: Hemoptysis
|
3.70 units on a scale
Standard Deviation 11.11
|
0.00 units on a scale
Standard Deviation 0.00
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Lung Cancer-13 (QLQ- LC13) Score
C9D1: Dysphagia
|
11.11 units on a scale
Standard Deviation 16.67
|
0.00 units on a scale
Standard Deviation 0.00
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Lung Cancer-13 (QLQ- LC13) Score
C9D1: Peripheral neuropathy
|
11.11 units on a scale
Standard Deviation 16.67
|
44.44 units on a scale
Standard Deviation 19.25
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Lung Cancer-13 (QLQ- LC13) Score
C9D1: Alopecia
|
8.33 units on a scale
Standard Deviation 15.43
|
22.22 units on a scale
Standard Deviation 19.25
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Lung Cancer-13 (QLQ- LC13) Score
C9D1: Chest pain
|
7.41 units on a scale
Standard Deviation 14.70
|
0.00 units on a scale
Standard Deviation 0.00
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Lung Cancer-13 (QLQ- LC13) Score
C9D1: Arm pain
|
14.81 units on a scale
Standard Deviation 24.22
|
22.22 units on a scale
Standard Deviation 38.49
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Lung Cancer-13 (QLQ- LC13) Score
C10D1: Dyspnoea
|
23.46 units on a scale
Standard Deviation 25.73
|
44.44 units on a scale
Standard Deviation NA
Standard deviation was not estimable since only one participant was evaluable.
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Lung Cancer-13 (QLQ- LC13) Score
C10D1: Coughing
|
25.93 units on a scale
Standard Deviation 22.22
|
33.33 units on a scale
Standard Deviation NA
Standard deviation was not estimable since only one participant was evaluable.
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Lung Cancer-13 (QLQ- LC13) Score
C10D1: Hemoptysis
|
3.70 units on a scale
Standard Deviation 11.11
|
0.00 units on a scale
Standard Deviation NA
Standard deviation was not estimable since only one participant was evaluable.
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Lung Cancer-13 (QLQ- LC13) Score
C10D1: Sore mouth
|
11.11 units on a scale
Standard Deviation 23.57
|
33.33 units on a scale
Standard Deviation NA
Standard deviation was not estimable since only one participant was evaluable.
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Lung Cancer-13 (QLQ- LC13) Score
C10D1: Peripheral neuropathy
|
18.52 units on a scale
Standard Deviation 24.22
|
33.33 units on a scale
Standard Deviation NA
Standard deviation was not estimable since only one participant was evaluable.
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Lung Cancer-13 (QLQ- LC13) Score
C10D1: Alopecia
|
14.81 units on a scale
Standard Deviation 17.57
|
66.67 units on a scale
Standard Deviation NA
Standard deviation was not estimable since only one participant was evaluable.
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Lung Cancer-13 (QLQ- LC13) Score
C10D1: Chest pain
|
3.70 units on a scale
Standard Deviation 11.11
|
0.00 units on a scale
Standard Deviation NA
Standard deviation was not estimable since only one participant was evaluable.
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Lung Cancer-13 (QLQ- LC13) Score
C10D1: Arm pain
|
14.81 units on a scale
Standard Deviation 24.22
|
0.00 units on a scale
Standard Deviation NA
Standard deviation was not estimable since only one participant was evaluable.
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Lung Cancer-13 (QLQ- LC13) Score
C10D1: Other pain
|
22.22 units on a scale
Standard Deviation 28.87
|
100.00 units on a scale
Standard Deviation NA
Standard deviation was not estimable since only one participant was evaluable.
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Lung Cancer-13 (QLQ- LC13) Score
C11D1: Dyspnoea
|
23.46 units on a scale
Standard Deviation 28.02
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Lung Cancer-13 (QLQ- LC13) Score
C11D1: Coughing
|
25.93 units on a scale
Standard Deviation 22.22
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Lung Cancer-13 (QLQ- LC13) Score
C11D1: Hemoptysis
|
3.70 units on a scale
Standard Deviation 11.11
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Lung Cancer-13 (QLQ- LC13) Score
C11D1: Sore mouth
|
11.11 units on a scale
Standard Deviation 23.57
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Lung Cancer-13 (QLQ- LC13) Score
C11D1: Dysphagia
|
0.00 units on a scale
Standard Deviation 0.00
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Lung Cancer-13 (QLQ- LC13) Score
C11D1: Peripheral neuropathy
|
14.81 units on a scale
Standard Deviation 33.79
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Lung Cancer-13 (QLQ- LC13) Score
C11D1: Alopecia
|
11.11 units on a scale
Standard Deviation 16.67
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Lung Cancer-13 (QLQ- LC13) Score
C11D1: Chest pain
|
11.11 units on a scale
Standard Deviation 16.67
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Lung Cancer-13 (QLQ- LC13) Score
C11D1: Arm pain
|
14.81 units on a scale
Standard Deviation 24.22
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Lung Cancer-13 (QLQ- LC13) Score
C11D1: Other pain
|
12.50 units on a scale
Standard Deviation 24.80
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Lung Cancer-13 (QLQ- LC13) Score
C12D1: Dyspnoea
|
22.22 units on a scale
Standard Deviation 34.43
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Lung Cancer-13 (QLQ- LC13) Score
C12D1: Coughing
|
27.78 units on a scale
Standard Deviation 25.09
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Lung Cancer-13 (QLQ- LC13) Score
C12D1: Hemoptysis
|
5.56 units on a scale
Standard Deviation 13.61
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Lung Cancer-13 (QLQ- LC13) Score
C12D1: Sore mouth
|
5.56 units on a scale
Standard Deviation 13.61
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Lung Cancer-13 (QLQ- LC13) Score
C12D1: Dysphagia
|
0.00 units on a scale
Standard Deviation 0.00
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Lung Cancer-13 (QLQ- LC13) Score
C12D1: Peripheral neuropathy
|
5.56 units on a scale
Standard Deviation 13.61
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Lung Cancer-13 (QLQ- LC13) Score
C12D1: Alopecia
|
16.67 units on a scale
Standard Deviation 18.26
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Lung Cancer-13 (QLQ- LC13) Score
C12D1: Chest pain
|
22.22 units on a scale
Standard Deviation 34.43
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Lung Cancer-13 (QLQ- LC13) Score
C12D1: Arm pain
|
22.22 units on a scale
Standard Deviation 34.43
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Lung Cancer-13 (QLQ- LC13) Score
C12D1: Other pain
|
22.22 units on a scale
Standard Deviation 40.37
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Lung Cancer-13 (QLQ- LC13) Score
C13D1: Dyspnoea
|
27.78 units on a scale
Standard Deviation 32.08
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Lung Cancer-13 (QLQ- LC13) Score
C13D1: Coughing
|
41.67 units on a scale
Standard Deviation 16.67
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Lung Cancer-13 (QLQ- LC13) Score
C13D1: Hemoptysis
|
8.33 units on a scale
Standard Deviation 16.67
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Lung Cancer-13 (QLQ- LC13) Score
C13D1: Sore mouth
|
16.67 units on a scale
Standard Deviation 19.25
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Lung Cancer-13 (QLQ- LC13) Score
C13D1: Dysphagia
|
8.33 units on a scale
Standard Deviation 16.67
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Lung Cancer-13 (QLQ- LC13) Score
C13D1: Arm pain
|
33.33 units on a scale
Standard Deviation 38.49
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Lung Cancer-13 (QLQ- LC13) Score
C13D1: Other pain
|
33.33 units on a scale
Standard Deviation 38.46
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Lung Cancer-13 (QLQ- LC13) Score
C14D1: Coughing
|
33.33 units on a scale
Standard Deviation 0.00
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Lung Cancer-13 (QLQ- LC13) Score
C14D1: Hemoptysis
|
0.00 units on a scale
Standard Deviation 0.00
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Lung Cancer-13 (QLQ- LC13) Score
C14D1: Sore mouth
|
0.00 units on a scale
Standard Deviation 0.00
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Lung Cancer-13 (QLQ- LC13) Score
C14D1: Dysphagia
|
16.67 units on a scale
Standard Deviation 23.57
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Lung Cancer-13 (QLQ- LC13) Score
C14D1: Peripheral neuropathy
|
0.00 units on a scale
Standard Deviation 0.00
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Lung Cancer-13 (QLQ- LC13) Score
C14D1: Alopecia
|
0.00 units on a scale
Standard Deviation 0.00
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Lung Cancer-13 (QLQ- LC13) Score
C14D1: Arm pain
|
0.00 units on a scale
Standard Deviation 0.00
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Lung Cancer-13 (QLQ- LC13) Score
C14D1: Other pain
|
0.00 units on a scale
Standard Deviation 0.00
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Lung Cancer-13 (QLQ- LC13) Score
C15D1: Dyspnoea
|
0.00 units on a scale
Standard Deviation 0.00
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Lung Cancer-13 (QLQ- LC13) Score
C15D1: Coughing
|
33.33 units on a scale
Standard Deviation 0.00
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Lung Cancer-13 (QLQ- LC13) Score
C15D1: Hemoptysis
|
0.00 units on a scale
Standard Deviation 0.00
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Lung Cancer-13 (QLQ- LC13) Score
C15D1: Sore mouth
|
0.00 units on a scale
Standard Deviation 0.00
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Lung Cancer-13 (QLQ- LC13) Score
C15D1: Dysphagia
|
0.00 units on a scale
Standard Deviation 0.00
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Lung Cancer-13 (QLQ- LC13) Score
C15D1: Peripheral neuropathy
|
0.00 units on a scale
Standard Deviation 0.00
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Lung Cancer-13 (QLQ- LC13) Score
C15D1: Alopecia
|
0.00 units on a scale
Standard Deviation 0.00
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Lung Cancer-13 (QLQ- LC13) Score
C15D1: Chest pain
|
0.00 units on a scale
Standard Deviation 0.00
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Lung Cancer-13 (QLQ- LC13) Score
C15D1: Arm pain
|
0.00 units on a scale
Standard Deviation 0.00
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Lung Cancer-13 (QLQ- LC13) Score
C15D1: Other pain
|
0.00 units on a scale
Standard Deviation 0.00
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Lung Cancer-13 (QLQ- LC13) Score
C16D1: Dyspnoea
|
0.00 units on a scale
Standard Deviation 0.00
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Lung Cancer-13 (QLQ- LC13) Score
C16D1: Coughing
|
16.67 units on a scale
Standard Deviation 23.57
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Lung Cancer-13 (QLQ- LC13) Score
C16D1: Sore mouth
|
0.00 units on a scale
Standard Deviation 0.00
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Lung Cancer-13 (QLQ- LC13) Score
C16D1: Dysphagia
|
0.00 units on a scale
Standard Deviation 0.00
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Lung Cancer-13 (QLQ- LC13) Score
C16D1: Peripheral neuropathy
|
0.00 units on a scale
Standard Deviation 0.00
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Lung Cancer-13 (QLQ- LC13) Score
C16D1: Alopecia
|
0.00 units on a scale
Standard Deviation 0.00
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Lung Cancer-13 (QLQ- LC13) Score
C16D1: Chest pain
|
0.00 units on a scale
Standard Deviation 0.00
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Lung Cancer-13 (QLQ- LC13) Score
C16D1: Arm pain
|
0.00 units on a scale
Standard Deviation 0.00
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Lung Cancer-13 (QLQ- LC13) Score
C16D1: Other pain
|
16.67 units on a scale
Standard Deviation 23.57
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Lung Cancer-13 (QLQ- LC13) Score
C17D1: Dyspnoea
|
0.00 units on a scale
Standard Deviation 0.00
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Lung Cancer-13 (QLQ- LC13) Score
C17D1: Coughing
|
33.33 units on a scale
Standard Deviation 0.00
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Lung Cancer-13 (QLQ- LC13) Score
C17D1: Hemoptysis
|
0.00 units on a scale
Standard Deviation 0.00
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Lung Cancer-13 (QLQ- LC13) Score
C17D1: Sore mouth
|
0.00 units on a scale
Standard Deviation 0.00
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Lung Cancer-13 (QLQ- LC13) Score
C17D1: Dysphagia
|
16.67 units on a scale
Standard Deviation 23.57
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Lung Cancer-13 (QLQ- LC13) Score
C17D1: Peripheral neuropathy
|
0.00 units on a scale
Standard Deviation 0.00
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Lung Cancer-13 (QLQ- LC13) Score
C17D1: Alopecia
|
0.00 units on a scale
Standard Deviation 0.00
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Lung Cancer-13 (QLQ- LC13) Score
C17D1: Chest pain
|
0.00 units on a scale
Standard Deviation 0.00
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Lung Cancer-13 (QLQ- LC13) Score
C17D1: Arm pain
|
0.00 units on a scale
Standard Deviation 0.00
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Lung Cancer-13 (QLQ- LC13) Score
C17D1: Other pain
|
0.00 units on a scale
Standard Deviation 0.00
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Lung Cancer-13 (QLQ- LC13) Score
C18D1: Dyspnoea
|
0.00 units on a scale
Standard Deviation 0.00
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Lung Cancer-13 (QLQ- LC13) Score
C18D1: Coughing
|
50.00 units on a scale
Standard Deviation 23.57
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Lung Cancer-13 (QLQ- LC13) Score
C18D1: Hemoptysis
|
0.00 units on a scale
Standard Deviation 0.00
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Lung Cancer-13 (QLQ- LC13) Score
C18D1: Sore mouth
|
0.00 units on a scale
Standard Deviation 0.00
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Lung Cancer-13 (QLQ- LC13) Score
C18D1: Dysphagia
|
16.67 units on a scale
Standard Deviation 23.57
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Lung Cancer-13 (QLQ- LC13) Score
C18D1: Peripheral neuropathy
|
0.00 units on a scale
Standard Deviation 0.00
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Lung Cancer-13 (QLQ- LC13) Score
C18D1: Alopecia
|
0.00 units on a scale
Standard Deviation 0.00
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Lung Cancer-13 (QLQ- LC13) Score
C18D1: Chest pain
|
0.00 units on a scale
Standard Deviation 0.00
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Lung Cancer-13 (QLQ- LC13) Score
C18D1: Arm pain
|
0.00 units on a scale
Standard Deviation 0.00
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Lung Cancer-13 (QLQ- LC13) Score
C18D1: Other pain
|
0.00 units on a scale
Standard Deviation 0.00
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Lung Cancer-13 (QLQ- LC13) Score
C19D1: Dyspnoea
|
0.00 units on a scale
Standard Deviation 0.00
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Lung Cancer-13 (QLQ- LC13) Score
C19D1: Coughing
|
33.33 units on a scale
Standard Deviation 33.33
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Lung Cancer-13 (QLQ- LC13) Score
C19D1: Hemoptysis
|
0.00 units on a scale
Standard Deviation 0.00
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Lung Cancer-13 (QLQ- LC13) Score
C19D1: Sore mouth
|
0.00 units on a scale
Standard Deviation 0.00
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Lung Cancer-13 (QLQ- LC13) Score
C19D1: Dysphagia
|
16.67 units on a scale
Standard Deviation 23.57
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Lung Cancer-13 (QLQ- LC13) Score
C19D1: Peripheral neuropathy
|
0.00 units on a scale
Standard Deviation 0.00
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Lung Cancer-13 (QLQ- LC13) Score
C19D1: Alopecia
|
0.00 units on a scale
Standard Deviation 0.00
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Lung Cancer-13 (QLQ- LC13) Score
C19D1: Chest pain
|
0.00 units on a scale
Standard Deviation 0.00
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Lung Cancer-13 (QLQ- LC13) Score
C20D1: Dyspnoea
|
0.00 units on a scale
Standard Deviation 0.00
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Lung Cancer-13 (QLQ- LC13) Score
C20D1: Coughing
|
33.33 units on a scale
Standard Deviation 0.00
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Lung Cancer-13 (QLQ- LC13) Score
C20D1: Hemoptysis
|
0.00 units on a scale
Standard Deviation 0.00
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Lung Cancer-13 (QLQ- LC13) Score
C20D1: Sore mouth
|
0.00 units on a scale
Standard Deviation 0.00
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Lung Cancer-13 (QLQ- LC13) Score
C20D1: Dysphagia
|
16.67 units on a scale
Standard Deviation 23.57
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Lung Cancer-13 (QLQ- LC13) Score
C20D1: Peripheral neuropathy
|
0.00 units on a scale
Standard Deviation 0.00
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Lung Cancer-13 (QLQ- LC13) Score
C20D1: Alopecia
|
0.00 units on a scale
Standard Deviation 0.00
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Lung Cancer-13 (QLQ- LC13) Score
C20D1: Arm pain
|
0.00 units on a scale
Standard Deviation 0.00
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Lung Cancer-13 (QLQ- LC13) Score
C20D1: Other pain
|
0.00 units on a scale
Standard Deviation 0.00
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Lung Cancer-13 (QLQ- LC13) Score
C21D1: Dyspnoea
|
0.00 units on a scale
Standard Deviation 0.00
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Lung Cancer-13 (QLQ- LC13) Score
C21D1: Hemoptysis
|
0.00 units on a scale
Standard Deviation 0.00
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Lung Cancer-13 (QLQ- LC13) Score
C21D1: Sore mouth
|
0.00 units on a scale
Standard Deviation 0.00
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Lung Cancer-13 (QLQ- LC13) Score
C21D1: Dysphagia
|
0.00 units on a scale
Standard Deviation 0.00
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Lung Cancer-13 (QLQ- LC13) Score
C21D1: Peripheral neuropathy
|
0.00 units on a scale
Standard Deviation 0.00
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Lung Cancer-13 (QLQ- LC13) Score
C21D1: Alopecia
|
0.00 units on a scale
Standard Deviation 0.00
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Lung Cancer-13 (QLQ- LC13) Score
C21D1: Chest pain
|
0.00 units on a scale
Standard Deviation 0.00
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Lung Cancer-13 (QLQ- LC13) Score
C21D1: Arm pain
|
0.00 units on a scale
Standard Deviation 0.00
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Lung Cancer-13 (QLQ- LC13) Score
C22D1: Dysphagia
|
0.00 units on a scale
Standard Deviation 0.00
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Lung Cancer-13 (QLQ- LC13) Score
C22D1: Peripheral neuropathy
|
0.00 units on a scale
Standard Deviation 0.00
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Lung Cancer-13 (QLQ- LC13) Score
C22D1: Alopecia
|
0.00 units on a scale
Standard Deviation 0.00
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Lung Cancer-13 (QLQ- LC13) Score
C22D1: Chest pain
|
0.00 units on a scale
Standard Deviation 0.00
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Lung Cancer-13 (QLQ- LC13) Score
C22D1: Arm pain
|
0.00 units on a scale
Standard Deviation 0.00
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Lung Cancer-13 (QLQ- LC13) Score
C39D1: Dysphagia
|
0.00 units on a scale
Standard Deviation NA
Standard deviation was not estimable since only one participant was evaluable.
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Lung Cancer-13 (QLQ- LC13) Score
C22D1: Other pain
|
0.00 units on a scale
Standard Deviation 0.00
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Lung Cancer-13 (QLQ- LC13) Score
C23D1: Dyspnoea
|
0.00 units on a scale
Standard Deviation 0.00
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Lung Cancer-13 (QLQ- LC13) Score
C23D1: Coughing
|
33.33 units on a scale
Standard Deviation 0.00
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Lung Cancer-13 (QLQ- LC13) Score
C23D1: Hemoptysis
|
0.00 units on a scale
Standard Deviation 0.00
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Lung Cancer-13 (QLQ- LC13) Score
C23D1: Sore mouth
|
0.00 units on a scale
Standard Deviation 0.00
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Lung Cancer-13 (QLQ- LC13) Score
C23D1: Dysphagia
|
0.00 units on a scale
Standard Deviation 0.00
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Lung Cancer-13 (QLQ- LC13) Score
C23D1: Peripheral neuropathy
|
0.00 units on a scale
Standard Deviation 0.00
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Lung Cancer-13 (QLQ- LC13) Score
C23D1: Alopecia
|
0.00 units on a scale
Standard Deviation 0.00
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Lung Cancer-13 (QLQ- LC13) Score
C23D1: Chest pain
|
0.00 units on a scale
Standard Deviation 0.00
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Lung Cancer-13 (QLQ- LC13) Score
C23D1: Arm pain
|
0.00 units on a scale
Standard Deviation 0.00
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Lung Cancer-13 (QLQ- LC13) Score
C23D1: Other pain
|
0.00 units on a scale
Standard Deviation 0.00
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Lung Cancer-13 (QLQ- LC13) Score
C24D1: Hemoptysis
|
0.00 units on a scale
Standard Deviation 0.00
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Lung Cancer-13 (QLQ- LC13) Score
C24D1: Sore mouth
|
0.00 units on a scale
Standard Deviation 0.00
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Lung Cancer-13 (QLQ- LC13) Score
C24D1: Chest pain
|
0.00 units on a scale
Standard Deviation 0.00
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Lung Cancer-13 (QLQ- LC13) Score
C24D1: Arm pain
|
0.00 units on a scale
Standard Deviation 0.00
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Lung Cancer-13 (QLQ- LC13) Score
C24D1: Other pain
|
16.67 units on a scale
Standard Deviation 23.57
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Lung Cancer-13 (QLQ- LC13) Score
C25D1: Coughing
|
33.33 units on a scale
Standard Deviation 0.00
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Lung Cancer-13 (QLQ- LC13) Score
C25D1: Hemoptysis
|
0.00 units on a scale
Standard Deviation 0.00
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Lung Cancer-13 (QLQ- LC13) Score
C25D1: Sore mouth
|
0.00 units on a scale
Standard Deviation 0.00
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Lung Cancer-13 (QLQ- LC13) Score
C25D1: Dysphagia
|
16.67 units on a scale
Standard Deviation 23.57
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Lung Cancer-13 (QLQ- LC13) Score
C25D1: Peripheral neuropathy
|
0.00 units on a scale
Standard Deviation 0.00
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Lung Cancer-13 (QLQ- LC13) Score
C25D1: Alopecia
|
16.67 units on a scale
Standard Deviation 23.57
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Lung Cancer-13 (QLQ- LC13) Score
C25D1: Chest pain
|
0.00 units on a scale
Standard Deviation 0.00
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Lung Cancer-13 (QLQ- LC13) Score
C25D1: Arm pain
|
0.00 units on a scale
Standard Deviation 0.00
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Lung Cancer-13 (QLQ- LC13) Score
C25D1: Other pain
|
0.00 units on a scale
Standard Deviation 0.00
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Lung Cancer-13 (QLQ- LC13) Score
C26D1: Dyspnoea
|
0.00 units on a scale
Standard Deviation NA
Standard deviation was not estimable since only one participant was evaluable
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Lung Cancer-13 (QLQ- LC13) Score
C26D1: Coughing
|
33.33 units on a scale
Standard Deviation NA
Standard deviation was not estimable since only one participant was evaluable
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Lung Cancer-13 (QLQ- LC13) Score
C26D1: Hemoptysis
|
0.00 units on a scale
Standard Deviation NA
Standard deviation was not estimable since only one participant was evaluable.
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Lung Cancer-13 (QLQ- LC13) Score
C26D1: Sore mouth
|
0.00 units on a scale
Standard Deviation NA
Standard deviation was not estimable since only one participant was evaluable.
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Lung Cancer-13 (QLQ- LC13) Score
C26D1: Dysphagia
|
0.00 units on a scale
Standard Deviation NA
Standard deviation was not estimable since only one participant was evaluable.
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Lung Cancer-13 (QLQ- LC13) Score
C26D1: Peripheral neuropathy
|
0.00 units on a scale
Standard Deviation NA
Standard deviation was not estimable since only one participant was evaluable.
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Lung Cancer-13 (QLQ- LC13) Score
C26D1: Alopecia
|
0.00 units on a scale
Standard Deviation NA
Standard deviation was not estimable since only one participant was evaluable.
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Lung Cancer-13 (QLQ- LC13) Score
C26D1: Chest pain
|
0.00 units on a scale
Standard Deviation NA
Standard deviation was not estimable since only one participant was evaluable.
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Lung Cancer-13 (QLQ- LC13) Score
C26D1: Arm pain
|
0.00 units on a scale
Standard Deviation NA
Standard deviation was not estimable since only one participant was evaluable.
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Lung Cancer-13 (QLQ- LC13) Score
C26D1: Other pain
|
0.00 units on a scale
Standard Deviation NA
Standard deviation was not estimable since only one participant was evaluable.
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Lung Cancer-13 (QLQ- LC13) Score
C27D1: Dyspnoea
|
0.00 units on a scale
Standard Deviation NA
Standard deviation was not estimable since only one participant was evaluable.
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Lung Cancer-13 (QLQ- LC13) Score
C27D1: Coughing
|
33.33 units on a scale
Standard Deviation NA
Standard deviation was not estimable since only one participant was evaluable.
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Lung Cancer-13 (QLQ- LC13) Score
C27D1: Hemoptysis
|
0.00 units on a scale
Standard Deviation NA
Standard deviation was not estimable since only one participant was evaluable.
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Lung Cancer-13 (QLQ- LC13) Score
C27D1: Sore mouth
|
0.00 units on a scale
Standard Deviation NA
Standard deviation was not estimable since only one participant was evaluable.
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Lung Cancer-13 (QLQ- LC13) Score
C27D1: Dysphagia
|
0.00 units on a scale
Standard Deviation NA
Standard deviation was not estimable since only one participant was evaluable.
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Lung Cancer-13 (QLQ- LC13) Score
C27D1: Peripheral neuropathy
|
0.00 units on a scale
Standard Deviation NA
Standard deviation was not estimable since only one participant was evaluable.
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Lung Cancer-13 (QLQ- LC13) Score
C27D1: Arm pain
|
0.00 units on a scale
Standard Deviation NA
Standard deviation was not estimable since only one participant was evaluable.
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Lung Cancer-13 (QLQ- LC13) Score
C29D1: Sore mouth
|
0.00 units on a scale
Standard Deviation NA
Standard deviation was not estimable since only one participant was evaluable.
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Lung Cancer-13 (QLQ- LC13) Score
C29D1: Dysphagia
|
0.00 units on a scale
Standard Deviation NA
Standard deviation was not estimable since only one participant was evaluable.
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Lung Cancer-13 (QLQ- LC13) Score
C29D1: Peripheral neuropathy
|
0.00 units on a scale
Standard Deviation NA
Standard deviation was not estimable since only one participant was evaluable.
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Lung Cancer-13 (QLQ- LC13) Score
C29D1: Alopecia
|
0.00 units on a scale
Standard Deviation NA
Standard deviation was not estimable since only one participant was evaluable.
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Lung Cancer-13 (QLQ- LC13) Score
C29D1: Chest pain
|
0.00 units on a scale
Standard Deviation 0.00
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Lung Cancer-13 (QLQ- LC13) Score
C29D1: Arm pain
|
0.00 units on a scale
Standard Deviation NA
Standard deviation was not estimable since only one participant was evaluable.
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Lung Cancer-13 (QLQ- LC13) Score
C29D1: Other pain
|
0.00 units on a scale
Standard Deviation NA
Standard deviation was not estimable since only one participant was evaluable.
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Lung Cancer-13 (QLQ- LC13) Score
C30D1: Dyspnoea
|
0.00 units on a scale
Standard Deviation NA
Standard deviation was not estimable since only one participant was evaluable.
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Lung Cancer-13 (QLQ- LC13) Score
C30D1: Coughing
|
0.00 units on a scale
Standard Deviation NA
Standard deviation was not estimable since only one participant was evaluable.
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Lung Cancer-13 (QLQ- LC13) Score
C30D1: Hemoptysis
|
0.00 units on a scale
Standard Deviation 0.00
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Lung Cancer-13 (QLQ- LC13) Score
C30D1: Sore mouth
|
0.00 units on a scale
Standard Deviation NA
Standard deviation was not estimable since only one participant was evaluable.
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Lung Cancer-13 (QLQ- LC13) Score
C30D1: Dysphagia
|
0.00 units on a scale
Standard Deviation NA
Standard deviation was not estimable since only one participant was evaluable.
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Lung Cancer-13 (QLQ- LC13) Score
C30D1: Peripheral neuropathy
|
0.00 units on a scale
Standard Deviation NA
Standard deviation was not estimable since only one participant was evaluable.
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Lung Cancer-13 (QLQ- LC13) Score
C30D1: Chest pain
|
0.00 units on a scale
Standard Deviation NA
Standard deviation was not estimable since only one participant was evaluable.
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Lung Cancer-13 (QLQ- LC13) Score
C30D1: Arm pain
|
0.00 units on a scale
Standard Deviation NA
Standard deviation was not estimable since only one participant was evaluable.
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Lung Cancer-13 (QLQ- LC13) Score
C30D1: Other pain
|
0.00 units on a scale
Standard Deviation NA
Standard deviation was not estimable since only one participant was evaluable.
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Lung Cancer-13 (QLQ- LC13) Score
C31D1: Dyspnoea
|
0.00 units on a scale
Standard Deviation NA
Standard deviation was not estimable since only one participant was evaluable.
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Lung Cancer-13 (QLQ- LC13) Score
C31D1: Coughing
|
33.33 units on a scale
Standard Deviation NA
Standard deviation was not estimable since only one participant was evaluable.
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Lung Cancer-13 (QLQ- LC13) Score
C31D1: Hemoptysis
|
0.00 units on a scale
Standard Deviation NA
Standard deviation was not estimable since only one participant was evaluable.
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Lung Cancer-13 (QLQ- LC13) Score
C31D1: Sore mouth
|
0.00 units on a scale
Standard Deviation NA
Standard deviation was not estimable since only one participant was evaluable.
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Lung Cancer-13 (QLQ- LC13) Score
C31D1: Dysphagia
|
0.00 units on a scale
Standard Deviation NA
Standard deviation was not estimable since only one participant was evaluable.
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Lung Cancer-13 (QLQ- LC13) Score
C31D1: Peripheral neuropathy
|
0.00 units on a scale
Standard Deviation NA
Standard deviation was not estimable since only one participant was evaluable.
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Lung Cancer-13 (QLQ- LC13) Score
C31D1: Alopecia
|
0.00 units on a scale
Standard Deviation NA
Standard deviation was not estimable since only one participant was evaluable.
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Lung Cancer-13 (QLQ- LC13) Score
C31D1: Chest pain
|
0.00 units on a scale
Standard Deviation NA
Standard deviation was not estimable since only one participant was evaluable.
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Lung Cancer-13 (QLQ- LC13) Score
C31D1: Arm pain
|
0.00 units on a scale
Standard Deviation NA
Standard deviation was not estimable since only one participant was evaluable.
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Lung Cancer-13 (QLQ- LC13) Score
C31D1: Other pain
|
0.00 units on a scale
Standard Deviation 0.00
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Lung Cancer-13 (QLQ- LC13) Score
C32D1: Dysphagia
|
0.00 units on a scale
Standard Deviation NA
Standard deviation was not estimable since only one participant was evaluable.
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Lung Cancer-13 (QLQ- LC13) Score
C32D1: Peripheral neuropathy
|
0.00 units on a scale
Standard Deviation NA
Standard deviation was not estimable since only one participant was evaluable.
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Lung Cancer-13 (QLQ- LC13) Score
C32D1: Alopecia
|
0.00 units on a scale
Standard Deviation NA
Standard deviation was not estimable since only one participant was evaluable.
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Lung Cancer-13 (QLQ- LC13) Score
C32D1: Chest pain
|
0.00 units on a scale
Standard Deviation NA
Standard deviation was not estimable since only one participant was evaluable.
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Lung Cancer-13 (QLQ- LC13) Score
C32D1: Arm pain
|
0.00 units on a scale
Standard Deviation NA
Standard deviation was not estimable since only one participant was evaluable.
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Lung Cancer-13 (QLQ- LC13) Score
C32D1: Other pain
|
0.00 units on a scale
Standard Deviation NA
Standard deviation was not estimable since only one participant was evaluable.
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Lung Cancer-13 (QLQ- LC13) Score
C33D1: Dyspnoea
|
0.00 units on a scale
Standard Deviation NA
Standard deviation was not estimable since only one participant was evaluable.
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Lung Cancer-13 (QLQ- LC13) Score
C33D1: Coughing
|
33.33 units on a scale
Standard Deviation NA
Standard deviation was not estimable since only one participant was evaluable.
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Lung Cancer-13 (QLQ- LC13) Score
C33D1: Hemoptysis
|
0.00 units on a scale
Standard Deviation NA
Standard deviation was not estimable since only one participant was evaluable.
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Lung Cancer-13 (QLQ- LC13) Score
C33D1: Sore mouth
|
0.00 units on a scale
Standard Deviation NA
Standard deviation was not estimable since only one participant was evaluable.
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Lung Cancer-13 (QLQ- LC13) Score
C33D1: Chest pain
|
0.00 units on a scale
Standard Deviation NA
Standard deviation was not estimable since only one participant was evaluable.
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Lung Cancer-13 (QLQ- LC13) Score
C33D1: Arm pain
|
0.00 units on a scale
Standard Deviation NA
Standard deviation was not estimable since only one participant was evaluable.
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Lung Cancer-13 (QLQ- LC13) Score
C34D1: Dyspnoea
|
0.00 units on a scale
Standard Deviation NA
Standard deviation was not estimable since only one participant was evaluable.
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Lung Cancer-13 (QLQ- LC13) Score
C34D1: Hemoptysis
|
0.00 units on a scale
Standard Deviation NA
Standard deviation was not estimable since only one participant was evaluable.
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Lung Cancer-13 (QLQ- LC13) Score
C34D1: Sore mouth
|
0.00 units on a scale
Standard Deviation NA
Standard deviation was not estimable since only one participant was evaluable.
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Lung Cancer-13 (QLQ- LC13) Score
C34D1: Dysphagia
|
0.00 units on a scale
Standard Deviation NA
Standard deviation was not estimable since only one participant was evaluable.
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Lung Cancer-13 (QLQ- LC13) Score
C34D1: Peripheral neuropathy
|
0.00 units on a scale
Standard Deviation NA
Standard deviation was not estimable since only one participant was evaluable.
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Lung Cancer-13 (QLQ- LC13) Score
C34D1: Alopecia
|
0.00 units on a scale
Standard Deviation NA
Standard deviation was not estimable since only one participant was evaluable.
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Lung Cancer-13 (QLQ- LC13) Score
C34D1: Chest pain
|
0.00 units on a scale
Standard Deviation NA
Standard deviation was not estimable since only one participant was evaluable.
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Lung Cancer-13 (QLQ- LC13) Score
C35D1: Dyspnoea
|
0.00 units on a scale
Standard Deviation NA
Standard deviation was not estimable since only one participant was evaluable.
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Lung Cancer-13 (QLQ- LC13) Score
C35D1: Coughing
|
33.33 units on a scale
Standard Deviation NA
Standard deviation was not estimable since only one participant was evaluable.
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Lung Cancer-13 (QLQ- LC13) Score
C35D1: Hemoptysis
|
0.00 units on a scale
Standard Deviation NA
Standard deviation was not estimable since only one participant was evaluable.
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Lung Cancer-13 (QLQ- LC13) Score
C35D1: Peripheral neuropathy
|
0.00 units on a scale
Standard Deviation NA
Standard deviation was not estimable since only one participant was evaluable.
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Lung Cancer-13 (QLQ- LC13) Score
C35D1: Alopecia
|
0.00 units on a scale
Standard Deviation NA
Standard deviation was not estimable since only one participant was evaluable.
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Lung Cancer-13 (QLQ- LC13) Score
C35D1: Chest pain
|
0.00 units on a scale
Standard Deviation NA
Standard deviation was not estimable since only one participant was evaluable.
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Lung Cancer-13 (QLQ- LC13) Score
C35D1: Arm pain
|
0.00 units on a scale
Standard Deviation NA
Standard deviation was not estimable since only one participant was evaluable.
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Lung Cancer-13 (QLQ- LC13) Score
C36D1: Dyspnoea
|
0.00 units on a scale
Standard Deviation NA
Standard deviation was not estimable since only one participant was evaluable.
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Lung Cancer-13 (QLQ- LC13) Score
C36D1: Coughing
|
33.33 units on a scale
Standard Deviation NA
Standard deviation was not estimable since only one participant was evaluable.
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Lung Cancer-13 (QLQ- LC13) Score
C36D1: Dysphagia
|
0.00 units on a scale
Standard Deviation NA
Standard deviation was not estimable since only one participant was evaluable.
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Lung Cancer-13 (QLQ- LC13) Score
C36D1: Peripheral neuropathy
|
0.00 units on a scale
Standard Deviation NA
Standard deviation was not estimable since only one participant was evaluable.
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Lung Cancer-13 (QLQ- LC13) Score
C36D1: Alopecia
|
0.00 units on a scale
Standard Deviation NA
Standard deviation was not estimable since only one participant was evaluable.
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Lung Cancer-13 (QLQ- LC13) Score
C36D1: Other pain
|
0.00 units on a scale
Standard Deviation NA
Standard deviation was not estimable since only one participant was evaluable.
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Lung Cancer-13 (QLQ- LC13) Score
C37D1: Dyspnoea
|
0.00 units on a scale
Standard Deviation NA
Standard deviation was not estimable since only one participant was evaluable.
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Lung Cancer-13 (QLQ- LC13) Score
C37D1: Coughing
|
33.33 units on a scale
Standard Deviation NA
Standard deviation was not estimable since only one participant was evaluable.
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Lung Cancer-13 (QLQ- LC13) Score
C37D1: Hemoptysis
|
0.00 units on a scale
Standard Deviation NA
Standard deviation was not estimable since only one participant was evaluable.
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Lung Cancer-13 (QLQ- LC13) Score
C37D1: Sore mouth
|
0.00 units on a scale
Standard Deviation NA
Standard deviation was not estimable since only one participant was evaluable.
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Lung Cancer-13 (QLQ- LC13) Score
C37D1: Dysphagia
|
0.00 units on a scale
Standard Deviation NA
Standard deviation was not estimable since only one participant was evaluable.
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Lung Cancer-13 (QLQ- LC13) Score
C37D1: Peripheral neuropathy
|
0.00 units on a scale
Standard Deviation NA
Standard deviation was not estimable since only one participant was evaluable.
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Lung Cancer-13 (QLQ- LC13) Score
C37D1: Alopecia
|
0.00 units on a scale
Standard Deviation NA
Standard deviation was not estimable since only one participant was evaluable.
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Lung Cancer-13 (QLQ- LC13) Score
C37D1: Chest pain
|
0.00 units on a scale
Standard Deviation NA
Standard deviation was not estimable since only one participant was evaluable.
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Lung Cancer-13 (QLQ- LC13) Score
C37D1: Arm pain
|
0.00 units on a scale
Standard Deviation NA
Standard deviation was not estimable since only one participant was evaluable.
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Lung Cancer-13 (QLQ- LC13) Score
C37D1: Other pain
|
0.00 units on a scale
Standard Deviation NA
Standard deviation was not estimable since only one participant was evaluable.
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Lung Cancer-13 (QLQ- LC13) Score
C38D1: Dyspnoea
|
0.00 units on a scale
Standard Deviation NA
Standard deviation was not estimable since only one participant was evaluable.
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Lung Cancer-13 (QLQ- LC13) Score
C38D1: Coughing
|
33.33 units on a scale
Standard Deviation NA
Standard deviation was not estimable since only one participant was evaluable.
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Lung Cancer-13 (QLQ- LC13) Score
C38D1: Sore mouth
|
0.00 units on a scale
Standard Deviation NA
Standard deviation was not estimable since only one participant was evaluable.
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Lung Cancer-13 (QLQ- LC13) Score
C38D1: Dysphagia
|
0.00 units on a scale
Standard Deviation NA
Standard deviation was not estimable since only one participant was evaluable.
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Lung Cancer-13 (QLQ- LC13) Score
C38D1: Peripheral neuropathy
|
0.00 units on a scale
Standard Deviation NA
Standard deviation was not estimable since only one participant was evaluable.
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Lung Cancer-13 (QLQ- LC13) Score
C38D1: Alopecia
|
0.00 units on a scale
Standard Deviation NA
Standard deviation was not estimable since only one participant was evaluable.
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Lung Cancer-13 (QLQ- LC13) Score
C38D1: Arm pain
|
0.00 units on a scale
Standard Deviation NA
Standard deviation was not estimable since only one participant was evaluable.
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Lung Cancer-13 (QLQ- LC13) Score
C38D1: Other pain
|
0.00 units on a scale
Standard Deviation NA
Standard deviation was not estimable since only one participant was evaluable.
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Lung Cancer-13 (QLQ- LC13) Score
C39D1: Dyspnoea
|
0.00 units on a scale
Standard Deviation NA
Standard deviation was not estimable since only one participant was evaluable.
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Lung Cancer-13 (QLQ- LC13) Score
C39D1: Coughing
|
0.00 units on a scale
Standard Deviation NA
Standard deviation was not estimable since only one participant was evaluable.
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Lung Cancer-13 (QLQ- LC13) Score
C39D1: Hemoptysis
|
0.00 units on a scale
Standard Deviation NA
Standard deviation was not estimable since only one participant was evaluable.
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Lung Cancer-13 (QLQ- LC13) Score
C39D1: Sore mouth
|
0.00 units on a scale
Standard Deviation NA
Standard deviation was not estimable since only one participant was evaluable.
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Lung Cancer-13 (QLQ- LC13) Score
C39D1: Alopecia
|
0.00 units on a scale
Standard Deviation NA
Standard deviation was not estimable since only one participant was evaluable.
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Lung Cancer-13 (QLQ- LC13) Score
C39D1: Chest pain
|
0.00 units on a scale
Standard Deviation NA
Standard deviation was not estimable since only one participant was evaluable.
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Lung Cancer-13 (QLQ- LC13) Score
C39D1: Arm pain
|
0.00 units on a scale
Standard Deviation NA
Standard deviation was not estimable since only one participant was evaluable.
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Lung Cancer-13 (QLQ- LC13) Score
C39D1: Other pain
|
0.00 units on a scale
Standard Deviation NA
Standard deviation was not estimable since only one participant was evaluable.
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Lung Cancer-13 (QLQ- LC13) Score
C40D1: Dyspnoea
|
0.00 units on a scale
Standard Deviation NA
Standard deviation was not estimable since only one participant was evaluable.
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Lung Cancer-13 (QLQ- LC13) Score
C40D1: Coughing
|
33.33 units on a scale
Standard Deviation NA
Standard deviation was not estimable since only one participant was evaluable.
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Lung Cancer-13 (QLQ- LC13) Score
C40D1: Hemoptysis
|
0.00 units on a scale
Standard Deviation NA
Standard deviation was not estimable since only one participant was evaluable.
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Lung Cancer-13 (QLQ- LC13) Score
C40D1: Sore mouth
|
0.00 units on a scale
Standard Deviation NA
Standard deviation was not estimable since only one participant was evaluable.
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Lung Cancer-13 (QLQ- LC13) Score
C40D1: Dysphagia
|
0.00 units on a scale
Standard Deviation NA
Standard deviation was not estimable since only one participant was evaluable.
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Lung Cancer-13 (QLQ- LC13) Score
C40D1: Peripheral neuropathy
|
0.00 units on a scale
Standard Deviation NA
Standard deviation was not estimable since only one participant was evaluable.
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Lung Cancer-13 (QLQ- LC13) Score
C40D1: Alopecia
|
0.00 units on a scale
Standard Deviation NA
Standard deviation was not estimable since only one participant was evaluable.
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Lung Cancer-13 (QLQ- LC13) Score
C40D1: Chest pain
|
0.00 units on a scale
Standard Deviation NA
Standard deviation was not estimable since only one participant was evaluable.
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Lung Cancer-13 (QLQ- LC13) Score
C40D1: Arm pain
|
0.00 units on a scale
Standard Deviation NA
Standard deviation was not estimable since only one participant was evaluable.
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Lung Cancer-13 (QLQ- LC13) Score
C40D1: Other pain
|
0.00 units on a scale
Standard Deviation NA
Standard deviation was not estimable since only one participant was evaluable.
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Lung Cancer-13 (QLQ- LC13) Score
C41D1: Dyspnoea
|
0.00 units on a scale
Standard Deviation NA
Standard deviation was not estimable since only one participant was evaluable.
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Lung Cancer-13 (QLQ- LC13) Score
C41D1: Hemoptysis
|
0.00 units on a scale
Standard Deviation NA
Standard deviation was not estimable since only one participant was evaluable.
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Lung Cancer-13 (QLQ- LC13) Score
C41D1: Sore mouth
|
0.00 units on a scale
Standard Deviation NA
Standard deviation was not estimable since only one participant was evaluable.
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Lung Cancer-13 (QLQ- LC13) Score
C41D1: Dysphagia
|
0.00 units on a scale
Standard Deviation NA
Standard deviation was not estimable since only one participant was evaluable.
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Lung Cancer-13 (QLQ- LC13) Score
C41D1: Peripheral neuropathy
|
0.00 units on a scale
Standard Deviation NA
Standard deviation was not estimable since only one participant was evaluable.
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Lung Cancer-13 (QLQ- LC13) Score
C41D1: Alopecia
|
0.00 units on a scale
Standard Deviation NA
Standard deviation was not estimable since only one participant was evaluable.
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Lung Cancer-13 (QLQ- LC13) Score
C41D1: Chest pain
|
0.00 units on a scale
Standard Deviation NA
Standard deviation was not estimable since only one participant was evaluable.
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Lung Cancer-13 (QLQ- LC13) Score
C41D1: Arm pain
|
0.00 units on a scale
Standard Deviation NA
Standard deviation was not estimable since only one participant was evaluable.
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Lung Cancer-13 (QLQ- LC13) Score
C42D1: Dyspnoea
|
0.00 units on a scale
Standard Deviation NA
Standard deviation was not estimable since only one participant was evaluable.
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Lung Cancer-13 (QLQ- LC13) Score
C42D1: Coughing
|
33.33 units on a scale
Standard Deviation NA
Standard deviation was not estimable since only one participant was evaluable.
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Lung Cancer-13 (QLQ- LC13) Score
C42D1: Peripheral neuropathy
|
0.00 units on a scale
Standard Deviation NA
Standard deviation was not estimable since only one participant was evaluable.
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Lung Cancer-13 (QLQ- LC13) Score
C43D1: Hemoptysis
|
0.00 units on a scale
Standard Deviation NA
Standard deviation was not estimable since only one participant was evaluable.
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Lung Cancer-13 (QLQ- LC13) Score
C43D1: Sore mouth
|
0.00 units on a scale
Standard Deviation 0.00
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Lung Cancer-13 (QLQ- LC13) Score
C42D1: Hemoptysis
|
0.00 units on a scale
Standard Deviation NA
Standard deviation was not estimable since only one participant was evaluable.
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Lung Cancer-13 (QLQ- LC13) Score
C42D1: Sore mouth
|
0.00 units on a scale
Standard Deviation NA
Standard deviation was not estimable since only one participant was evaluable.
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Lung Cancer-13 (QLQ- LC13) Score
C43D1: Dysphagia
|
0.00 units on a scale
Standard Deviation NA
Standard deviation was not estimable since only one participant was evaluable.
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Lung Cancer-13 (QLQ- LC13) Score
C42D1: Dysphagia
|
0.00 units on a scale
Standard Deviation NA
Standard deviation was not estimable since only one participant was evaluable.
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Lung Cancer-13 (QLQ- LC13) Score
C43D1: Peripheral neuropathy
|
0.00 units on a scale
Standard Deviation NA
Standard deviation was not estimable since only one participant was evaluable.
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Lung Cancer-13 (QLQ- LC13) Score
C43D1: Alopecia
|
0.00 units on a scale
Standard Deviation NA
Standard deviation was not estimable since only one participant was evaluable.
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Lung Cancer-13 (QLQ- LC13) Score
C43D1: Chest pain
|
0.00 units on a scale
Standard Deviation NA
Standard deviation was not estimable since only one participant was evaluable.
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Lung Cancer-13 (QLQ- LC13) Score
C43D1: Arm pain
|
0.00 units on a scale
Standard Deviation NA
Standard deviation was not estimable since only one participant was evaluable.
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Lung Cancer-13 (QLQ- LC13) Score
C43D1: Other pain
|
0.00 units on a scale
Standard Deviation NA
Standard deviation was not estimable since only one participant was evaluable.
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Lung Cancer-13 (QLQ- LC13) Score
C42D1: Alopecia
|
0.00 units on a scale
Standard Deviation NA
Standard deviation was not estimable since only one participant was evaluable.
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Lung Cancer-13 (QLQ- LC13) Score
C42D1: Chest pain
|
0.00 units on a scale
Standard Deviation NA
Standard deviation was not estimable since only one participant was evaluable.
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Lung Cancer-13 (QLQ- LC13) Score
C42D1: Arm pain
|
0.00 units on a scale
Standard Deviation NA
Standard deviation was not estimable since only one participant was evaluable.
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Lung Cancer-13 (QLQ- LC13) Score
C43D1: Dyspnoea
|
0.00 units on a scale
Standard Deviation NA
Standard deviation was not estimable since only one participant was evaluable.
|
—
|
|
European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Lung Cancer-13 (QLQ- LC13) Score
C43D1: Coughing
|
0.00 units on a scale
Standard Deviation NA
Standard deviation was not estimable since only one participant was evaluable.
|
—
|
SECONDARY outcome
Timeframe: Baseline (C1D1), C2D1 thereafter every subsequent cycle up to C43Population: As-enrolled population included all participants who were enrolled in the study. Here, 'N' signifies those participants who were evaluable for the measure and 'number analyzed' signifies participants evaluable at each time point for each arm respectively.
Self-administered questionnaire to measure health-related quality of life (QoL) of adult participants suffering from skin disease; 10 questions concerning participants' perception of impact of their disease over last week encompassing aspects such as symptoms or feelings, daily activities, leisure, work or school, personal relationships and treatment. Questions scored on a 4-point Likert scale: 0 (not relevant), 1 (a little), 2 (a lot), and 3 (very much). Scores of individual questions (0-3) were added to yield a total score (0-30); higher score = greater impairment of participant's QoL.
Outcome measures
| Measure |
PF-00299804 (Adenocarcinoma Histology)
n=50 Participants
Participants with adenocarcinoma histology received PF-00299804 tablet 45 milligram (mg) orally once daily in cycles of 21 days until unacceptable toxicity, tumor progression, death, withdrawal from the study or investigator's discretion.
|
PF-00299804 (Non-adenocarcinoma Histology)
n=15 Participants
Participants with non-adenocarcinoma histology received PF-00299804 tablet 45 mg orally once daily in cycles of 21 days until unacceptable toxicity, tumor progression, death, withdrawal from the study or investigator's discretion.
|
|---|---|---|
|
Dermatology Life Quality Index (DLQI) Score
C5D1
|
4.67 units on a scale
Standard Deviation 4.12
|
6.00 units on a scale
Standard Deviation 7.62
|
|
Dermatology Life Quality Index (DLQI) Score
C1D1
|
0.38 units on a scale
Standard Deviation 0.54
|
0.80 units on a scale
Standard Deviation 1.52
|
|
Dermatology Life Quality Index (DLQI) Score
C33D1
|
0.00 units on a scale
Standard Deviation NA
Standard deviation was not estimable since only one participant was evaluable.
|
—
|
|
Dermatology Life Quality Index (DLQI) Score
C39D1
|
0.00 units on a scale
Standard Deviation NA
Standard deviation was not estimable since only one participant was evaluable.
|
—
|
|
Dermatology Life Quality Index (DLQI) Score
C6D1
|
4.39 units on a scale
Standard Deviation 4.65
|
6.00 units on a scale
Standard Deviation 6.40
|
|
Dermatology Life Quality Index (DLQI) Score
C4D1
|
3.56 units on a scale
Standard Deviation 3.62
|
5.13 units on a scale
Standard Deviation 5.06
|
|
Dermatology Life Quality Index (DLQI) Score
C2D1
|
3.34 units on a scale
Standard Deviation 4.37
|
2.08 units on a scale
Standard Deviation 2.22
|
|
Dermatology Life Quality Index (DLQI) Score
C3D1
|
4.08 units on a scale
Standard Deviation 4.31
|
3.08 units on a scale
Standard Deviation 3.99
|
|
Dermatology Life Quality Index (DLQI) Score
C7D1
|
4.00 units on a scale
Standard Deviation 5.28
|
5.00 units on a scale
Standard Deviation 6.06
|
|
Dermatology Life Quality Index (DLQI) Score
C8D1
|
3.31 units on a scale
Standard Deviation 3.57
|
3.67 units on a scale
Standard Deviation 3.21
|
|
Dermatology Life Quality Index (DLQI) Score
C9D1
|
1.78 units on a scale
Standard Deviation 2.49
|
2.50 units on a scale
Standard Deviation 3.54
|
|
Dermatology Life Quality Index (DLQI) Score
C10D1
|
2.22 units on a scale
Standard Deviation 2.54
|
8.00 units on a scale
Standard Deviation NA
Standard deviation was not estimable since only one participant was evaluable.
|
|
Dermatology Life Quality Index (DLQI) Score
C11D1
|
2.78 units on a scale
Standard Deviation 3.35
|
—
|
|
Dermatology Life Quality Index (DLQI) Score
C12D1
|
2.00 units on a scale
Standard Deviation 3.95
|
—
|
|
Dermatology Life Quality Index (DLQI) Score
C13D1
|
4.00 units on a scale
Standard Deviation 3.65
|
—
|
|
Dermatology Life Quality Index (DLQI) Score
C14D1
|
1.50 units on a scale
Standard Deviation 0.71
|
—
|
|
Dermatology Life Quality Index (DLQI) Score
C15D1
|
1.00 units on a scale
Standard Deviation 1.41
|
—
|
|
Dermatology Life Quality Index (DLQI) Score
C16D1
|
2.00 units on a scale
Standard Deviation 0.00
|
—
|
|
Dermatology Life Quality Index (DLQI) Score
C17D1
|
0.50 units on a scale
Standard Deviation 0.71
|
—
|
|
Dermatology Life Quality Index (DLQI) Score
C18D1
|
0.50 units on a scale
Standard Deviation 0.71
|
—
|
|
Dermatology Life Quality Index (DLQI) Score
C19D1
|
1.00 units on a scale
Standard Deviation 1.41
|
—
|
|
Dermatology Life Quality Index (DLQI) Score
C20D1
|
0.50 units on a scale
Standard Deviation 0.71
|
—
|
|
Dermatology Life Quality Index (DLQI) Score
C21D1
|
1.00 units on a scale
Standard Deviation 1.41
|
—
|
|
Dermatology Life Quality Index (DLQI) Score
C22D1
|
1.00 units on a scale
Standard Deviation 1.41
|
—
|
|
Dermatology Life Quality Index (DLQI) Score
C23D1
|
8.00 units on a scale
Standard Deviation 11.31
|
—
|
|
Dermatology Life Quality Index (DLQI) Score
C24D1
|
1.00 units on a scale
Standard Deviation 1.41
|
—
|
|
Dermatology Life Quality Index (DLQI) Score
C25D1
|
3.00 units on a scale
Standard Deviation 0.00
|
—
|
|
Dermatology Life Quality Index (DLQI) Score
C26D1
|
2.00 units on a scale
Standard Deviation NA
Standard deviation was not estimable since only one participant was evaluable.
|
—
|
|
Dermatology Life Quality Index (DLQI) Score
C27D1
|
1.00 units on a scale
Standard Deviation NA
Standard deviation was not estimable since only one participant was evaluable.
|
—
|
|
Dermatology Life Quality Index (DLQI) Score
C29D1
|
0.00 units on a scale
Standard Deviation NA
Standard deviation was not estimable since only one participant was evaluable.
|
—
|
|
Dermatology Life Quality Index (DLQI) Score
C30D1
|
0.00 units on a scale
Standard Deviation NA
Standard deviation was not estimable since only one participant was evaluable.
|
—
|
|
Dermatology Life Quality Index (DLQI) Score
C31D1
|
0.00 units on a scale
Standard Deviation NA
Standard deviation was not estimable since only one participant was evaluable.
|
—
|
|
Dermatology Life Quality Index (DLQI) Score
C32D1
|
0.00 units on a scale
Standard Deviation NA
Standard deviation was not estimable since only one participant was evaluable.
|
—
|
|
Dermatology Life Quality Index (DLQI) Score
C34D1
|
0.00 units on a scale
Standard Deviation NA
Standard deviation was not estimable since only one participant was evaluable.
|
—
|
|
Dermatology Life Quality Index (DLQI) Score
C35D1
|
0.00 units on a scale
Standard Deviation NA
Standard deviation was not estimable since only one participant was evaluable.
|
—
|
|
Dermatology Life Quality Index (DLQI) Score
C36D1
|
0.00 units on a scale
Standard Deviation NA
Standard deviation was not estimable since only one participant was evaluable.
|
—
|
|
Dermatology Life Quality Index (DLQI) Score
C37D1
|
0.00 units on a scale
Standard Deviation NA
Standard deviation was not estimable since only one participant was evaluable.
|
—
|
|
Dermatology Life Quality Index (DLQI) Score
C38D1
|
0.00 units on a scale
Standard Deviation NA
Standard deviation was not estimable since only one participant was evaluable.
|
—
|
|
Dermatology Life Quality Index (DLQI) Score
C40D1
|
0.00 units on a scale
Standard Deviation NA
Standard deviation was not estimable since only one participant was evaluable.
|
—
|
|
Dermatology Life Quality Index (DLQI) Score
C41D1
|
0.00 units on a scale
Standard Deviation NA
Standard deviation was not estimable since only one participant was evaluable.
|
—
|
|
Dermatology Life Quality Index (DLQI) Score
C42D1
|
0.00 units on a scale
Standard Deviation NA
Standard deviation was not estimable since only one participant was evaluable.
|
—
|
|
Dermatology Life Quality Index (DLQI) Score
C43D1
|
0.00 units on a scale
Standard Deviation NA
Standard deviation was not estimable since only one participant was evaluable.
|
—
|
SECONDARY outcome
Timeframe: Month 6Population: As-enrolled population included all participants who were enrolled in the study.
PFS is defined as time in weeks from randomization to the first documentation of objective tumor progression or death due to any cause. PFS was calculated as = (first event date minus randomization date plus 1) divided by 7. Tumor progression was determined from oncologic assessment data (where data meet the criteria for progressive disease \[PD\]), or from adverse event (AE) data (where the outcome was "Death").
Outcome measures
| Measure |
PF-00299804 (Adenocarcinoma Histology)
n=50 Participants
Participants with adenocarcinoma histology received PF-00299804 tablet 45 milligram (mg) orally once daily in cycles of 21 days until unacceptable toxicity, tumor progression, death, withdrawal from the study or investigator's discretion.
|
PF-00299804 (Non-adenocarcinoma Histology)
n=16 Participants
Participants with non-adenocarcinoma histology received PF-00299804 tablet 45 mg orally once daily in cycles of 21 days until unacceptable toxicity, tumor progression, death, withdrawal from the study or investigator's discretion.
|
|---|---|---|
|
Percentage of Participants With Progression-free Survival (PFS)
|
24.3 percentage of participants
Interval 12.4 to 38.4
|
8.0 percentage of participants
Interval 0.5 to 29.8
|
Adverse Events
PF-00299804 (Adenocarcinoma Histology)
PF-00299804 (Non-adenocarcinoma Histology)
Serious adverse events
| Measure |
PF-00299804 (Adenocarcinoma Histology)
n=50 participants at risk
Participants with adenocarcinoma histology received PF-00299804 tablet 45 milligram (mg) orally once daily in cycles of 21 days until unacceptable toxicity, tumor progression, death, withdrawal from the study or investigator's discretion.
|
PF-00299804 (Non-adenocarcinoma Histology)
n=16 participants at risk
Participants with non-adenocarcinoma histology received PF-00299804 tablet 45 mg orally once daily in cycles of 21 days until unacceptable toxicity, tumor progression, death, withdrawal from the study or investigator's discretion.
|
|---|---|---|
|
Blood and lymphatic system disorders
Anaemia
|
2.0%
1/50
The same event may appear as both an AE and a SAE. However, what is presented are distinct events. An event may be categorized as serious in one subject and as nonserious in another subject, or one subject may have experienced both a serious and nonserious event during the study.
|
0.00%
0/16
The same event may appear as both an AE and a SAE. However, what is presented are distinct events. An event may be categorized as serious in one subject and as nonserious in another subject, or one subject may have experienced both a serious and nonserious event during the study.
|
|
Gastrointestinal disorders
Abdominal pain
|
0.00%
0/50
The same event may appear as both an AE and a SAE. However, what is presented are distinct events. An event may be categorized as serious in one subject and as nonserious in another subject, or one subject may have experienced both a serious and nonserious event during the study.
|
12.5%
2/16
The same event may appear as both an AE and a SAE. However, what is presented are distinct events. An event may be categorized as serious in one subject and as nonserious in another subject, or one subject may have experienced both a serious and nonserious event during the study.
|
|
Gastrointestinal disorders
Constipation
|
0.00%
0/50
The same event may appear as both an AE and a SAE. However, what is presented are distinct events. An event may be categorized as serious in one subject and as nonserious in another subject, or one subject may have experienced both a serious and nonserious event during the study.
|
12.5%
2/16
The same event may appear as both an AE and a SAE. However, what is presented are distinct events. An event may be categorized as serious in one subject and as nonserious in another subject, or one subject may have experienced both a serious and nonserious event during the study.
|
|
Gastrointestinal disorders
Diarrhoea
|
2.0%
1/50
The same event may appear as both an AE and a SAE. However, what is presented are distinct events. An event may be categorized as serious in one subject and as nonserious in another subject, or one subject may have experienced both a serious and nonserious event during the study.
|
0.00%
0/16
The same event may appear as both an AE and a SAE. However, what is presented are distinct events. An event may be categorized as serious in one subject and as nonserious in another subject, or one subject may have experienced both a serious and nonserious event during the study.
|
|
Gastrointestinal disorders
Nausea
|
0.00%
0/50
The same event may appear as both an AE and a SAE. However, what is presented are distinct events. An event may be categorized as serious in one subject and as nonserious in another subject, or one subject may have experienced both a serious and nonserious event during the study.
|
6.2%
1/16
The same event may appear as both an AE and a SAE. However, what is presented are distinct events. An event may be categorized as serious in one subject and as nonserious in another subject, or one subject may have experienced both a serious and nonserious event during the study.
|
|
Gastrointestinal disorders
Pancreatitis
|
0.00%
0/50
The same event may appear as both an AE and a SAE. However, what is presented are distinct events. An event may be categorized as serious in one subject and as nonserious in another subject, or one subject may have experienced both a serious and nonserious event during the study.
|
6.2%
1/16
The same event may appear as both an AE and a SAE. However, what is presented are distinct events. An event may be categorized as serious in one subject and as nonserious in another subject, or one subject may have experienced both a serious and nonserious event during the study.
|
|
Gastrointestinal disorders
Vomiting
|
2.0%
1/50
The same event may appear as both an AE and a SAE. However, what is presented are distinct events. An event may be categorized as serious in one subject and as nonserious in another subject, or one subject may have experienced both a serious and nonserious event during the study.
|
6.2%
1/16
The same event may appear as both an AE and a SAE. However, what is presented are distinct events. An event may be categorized as serious in one subject and as nonserious in another subject, or one subject may have experienced both a serious and nonserious event during the study.
|
|
General disorders
Asthenia
|
0.00%
0/50
The same event may appear as both an AE and a SAE. However, what is presented are distinct events. An event may be categorized as serious in one subject and as nonserious in another subject, or one subject may have experienced both a serious and nonserious event during the study.
|
6.2%
1/16
The same event may appear as both an AE and a SAE. However, what is presented are distinct events. An event may be categorized as serious in one subject and as nonserious in another subject, or one subject may have experienced both a serious and nonserious event during the study.
|
|
General disorders
Disease progression
|
6.0%
3/50
The same event may appear as both an AE and a SAE. However, what is presented are distinct events. An event may be categorized as serious in one subject and as nonserious in another subject, or one subject may have experienced both a serious and nonserious event during the study.
|
0.00%
0/16
The same event may appear as both an AE and a SAE. However, what is presented are distinct events. An event may be categorized as serious in one subject and as nonserious in another subject, or one subject may have experienced both a serious and nonserious event during the study.
|
|
Infections and infestations
Cystitis
|
0.00%
0/50
The same event may appear as both an AE and a SAE. However, what is presented are distinct events. An event may be categorized as serious in one subject and as nonserious in another subject, or one subject may have experienced both a serious and nonserious event during the study.
|
6.2%
1/16
The same event may appear as both an AE and a SAE. However, what is presented are distinct events. An event may be categorized as serious in one subject and as nonserious in another subject, or one subject may have experienced both a serious and nonserious event during the study.
|
|
Infections and infestations
Pneumonia
|
2.0%
1/50
The same event may appear as both an AE and a SAE. However, what is presented are distinct events. An event may be categorized as serious in one subject and as nonserious in another subject, or one subject may have experienced both a serious and nonserious event during the study.
|
0.00%
0/16
The same event may appear as both an AE and a SAE. However, what is presented are distinct events. An event may be categorized as serious in one subject and as nonserious in another subject, or one subject may have experienced both a serious and nonserious event during the study.
|
|
Injury, poisoning and procedural complications
Hip fracture
|
0.00%
0/50
The same event may appear as both an AE and a SAE. However, what is presented are distinct events. An event may be categorized as serious in one subject and as nonserious in another subject, or one subject may have experienced both a serious and nonserious event during the study.
|
6.2%
1/16
The same event may appear as both an AE and a SAE. However, what is presented are distinct events. An event may be categorized as serious in one subject and as nonserious in another subject, or one subject may have experienced both a serious and nonserious event during the study.
|
|
Injury, poisoning and procedural complications
Spinal compression fracture
|
0.00%
0/50
The same event may appear as both an AE and a SAE. However, what is presented are distinct events. An event may be categorized as serious in one subject and as nonserious in another subject, or one subject may have experienced both a serious and nonserious event during the study.
|
6.2%
1/16
The same event may appear as both an AE and a SAE. However, what is presented are distinct events. An event may be categorized as serious in one subject and as nonserious in another subject, or one subject may have experienced both a serious and nonserious event during the study.
|
|
Metabolism and nutrition disorders
Dehydration
|
2.0%
1/50
The same event may appear as both an AE and a SAE. However, what is presented are distinct events. An event may be categorized as serious in one subject and as nonserious in another subject, or one subject may have experienced both a serious and nonserious event during the study.
|
0.00%
0/16
The same event may appear as both an AE and a SAE. However, what is presented are distinct events. An event may be categorized as serious in one subject and as nonserious in another subject, or one subject may have experienced both a serious and nonserious event during the study.
|
|
Metabolism and nutrition disorders
Hypercalcaemia
|
0.00%
0/50
The same event may appear as both an AE and a SAE. However, what is presented are distinct events. An event may be categorized as serious in one subject and as nonserious in another subject, or one subject may have experienced both a serious and nonserious event during the study.
|
6.2%
1/16
The same event may appear as both an AE and a SAE. However, what is presented are distinct events. An event may be categorized as serious in one subject and as nonserious in another subject, or one subject may have experienced both a serious and nonserious event during the study.
|
|
Neoplasms benign, malignant and unspecified (incl cysts and polyps)
Non-small cell lung cancer
|
0.00%
0/50
The same event may appear as both an AE and a SAE. However, what is presented are distinct events. An event may be categorized as serious in one subject and as nonserious in another subject, or one subject may have experienced both a serious and nonserious event during the study.
|
6.2%
1/16
The same event may appear as both an AE and a SAE. However, what is presented are distinct events. An event may be categorized as serious in one subject and as nonserious in another subject, or one subject may have experienced both a serious and nonserious event during the study.
|
|
Renal and urinary disorders
Renal failure acute
|
2.0%
1/50
The same event may appear as both an AE and a SAE. However, what is presented are distinct events. An event may be categorized as serious in one subject and as nonserious in another subject, or one subject may have experienced both a serious and nonserious event during the study.
|
0.00%
0/16
The same event may appear as both an AE and a SAE. However, what is presented are distinct events. An event may be categorized as serious in one subject and as nonserious in another subject, or one subject may have experienced both a serious and nonserious event during the study.
|
|
Respiratory, thoracic and mediastinal disorders
Dyspnoea
|
2.0%
1/50
The same event may appear as both an AE and a SAE. However, what is presented are distinct events. An event may be categorized as serious in one subject and as nonserious in another subject, or one subject may have experienced both a serious and nonserious event during the study.
|
6.2%
1/16
The same event may appear as both an AE and a SAE. However, what is presented are distinct events. An event may be categorized as serious in one subject and as nonserious in another subject, or one subject may have experienced both a serious and nonserious event during the study.
|
|
Respiratory, thoracic and mediastinal disorders
Haemoptysis
|
0.00%
0/50
The same event may appear as both an AE and a SAE. However, what is presented are distinct events. An event may be categorized as serious in one subject and as nonserious in another subject, or one subject may have experienced both a serious and nonserious event during the study.
|
6.2%
1/16
The same event may appear as both an AE and a SAE. However, what is presented are distinct events. An event may be categorized as serious in one subject and as nonserious in another subject, or one subject may have experienced both a serious and nonserious event during the study.
|
|
Respiratory, thoracic and mediastinal disorders
Hypoxia
|
0.00%
0/50
The same event may appear as both an AE and a SAE. However, what is presented are distinct events. An event may be categorized as serious in one subject and as nonserious in another subject, or one subject may have experienced both a serious and nonserious event during the study.
|
6.2%
1/16
The same event may appear as both an AE and a SAE. However, what is presented are distinct events. An event may be categorized as serious in one subject and as nonserious in another subject, or one subject may have experienced both a serious and nonserious event during the study.
|
|
Respiratory, thoracic and mediastinal disorders
Pneumonia aspiration
|
2.0%
1/50
The same event may appear as both an AE and a SAE. However, what is presented are distinct events. An event may be categorized as serious in one subject and as nonserious in another subject, or one subject may have experienced both a serious and nonserious event during the study.
|
0.00%
0/16
The same event may appear as both an AE and a SAE. However, what is presented are distinct events. An event may be categorized as serious in one subject and as nonserious in another subject, or one subject may have experienced both a serious and nonserious event during the study.
|
|
Respiratory, thoracic and mediastinal disorders
Pulmonary embolism
|
4.0%
2/50
The same event may appear as both an AE and a SAE. However, what is presented are distinct events. An event may be categorized as serious in one subject and as nonserious in another subject, or one subject may have experienced both a serious and nonserious event during the study.
|
0.00%
0/16
The same event may appear as both an AE and a SAE. However, what is presented are distinct events. An event may be categorized as serious in one subject and as nonserious in another subject, or one subject may have experienced both a serious and nonserious event during the study.
|
|
Respiratory, thoracic and mediastinal disorders
Respiratory failure
|
6.0%
3/50
The same event may appear as both an AE and a SAE. However, what is presented are distinct events. An event may be categorized as serious in one subject and as nonserious in another subject, or one subject may have experienced both a serious and nonserious event during the study.
|
0.00%
0/16
The same event may appear as both an AE and a SAE. However, what is presented are distinct events. An event may be categorized as serious in one subject and as nonserious in another subject, or one subject may have experienced both a serious and nonserious event during the study.
|
|
Vascular disorders
Hypotension
|
0.00%
0/50
The same event may appear as both an AE and a SAE. However, what is presented are distinct events. An event may be categorized as serious in one subject and as nonserious in another subject, or one subject may have experienced both a serious and nonserious event during the study.
|
6.2%
1/16
The same event may appear as both an AE and a SAE. However, what is presented are distinct events. An event may be categorized as serious in one subject and as nonserious in another subject, or one subject may have experienced both a serious and nonserious event during the study.
|
Other adverse events
| Measure |
PF-00299804 (Adenocarcinoma Histology)
n=50 participants at risk
Participants with adenocarcinoma histology received PF-00299804 tablet 45 milligram (mg) orally once daily in cycles of 21 days until unacceptable toxicity, tumor progression, death, withdrawal from the study or investigator's discretion.
|
PF-00299804 (Non-adenocarcinoma Histology)
n=16 participants at risk
Participants with non-adenocarcinoma histology received PF-00299804 tablet 45 mg orally once daily in cycles of 21 days until unacceptable toxicity, tumor progression, death, withdrawal from the study or investigator's discretion.
|
|---|---|---|
|
Blood and lymphatic system disorders
Anaemia
|
6.0%
3/50
The same event may appear as both an AE and a SAE. However, what is presented are distinct events. An event may be categorized as serious in one subject and as nonserious in another subject, or one subject may have experienced both a serious and nonserious event during the study.
|
12.5%
2/16
The same event may appear as both an AE and a SAE. However, what is presented are distinct events. An event may be categorized as serious in one subject and as nonserious in another subject, or one subject may have experienced both a serious and nonserious event during the study.
|
|
Blood and lymphatic system disorders
Leukopenia
|
4.0%
2/50
The same event may appear as both an AE and a SAE. However, what is presented are distinct events. An event may be categorized as serious in one subject and as nonserious in another subject, or one subject may have experienced both a serious and nonserious event during the study.
|
6.2%
1/16
The same event may appear as both an AE and a SAE. However, what is presented are distinct events. An event may be categorized as serious in one subject and as nonserious in another subject, or one subject may have experienced both a serious and nonserious event during the study.
|
|
Blood and lymphatic system disorders
Lymphopenia
|
2.0%
1/50
The same event may appear as both an AE and a SAE. However, what is presented are distinct events. An event may be categorized as serious in one subject and as nonserious in another subject, or one subject may have experienced both a serious and nonserious event during the study.
|
0.00%
0/16
The same event may appear as both an AE and a SAE. However, what is presented are distinct events. An event may be categorized as serious in one subject and as nonserious in another subject, or one subject may have experienced both a serious and nonserious event during the study.
|
|
Blood and lymphatic system disorders
Neutropenia
|
2.0%
1/50
The same event may appear as both an AE and a SAE. However, what is presented are distinct events. An event may be categorized as serious in one subject and as nonserious in another subject, or one subject may have experienced both a serious and nonserious event during the study.
|
0.00%
0/16
The same event may appear as both an AE and a SAE. However, what is presented are distinct events. An event may be categorized as serious in one subject and as nonserious in another subject, or one subject may have experienced both a serious and nonserious event during the study.
|
|
Cardiac disorders
Nodal rhythm
|
0.00%
0/50
The same event may appear as both an AE and a SAE. However, what is presented are distinct events. An event may be categorized as serious in one subject and as nonserious in another subject, or one subject may have experienced both a serious and nonserious event during the study.
|
6.2%
1/16
The same event may appear as both an AE and a SAE. However, what is presented are distinct events. An event may be categorized as serious in one subject and as nonserious in another subject, or one subject may have experienced both a serious and nonserious event during the study.
|
|
Cardiac disorders
Tachycardia
|
2.0%
1/50
The same event may appear as both an AE and a SAE. However, what is presented are distinct events. An event may be categorized as serious in one subject and as nonserious in another subject, or one subject may have experienced both a serious and nonserious event during the study.
|
12.5%
2/16
The same event may appear as both an AE and a SAE. However, what is presented are distinct events. An event may be categorized as serious in one subject and as nonserious in another subject, or one subject may have experienced both a serious and nonserious event during the study.
|
|
Eye disorders
Blepharitis
|
4.0%
2/50
The same event may appear as both an AE and a SAE. However, what is presented are distinct events. An event may be categorized as serious in one subject and as nonserious in another subject, or one subject may have experienced both a serious and nonserious event during the study.
|
6.2%
1/16
The same event may appear as both an AE and a SAE. However, what is presented are distinct events. An event may be categorized as serious in one subject and as nonserious in another subject, or one subject may have experienced both a serious and nonserious event during the study.
|
|
Eye disorders
Conjunctivitis
|
6.0%
3/50
The same event may appear as both an AE and a SAE. However, what is presented are distinct events. An event may be categorized as serious in one subject and as nonserious in another subject, or one subject may have experienced both a serious and nonserious event during the study.
|
6.2%
1/16
The same event may appear as both an AE and a SAE. However, what is presented are distinct events. An event may be categorized as serious in one subject and as nonserious in another subject, or one subject may have experienced both a serious and nonserious event during the study.
|
|
Eye disorders
Dry eye
|
2.0%
1/50
The same event may appear as both an AE and a SAE. However, what is presented are distinct events. An event may be categorized as serious in one subject and as nonserious in another subject, or one subject may have experienced both a serious and nonserious event during the study.
|
12.5%
2/16
The same event may appear as both an AE and a SAE. However, what is presented are distinct events. An event may be categorized as serious in one subject and as nonserious in another subject, or one subject may have experienced both a serious and nonserious event during the study.
|
|
Eye disorders
Eye discharge
|
4.0%
2/50
The same event may appear as both an AE and a SAE. However, what is presented are distinct events. An event may be categorized as serious in one subject and as nonserious in another subject, or one subject may have experienced both a serious and nonserious event during the study.
|
0.00%
0/16
The same event may appear as both an AE and a SAE. However, what is presented are distinct events. An event may be categorized as serious in one subject and as nonserious in another subject, or one subject may have experienced both a serious and nonserious event during the study.
|
|
Eye disorders
Eye pruritus
|
4.0%
2/50
The same event may appear as both an AE and a SAE. However, what is presented are distinct events. An event may be categorized as serious in one subject and as nonserious in another subject, or one subject may have experienced both a serious and nonserious event during the study.
|
0.00%
0/16
The same event may appear as both an AE and a SAE. However, what is presented are distinct events. An event may be categorized as serious in one subject and as nonserious in another subject, or one subject may have experienced both a serious and nonserious event during the study.
|
|
Eye disorders
Ocular hyperaemia
|
0.00%
0/50
The same event may appear as both an AE and a SAE. However, what is presented are distinct events. An event may be categorized as serious in one subject and as nonserious in another subject, or one subject may have experienced both a serious and nonserious event during the study.
|
6.2%
1/16
The same event may appear as both an AE and a SAE. However, what is presented are distinct events. An event may be categorized as serious in one subject and as nonserious in another subject, or one subject may have experienced both a serious and nonserious event during the study.
|
|
Eye disorders
Vitreous floaters
|
0.00%
0/50
The same event may appear as both an AE and a SAE. However, what is presented are distinct events. An event may be categorized as serious in one subject and as nonserious in another subject, or one subject may have experienced both a serious and nonserious event during the study.
|
6.2%
1/16
The same event may appear as both an AE and a SAE. However, what is presented are distinct events. An event may be categorized as serious in one subject and as nonserious in another subject, or one subject may have experienced both a serious and nonserious event during the study.
|
|
Gastrointestinal disorders
Abdominal discomfort
|
2.0%
1/50
The same event may appear as both an AE and a SAE. However, what is presented are distinct events. An event may be categorized as serious in one subject and as nonserious in another subject, or one subject may have experienced both a serious and nonserious event during the study.
|
0.00%
0/16
The same event may appear as both an AE and a SAE. However, what is presented are distinct events. An event may be categorized as serious in one subject and as nonserious in another subject, or one subject may have experienced both a serious and nonserious event during the study.
|
|
Gastrointestinal disorders
Abdominal pain
|
8.0%
4/50
The same event may appear as both an AE and a SAE. However, what is presented are distinct events. An event may be categorized as serious in one subject and as nonserious in another subject, or one subject may have experienced both a serious and nonserious event during the study.
|
0.00%
0/16
The same event may appear as both an AE and a SAE. However, what is presented are distinct events. An event may be categorized as serious in one subject and as nonserious in another subject, or one subject may have experienced both a serious and nonserious event during the study.
|
|
Gastrointestinal disorders
Abdominal pain upper
|
2.0%
1/50
The same event may appear as both an AE and a SAE. However, what is presented are distinct events. An event may be categorized as serious in one subject and as nonserious in another subject, or one subject may have experienced both a serious and nonserious event during the study.
|
6.2%
1/16
The same event may appear as both an AE and a SAE. However, what is presented are distinct events. An event may be categorized as serious in one subject and as nonserious in another subject, or one subject may have experienced both a serious and nonserious event during the study.
|
|
Gastrointestinal disorders
Ascites
|
2.0%
1/50
The same event may appear as both an AE and a SAE. However, what is presented are distinct events. An event may be categorized as serious in one subject and as nonserious in another subject, or one subject may have experienced both a serious and nonserious event during the study.
|
0.00%
0/16
The same event may appear as both an AE and a SAE. However, what is presented are distinct events. An event may be categorized as serious in one subject and as nonserious in another subject, or one subject may have experienced both a serious and nonserious event during the study.
|
|
Gastrointestinal disorders
Atrophic glossitis
|
0.00%
0/50
The same event may appear as both an AE and a SAE. However, what is presented are distinct events. An event may be categorized as serious in one subject and as nonserious in another subject, or one subject may have experienced both a serious and nonserious event during the study.
|
6.2%
1/16
The same event may appear as both an AE and a SAE. However, what is presented are distinct events. An event may be categorized as serious in one subject and as nonserious in another subject, or one subject may have experienced both a serious and nonserious event during the study.
|
|
Gastrointestinal disorders
Chapped lips
|
2.0%
1/50
The same event may appear as both an AE and a SAE. However, what is presented are distinct events. An event may be categorized as serious in one subject and as nonserious in another subject, or one subject may have experienced both a serious and nonserious event during the study.
|
0.00%
0/16
The same event may appear as both an AE and a SAE. However, what is presented are distinct events. An event may be categorized as serious in one subject and as nonserious in another subject, or one subject may have experienced both a serious and nonserious event during the study.
|
|
Gastrointestinal disorders
Cheilitis
|
10.0%
5/50
The same event may appear as both an AE and a SAE. However, what is presented are distinct events. An event may be categorized as serious in one subject and as nonserious in another subject, or one subject may have experienced both a serious and nonserious event during the study.
|
0.00%
0/16
The same event may appear as both an AE and a SAE. However, what is presented are distinct events. An event may be categorized as serious in one subject and as nonserious in another subject, or one subject may have experienced both a serious and nonserious event during the study.
|
|
Gastrointestinal disorders
Constipation
|
10.0%
5/50
The same event may appear as both an AE and a SAE. However, what is presented are distinct events. An event may be categorized as serious in one subject and as nonserious in another subject, or one subject may have experienced both a serious and nonserious event during the study.
|
6.2%
1/16
The same event may appear as both an AE and a SAE. However, what is presented are distinct events. An event may be categorized as serious in one subject and as nonserious in another subject, or one subject may have experienced both a serious and nonserious event during the study.
|
|
Gastrointestinal disorders
Diarrhoea
|
88.0%
44/50
The same event may appear as both an AE and a SAE. However, what is presented are distinct events. An event may be categorized as serious in one subject and as nonserious in another subject, or one subject may have experienced both a serious and nonserious event during the study.
|
81.2%
13/16
The same event may appear as both an AE and a SAE. However, what is presented are distinct events. An event may be categorized as serious in one subject and as nonserious in another subject, or one subject may have experienced both a serious and nonserious event during the study.
|
|
Gastrointestinal disorders
Diarrhoea haemorrhagic
|
0.00%
0/50
The same event may appear as both an AE and a SAE. However, what is presented are distinct events. An event may be categorized as serious in one subject and as nonserious in another subject, or one subject may have experienced both a serious and nonserious event during the study.
|
6.2%
1/16
The same event may appear as both an AE and a SAE. However, what is presented are distinct events. An event may be categorized as serious in one subject and as nonserious in another subject, or one subject may have experienced both a serious and nonserious event during the study.
|
|
Gastrointestinal disorders
Dry mouth
|
2.0%
1/50
The same event may appear as both an AE and a SAE. However, what is presented are distinct events. An event may be categorized as serious in one subject and as nonserious in another subject, or one subject may have experienced both a serious and nonserious event during the study.
|
0.00%
0/16
The same event may appear as both an AE and a SAE. However, what is presented are distinct events. An event may be categorized as serious in one subject and as nonserious in another subject, or one subject may have experienced both a serious and nonserious event during the study.
|
|
Gastrointestinal disorders
Dyspepsia
|
2.0%
1/50
The same event may appear as both an AE and a SAE. However, what is presented are distinct events. An event may be categorized as serious in one subject and as nonserious in another subject, or one subject may have experienced both a serious and nonserious event during the study.
|
0.00%
0/16
The same event may appear as both an AE and a SAE. However, what is presented are distinct events. An event may be categorized as serious in one subject and as nonserious in another subject, or one subject may have experienced both a serious and nonserious event during the study.
|
|
Gastrointestinal disorders
Dysphagia
|
4.0%
2/50
The same event may appear as both an AE and a SAE. However, what is presented are distinct events. An event may be categorized as serious in one subject and as nonserious in another subject, or one subject may have experienced both a serious and nonserious event during the study.
|
0.00%
0/16
The same event may appear as both an AE and a SAE. However, what is presented are distinct events. An event may be categorized as serious in one subject and as nonserious in another subject, or one subject may have experienced both a serious and nonserious event during the study.
|
|
Gastrointestinal disorders
Faeces discoloured
|
2.0%
1/50
The same event may appear as both an AE and a SAE. However, what is presented are distinct events. An event may be categorized as serious in one subject and as nonserious in another subject, or one subject may have experienced both a serious and nonserious event during the study.
|
0.00%
0/16
The same event may appear as both an AE and a SAE. However, what is presented are distinct events. An event may be categorized as serious in one subject and as nonserious in another subject, or one subject may have experienced both a serious and nonserious event during the study.
|
|
Gastrointestinal disorders
Gastritis
|
2.0%
1/50
The same event may appear as both an AE and a SAE. However, what is presented are distinct events. An event may be categorized as serious in one subject and as nonserious in another subject, or one subject may have experienced both a serious and nonserious event during the study.
|
12.5%
2/16
The same event may appear as both an AE and a SAE. However, what is presented are distinct events. An event may be categorized as serious in one subject and as nonserious in another subject, or one subject may have experienced both a serious and nonserious event during the study.
|
|
Gastrointestinal disorders
Gastrointestinal haemorrhage
|
0.00%
0/50
The same event may appear as both an AE and a SAE. However, what is presented are distinct events. An event may be categorized as serious in one subject and as nonserious in another subject, or one subject may have experienced both a serious and nonserious event during the study.
|
6.2%
1/16
The same event may appear as both an AE and a SAE. However, what is presented are distinct events. An event may be categorized as serious in one subject and as nonserious in another subject, or one subject may have experienced both a serious and nonserious event during the study.
|
|
Gastrointestinal disorders
Gingival pain
|
0.00%
0/50
The same event may appear as both an AE and a SAE. However, what is presented are distinct events. An event may be categorized as serious in one subject and as nonserious in another subject, or one subject may have experienced both a serious and nonserious event during the study.
|
6.2%
1/16
The same event may appear as both an AE and a SAE. However, what is presented are distinct events. An event may be categorized as serious in one subject and as nonserious in another subject, or one subject may have experienced both a serious and nonserious event during the study.
|
|
Gastrointestinal disorders
Glossodynia
|
4.0%
2/50
The same event may appear as both an AE and a SAE. However, what is presented are distinct events. An event may be categorized as serious in one subject and as nonserious in another subject, or one subject may have experienced both a serious and nonserious event during the study.
|
0.00%
0/16
The same event may appear as both an AE and a SAE. However, what is presented are distinct events. An event may be categorized as serious in one subject and as nonserious in another subject, or one subject may have experienced both a serious and nonserious event during the study.
|
|
Gastrointestinal disorders
Haemorrhoids
|
4.0%
2/50
The same event may appear as both an AE and a SAE. However, what is presented are distinct events. An event may be categorized as serious in one subject and as nonserious in another subject, or one subject may have experienced both a serious and nonserious event during the study.
|
0.00%
0/16
The same event may appear as both an AE and a SAE. However, what is presented are distinct events. An event may be categorized as serious in one subject and as nonserious in another subject, or one subject may have experienced both a serious and nonserious event during the study.
|
|
Gastrointestinal disorders
Lip dry
|
2.0%
1/50
The same event may appear as both an AE and a SAE. However, what is presented are distinct events. An event may be categorized as serious in one subject and as nonserious in another subject, or one subject may have experienced both a serious and nonserious event during the study.
|
0.00%
0/16
The same event may appear as both an AE and a SAE. However, what is presented are distinct events. An event may be categorized as serious in one subject and as nonserious in another subject, or one subject may have experienced both a serious and nonserious event during the study.
|
|
Gastrointestinal disorders
Lip ulceration
|
2.0%
1/50
The same event may appear as both an AE and a SAE. However, what is presented are distinct events. An event may be categorized as serious in one subject and as nonserious in another subject, or one subject may have experienced both a serious and nonserious event during the study.
|
0.00%
0/16
The same event may appear as both an AE and a SAE. However, what is presented are distinct events. An event may be categorized as serious in one subject and as nonserious in another subject, or one subject may have experienced both a serious and nonserious event during the study.
|
|
Gastrointestinal disorders
Nausea
|
24.0%
12/50
The same event may appear as both an AE and a SAE. However, what is presented are distinct events. An event may be categorized as serious in one subject and as nonserious in another subject, or one subject may have experienced both a serious and nonserious event during the study.
|
37.5%
6/16
The same event may appear as both an AE and a SAE. However, what is presented are distinct events. An event may be categorized as serious in one subject and as nonserious in another subject, or one subject may have experienced both a serious and nonserious event during the study.
|
|
Gastrointestinal disorders
Oral pain
|
4.0%
2/50
The same event may appear as both an AE and a SAE. However, what is presented are distinct events. An event may be categorized as serious in one subject and as nonserious in another subject, or one subject may have experienced both a serious and nonserious event during the study.
|
0.00%
0/16
The same event may appear as both an AE and a SAE. However, what is presented are distinct events. An event may be categorized as serious in one subject and as nonserious in another subject, or one subject may have experienced both a serious and nonserious event during the study.
|
|
Gastrointestinal disorders
Stomatitis
|
26.0%
13/50
The same event may appear as both an AE and a SAE. However, what is presented are distinct events. An event may be categorized as serious in one subject and as nonserious in another subject, or one subject may have experienced both a serious and nonserious event during the study.
|
18.8%
3/16
The same event may appear as both an AE and a SAE. However, what is presented are distinct events. An event may be categorized as serious in one subject and as nonserious in another subject, or one subject may have experienced both a serious and nonserious event during the study.
|
|
Gastrointestinal disorders
Swollen tongue
|
2.0%
1/50
The same event may appear as both an AE and a SAE. However, what is presented are distinct events. An event may be categorized as serious in one subject and as nonserious in another subject, or one subject may have experienced both a serious and nonserious event during the study.
|
0.00%
0/16
The same event may appear as both an AE and a SAE. However, what is presented are distinct events. An event may be categorized as serious in one subject and as nonserious in another subject, or one subject may have experienced both a serious and nonserious event during the study.
|
|
Gastrointestinal disorders
Tongue coated
|
0.00%
0/50
The same event may appear as both an AE and a SAE. However, what is presented are distinct events. An event may be categorized as serious in one subject and as nonserious in another subject, or one subject may have experienced both a serious and nonserious event during the study.
|
6.2%
1/16
The same event may appear as both an AE and a SAE. However, what is presented are distinct events. An event may be categorized as serious in one subject and as nonserious in another subject, or one subject may have experienced both a serious and nonserious event during the study.
|
|
Gastrointestinal disorders
Tongue dry
|
2.0%
1/50
The same event may appear as both an AE and a SAE. However, what is presented are distinct events. An event may be categorized as serious in one subject and as nonserious in another subject, or one subject may have experienced both a serious and nonserious event during the study.
|
0.00%
0/16
The same event may appear as both an AE and a SAE. However, what is presented are distinct events. An event may be categorized as serious in one subject and as nonserious in another subject, or one subject may have experienced both a serious and nonserious event during the study.
|
|
Gastrointestinal disorders
Vomiting
|
22.0%
11/50
The same event may appear as both an AE and a SAE. However, what is presented are distinct events. An event may be categorized as serious in one subject and as nonserious in another subject, or one subject may have experienced both a serious and nonserious event during the study.
|
18.8%
3/16
The same event may appear as both an AE and a SAE. However, what is presented are distinct events. An event may be categorized as serious in one subject and as nonserious in another subject, or one subject may have experienced both a serious and nonserious event during the study.
|
|
General disorders
Asthenia
|
2.0%
1/50
The same event may appear as both an AE and a SAE. However, what is presented are distinct events. An event may be categorized as serious in one subject and as nonserious in another subject, or one subject may have experienced both a serious and nonserious event during the study.
|
0.00%
0/16
The same event may appear as both an AE and a SAE. However, what is presented are distinct events. An event may be categorized as serious in one subject and as nonserious in another subject, or one subject may have experienced both a serious and nonserious event during the study.
|
|
General disorders
Chest discomfort
|
0.00%
0/50
The same event may appear as both an AE and a SAE. However, what is presented are distinct events. An event may be categorized as serious in one subject and as nonserious in another subject, or one subject may have experienced both a serious and nonserious event during the study.
|
6.2%
1/16
The same event may appear as both an AE and a SAE. However, what is presented are distinct events. An event may be categorized as serious in one subject and as nonserious in another subject, or one subject may have experienced both a serious and nonserious event during the study.
|
|
General disorders
Chest pain
|
8.0%
4/50
The same event may appear as both an AE and a SAE. However, what is presented are distinct events. An event may be categorized as serious in one subject and as nonserious in another subject, or one subject may have experienced both a serious and nonserious event during the study.
|
6.2%
1/16
The same event may appear as both an AE and a SAE. However, what is presented are distinct events. An event may be categorized as serious in one subject and as nonserious in another subject, or one subject may have experienced both a serious and nonserious event during the study.
|
|
General disorders
Chills
|
2.0%
1/50
The same event may appear as both an AE and a SAE. However, what is presented are distinct events. An event may be categorized as serious in one subject and as nonserious in another subject, or one subject may have experienced both a serious and nonserious event during the study.
|
0.00%
0/16
The same event may appear as both an AE and a SAE. However, what is presented are distinct events. An event may be categorized as serious in one subject and as nonserious in another subject, or one subject may have experienced both a serious and nonserious event during the study.
|
|
General disorders
Fatigue
|
62.0%
31/50
The same event may appear as both an AE and a SAE. However, what is presented are distinct events. An event may be categorized as serious in one subject and as nonserious in another subject, or one subject may have experienced both a serious and nonserious event during the study.
|
43.8%
7/16
The same event may appear as both an AE and a SAE. However, what is presented are distinct events. An event may be categorized as serious in one subject and as nonserious in another subject, or one subject may have experienced both a serious and nonserious event during the study.
|
|
General disorders
Gait disturbance
|
2.0%
1/50
The same event may appear as both an AE and a SAE. However, what is presented are distinct events. An event may be categorized as serious in one subject and as nonserious in another subject, or one subject may have experienced both a serious and nonserious event during the study.
|
6.2%
1/16
The same event may appear as both an AE and a SAE. However, what is presented are distinct events. An event may be categorized as serious in one subject and as nonserious in another subject, or one subject may have experienced both a serious and nonserious event during the study.
|
|
General disorders
Injection site pain
|
2.0%
1/50
The same event may appear as both an AE and a SAE. However, what is presented are distinct events. An event may be categorized as serious in one subject and as nonserious in another subject, or one subject may have experienced both a serious and nonserious event during the study.
|
0.00%
0/16
The same event may appear as both an AE and a SAE. However, what is presented are distinct events. An event may be categorized as serious in one subject and as nonserious in another subject, or one subject may have experienced both a serious and nonserious event during the study.
|
|
General disorders
Mass
|
2.0%
1/50
The same event may appear as both an AE and a SAE. However, what is presented are distinct events. An event may be categorized as serious in one subject and as nonserious in another subject, or one subject may have experienced both a serious and nonserious event during the study.
|
0.00%
0/16
The same event may appear as both an AE and a SAE. However, what is presented are distinct events. An event may be categorized as serious in one subject and as nonserious in another subject, or one subject may have experienced both a serious and nonserious event during the study.
|
|
General disorders
Mucosal inflammation
|
8.0%
4/50
The same event may appear as both an AE and a SAE. However, what is presented are distinct events. An event may be categorized as serious in one subject and as nonserious in another subject, or one subject may have experienced both a serious and nonserious event during the study.
|
18.8%
3/16
The same event may appear as both an AE and a SAE. However, what is presented are distinct events. An event may be categorized as serious in one subject and as nonserious in another subject, or one subject may have experienced both a serious and nonserious event during the study.
|
|
General disorders
Mucous membrane disorder
|
2.0%
1/50
The same event may appear as both an AE and a SAE. However, what is presented are distinct events. An event may be categorized as serious in one subject and as nonserious in another subject, or one subject may have experienced both a serious and nonserious event during the study.
|
0.00%
0/16
The same event may appear as both an AE and a SAE. However, what is presented are distinct events. An event may be categorized as serious in one subject and as nonserious in another subject, or one subject may have experienced both a serious and nonserious event during the study.
|
|
General disorders
Oedema
|
0.00%
0/50
The same event may appear as both an AE and a SAE. However, what is presented are distinct events. An event may be categorized as serious in one subject and as nonserious in another subject, or one subject may have experienced both a serious and nonserious event during the study.
|
6.2%
1/16
The same event may appear as both an AE and a SAE. However, what is presented are distinct events. An event may be categorized as serious in one subject and as nonserious in another subject, or one subject may have experienced both a serious and nonserious event during the study.
|
|
General disorders
Oedema peripheral
|
8.0%
4/50
The same event may appear as both an AE and a SAE. However, what is presented are distinct events. An event may be categorized as serious in one subject and as nonserious in another subject, or one subject may have experienced both a serious and nonserious event during the study.
|
12.5%
2/16
The same event may appear as both an AE and a SAE. However, what is presented are distinct events. An event may be categorized as serious in one subject and as nonserious in another subject, or one subject may have experienced both a serious and nonserious event during the study.
|
|
General disorders
Pain
|
6.0%
3/50
The same event may appear as both an AE and a SAE. However, what is presented are distinct events. An event may be categorized as serious in one subject and as nonserious in another subject, or one subject may have experienced both a serious and nonserious event during the study.
|
0.00%
0/16
The same event may appear as both an AE and a SAE. However, what is presented are distinct events. An event may be categorized as serious in one subject and as nonserious in another subject, or one subject may have experienced both a serious and nonserious event during the study.
|
|
General disorders
Pyrexia
|
2.0%
1/50
The same event may appear as both an AE and a SAE. However, what is presented are distinct events. An event may be categorized as serious in one subject and as nonserious in another subject, or one subject may have experienced both a serious and nonserious event during the study.
|
6.2%
1/16
The same event may appear as both an AE and a SAE. However, what is presented are distinct events. An event may be categorized as serious in one subject and as nonserious in another subject, or one subject may have experienced both a serious and nonserious event during the study.
|
|
Hepatobiliary disorders
Hepatic failure
|
2.0%
1/50
The same event may appear as both an AE and a SAE. However, what is presented are distinct events. An event may be categorized as serious in one subject and as nonserious in another subject, or one subject may have experienced both a serious and nonserious event during the study.
|
0.00%
0/16
The same event may appear as both an AE and a SAE. However, what is presented are distinct events. An event may be categorized as serious in one subject and as nonserious in another subject, or one subject may have experienced both a serious and nonserious event during the study.
|
|
Immune system disorders
Contrast media allergy
|
2.0%
1/50
The same event may appear as both an AE and a SAE. However, what is presented are distinct events. An event may be categorized as serious in one subject and as nonserious in another subject, or one subject may have experienced both a serious and nonserious event during the study.
|
0.00%
0/16
The same event may appear as both an AE and a SAE. However, what is presented are distinct events. An event may be categorized as serious in one subject and as nonserious in another subject, or one subject may have experienced both a serious and nonserious event during the study.
|
|
Immune system disorders
Hypersensitivity
|
2.0%
1/50
The same event may appear as both an AE and a SAE. However, what is presented are distinct events. An event may be categorized as serious in one subject and as nonserious in another subject, or one subject may have experienced both a serious and nonserious event during the study.
|
0.00%
0/16
The same event may appear as both an AE and a SAE. However, what is presented are distinct events. An event may be categorized as serious in one subject and as nonserious in another subject, or one subject may have experienced both a serious and nonserious event during the study.
|
|
Infections and infestations
Cellulitis
|
2.0%
1/50
The same event may appear as both an AE and a SAE. However, what is presented are distinct events. An event may be categorized as serious in one subject and as nonserious in another subject, or one subject may have experienced both a serious and nonserious event during the study.
|
0.00%
0/16
The same event may appear as both an AE and a SAE. However, what is presented are distinct events. An event may be categorized as serious in one subject and as nonserious in another subject, or one subject may have experienced both a serious and nonserious event during the study.
|
|
Infections and infestations
Folliculitis
|
2.0%
1/50
The same event may appear as both an AE and a SAE. However, what is presented are distinct events. An event may be categorized as serious in one subject and as nonserious in another subject, or one subject may have experienced both a serious and nonserious event during the study.
|
0.00%
0/16
The same event may appear as both an AE and a SAE. However, what is presented are distinct events. An event may be categorized as serious in one subject and as nonserious in another subject, or one subject may have experienced both a serious and nonserious event during the study.
|
|
Infections and infestations
Fungal skin infection
|
4.0%
2/50
The same event may appear as both an AE and a SAE. However, what is presented are distinct events. An event may be categorized as serious in one subject and as nonserious in another subject, or one subject may have experienced both a serious and nonserious event during the study.
|
6.2%
1/16
The same event may appear as both an AE and a SAE. However, what is presented are distinct events. An event may be categorized as serious in one subject and as nonserious in another subject, or one subject may have experienced both a serious and nonserious event during the study.
|
|
Infections and infestations
Localised infection
|
0.00%
0/50
The same event may appear as both an AE and a SAE. However, what is presented are distinct events. An event may be categorized as serious in one subject and as nonserious in another subject, or one subject may have experienced both a serious and nonserious event during the study.
|
6.2%
1/16
The same event may appear as both an AE and a SAE. However, what is presented are distinct events. An event may be categorized as serious in one subject and as nonserious in another subject, or one subject may have experienced both a serious and nonserious event during the study.
|
|
Infections and infestations
Nail infection
|
0.00%
0/50
The same event may appear as both an AE and a SAE. However, what is presented are distinct events. An event may be categorized as serious in one subject and as nonserious in another subject, or one subject may have experienced both a serious and nonserious event during the study.
|
6.2%
1/16
The same event may appear as both an AE and a SAE. However, what is presented are distinct events. An event may be categorized as serious in one subject and as nonserious in another subject, or one subject may have experienced both a serious and nonserious event during the study.
|
|
Infections and infestations
Oral fungal infection
|
2.0%
1/50
The same event may appear as both an AE and a SAE. However, what is presented are distinct events. An event may be categorized as serious in one subject and as nonserious in another subject, or one subject may have experienced both a serious and nonserious event during the study.
|
0.00%
0/16
The same event may appear as both an AE and a SAE. However, what is presented are distinct events. An event may be categorized as serious in one subject and as nonserious in another subject, or one subject may have experienced both a serious and nonserious event during the study.
|
|
Infections and infestations
Oral herpes
|
2.0%
1/50
The same event may appear as both an AE and a SAE. However, what is presented are distinct events. An event may be categorized as serious in one subject and as nonserious in another subject, or one subject may have experienced both a serious and nonserious event during the study.
|
0.00%
0/16
The same event may appear as both an AE and a SAE. However, what is presented are distinct events. An event may be categorized as serious in one subject and as nonserious in another subject, or one subject may have experienced both a serious and nonserious event during the study.
|
|
Infections and infestations
Paronychia
|
10.0%
5/50
The same event may appear as both an AE and a SAE. However, what is presented are distinct events. An event may be categorized as serious in one subject and as nonserious in another subject, or one subject may have experienced both a serious and nonserious event during the study.
|
12.5%
2/16
The same event may appear as both an AE and a SAE. However, what is presented are distinct events. An event may be categorized as serious in one subject and as nonserious in another subject, or one subject may have experienced both a serious and nonserious event during the study.
|
|
Infections and infestations
Pharyngitis
|
2.0%
1/50
The same event may appear as both an AE and a SAE. However, what is presented are distinct events. An event may be categorized as serious in one subject and as nonserious in another subject, or one subject may have experienced both a serious and nonserious event during the study.
|
0.00%
0/16
The same event may appear as both an AE and a SAE. However, what is presented are distinct events. An event may be categorized as serious in one subject and as nonserious in another subject, or one subject may have experienced both a serious and nonserious event during the study.
|
|
Infections and infestations
Pneumonia
|
2.0%
1/50
The same event may appear as both an AE and a SAE. However, what is presented are distinct events. An event may be categorized as serious in one subject and as nonserious in another subject, or one subject may have experienced both a serious and nonserious event during the study.
|
0.00%
0/16
The same event may appear as both an AE and a SAE. However, what is presented are distinct events. An event may be categorized as serious in one subject and as nonserious in another subject, or one subject may have experienced both a serious and nonserious event during the study.
|
|
Infections and infestations
Rhinitis
|
2.0%
1/50
The same event may appear as both an AE and a SAE. However, what is presented are distinct events. An event may be categorized as serious in one subject and as nonserious in another subject, or one subject may have experienced both a serious and nonserious event during the study.
|
0.00%
0/16
The same event may appear as both an AE and a SAE. However, what is presented are distinct events. An event may be categorized as serious in one subject and as nonserious in another subject, or one subject may have experienced both a serious and nonserious event during the study.
|
|
Infections and infestations
Sepsis
|
2.0%
1/50
The same event may appear as both an AE and a SAE. However, what is presented are distinct events. An event may be categorized as serious in one subject and as nonserious in another subject, or one subject may have experienced both a serious and nonserious event during the study.
|
0.00%
0/16
The same event may appear as both an AE and a SAE. However, what is presented are distinct events. An event may be categorized as serious in one subject and as nonserious in another subject, or one subject may have experienced both a serious and nonserious event during the study.
|
|
Infections and infestations
Skin candida
|
2.0%
1/50
The same event may appear as both an AE and a SAE. However, what is presented are distinct events. An event may be categorized as serious in one subject and as nonserious in another subject, or one subject may have experienced both a serious and nonserious event during the study.
|
0.00%
0/16
The same event may appear as both an AE and a SAE. However, what is presented are distinct events. An event may be categorized as serious in one subject and as nonserious in another subject, or one subject may have experienced both a serious and nonserious event during the study.
|
|
Infections and infestations
Skin infection
|
2.0%
1/50
The same event may appear as both an AE and a SAE. However, what is presented are distinct events. An event may be categorized as serious in one subject and as nonserious in another subject, or one subject may have experienced both a serious and nonserious event during the study.
|
0.00%
0/16
The same event may appear as both an AE and a SAE. However, what is presented are distinct events. An event may be categorized as serious in one subject and as nonserious in another subject, or one subject may have experienced both a serious and nonserious event during the study.
|
|
Infections and infestations
Staphylococcal skin infection
|
2.0%
1/50
The same event may appear as both an AE and a SAE. However, what is presented are distinct events. An event may be categorized as serious in one subject and as nonserious in another subject, or one subject may have experienced both a serious and nonserious event during the study.
|
0.00%
0/16
The same event may appear as both an AE and a SAE. However, what is presented are distinct events. An event may be categorized as serious in one subject and as nonserious in another subject, or one subject may have experienced both a serious and nonserious event during the study.
|
|
Infections and infestations
Upper respiratory tract infection
|
12.0%
6/50
The same event may appear as both an AE and a SAE. However, what is presented are distinct events. An event may be categorized as serious in one subject and as nonserious in another subject, or one subject may have experienced both a serious and nonserious event during the study.
|
6.2%
1/16
The same event may appear as both an AE and a SAE. However, what is presented are distinct events. An event may be categorized as serious in one subject and as nonserious in another subject, or one subject may have experienced both a serious and nonserious event during the study.
|
|
Infections and infestations
Urinary tract infection
|
8.0%
4/50
The same event may appear as both an AE and a SAE. However, what is presented are distinct events. An event may be categorized as serious in one subject and as nonserious in another subject, or one subject may have experienced both a serious and nonserious event during the study.
|
0.00%
0/16
The same event may appear as both an AE and a SAE. However, what is presented are distinct events. An event may be categorized as serious in one subject and as nonserious in another subject, or one subject may have experienced both a serious and nonserious event during the study.
|
|
Infections and infestations
Vulvovaginal mycotic infection
|
2.0%
1/50
The same event may appear as both an AE and a SAE. However, what is presented are distinct events. An event may be categorized as serious in one subject and as nonserious in another subject, or one subject may have experienced both a serious and nonserious event during the study.
|
0.00%
0/16
The same event may appear as both an AE and a SAE. However, what is presented are distinct events. An event may be categorized as serious in one subject and as nonserious in another subject, or one subject may have experienced both a serious and nonserious event during the study.
|
|
Injury, poisoning and procedural complications
Contusion
|
2.0%
1/50
The same event may appear as both an AE and a SAE. However, what is presented are distinct events. An event may be categorized as serious in one subject and as nonserious in another subject, or one subject may have experienced both a serious and nonserious event during the study.
|
0.00%
0/16
The same event may appear as both an AE and a SAE. However, what is presented are distinct events. An event may be categorized as serious in one subject and as nonserious in another subject, or one subject may have experienced both a serious and nonserious event during the study.
|
|
Injury, poisoning and procedural complications
Thermal burn
|
0.00%
0/50
The same event may appear as both an AE and a SAE. However, what is presented are distinct events. An event may be categorized as serious in one subject and as nonserious in another subject, or one subject may have experienced both a serious and nonserious event during the study.
|
6.2%
1/16
The same event may appear as both an AE and a SAE. However, what is presented are distinct events. An event may be categorized as serious in one subject and as nonserious in another subject, or one subject may have experienced both a serious and nonserious event during the study.
|
|
Investigations
Activated partial thromboplastin time
|
2.0%
1/50
The same event may appear as both an AE and a SAE. However, what is presented are distinct events. An event may be categorized as serious in one subject and as nonserious in another subject, or one subject may have experienced both a serious and nonserious event during the study.
|
0.00%
0/16
The same event may appear as both an AE and a SAE. However, what is presented are distinct events. An event may be categorized as serious in one subject and as nonserious in another subject, or one subject may have experienced both a serious and nonserious event during the study.
|
|
Investigations
Activated partial thromboplastin time prolonged
|
0.00%
0/50
The same event may appear as both an AE and a SAE. However, what is presented are distinct events. An event may be categorized as serious in one subject and as nonserious in another subject, or one subject may have experienced both a serious and nonserious event during the study.
|
6.2%
1/16
The same event may appear as both an AE and a SAE. However, what is presented are distinct events. An event may be categorized as serious in one subject and as nonserious in another subject, or one subject may have experienced both a serious and nonserious event during the study.
|
|
Investigations
Alanine aminotransferase increased
|
6.0%
3/50
The same event may appear as both an AE and a SAE. However, what is presented are distinct events. An event may be categorized as serious in one subject and as nonserious in another subject, or one subject may have experienced both a serious and nonserious event during the study.
|
0.00%
0/16
The same event may appear as both an AE and a SAE. However, what is presented are distinct events. An event may be categorized as serious in one subject and as nonserious in another subject, or one subject may have experienced both a serious and nonserious event during the study.
|
|
Investigations
Aspartate aminotransferase increased
|
12.0%
6/50
The same event may appear as both an AE and a SAE. However, what is presented are distinct events. An event may be categorized as serious in one subject and as nonserious in another subject, or one subject may have experienced both a serious and nonserious event during the study.
|
18.8%
3/16
The same event may appear as both an AE and a SAE. However, what is presented are distinct events. An event may be categorized as serious in one subject and as nonserious in another subject, or one subject may have experienced both a serious and nonserious event during the study.
|
|
Investigations
Blood alkaline phosphatase increased
|
8.0%
4/50
The same event may appear as both an AE and a SAE. However, what is presented are distinct events. An event may be categorized as serious in one subject and as nonserious in another subject, or one subject may have experienced both a serious and nonserious event during the study.
|
6.2%
1/16
The same event may appear as both an AE and a SAE. However, what is presented are distinct events. An event may be categorized as serious in one subject and as nonserious in another subject, or one subject may have experienced both a serious and nonserious event during the study.
|
|
Investigations
Blood bicarbonate
|
2.0%
1/50
The same event may appear as both an AE and a SAE. However, what is presented are distinct events. An event may be categorized as serious in one subject and as nonserious in another subject, or one subject may have experienced both a serious and nonserious event during the study.
|
0.00%
0/16
The same event may appear as both an AE and a SAE. However, what is presented are distinct events. An event may be categorized as serious in one subject and as nonserious in another subject, or one subject may have experienced both a serious and nonserious event during the study.
|
|
Investigations
Blood creatinine
|
4.0%
2/50
The same event may appear as both an AE and a SAE. However, what is presented are distinct events. An event may be categorized as serious in one subject and as nonserious in another subject, or one subject may have experienced both a serious and nonserious event during the study.
|
6.2%
1/16
The same event may appear as both an AE and a SAE. However, what is presented are distinct events. An event may be categorized as serious in one subject and as nonserious in another subject, or one subject may have experienced both a serious and nonserious event during the study.
|
|
Investigations
Haemoglobin decreased
|
4.0%
2/50
The same event may appear as both an AE and a SAE. However, what is presented are distinct events. An event may be categorized as serious in one subject and as nonserious in another subject, or one subject may have experienced both a serious and nonserious event during the study.
|
6.2%
1/16
The same event may appear as both an AE and a SAE. However, what is presented are distinct events. An event may be categorized as serious in one subject and as nonserious in another subject, or one subject may have experienced both a serious and nonserious event during the study.
|
|
Investigations
International normalised ratio
|
2.0%
1/50
The same event may appear as both an AE and a SAE. However, what is presented are distinct events. An event may be categorized as serious in one subject and as nonserious in another subject, or one subject may have experienced both a serious and nonserious event during the study.
|
0.00%
0/16
The same event may appear as both an AE and a SAE. However, what is presented are distinct events. An event may be categorized as serious in one subject and as nonserious in another subject, or one subject may have experienced both a serious and nonserious event during the study.
|
|
Investigations
International normalised ratio increased
|
0.00%
0/50
The same event may appear as both an AE and a SAE. However, what is presented are distinct events. An event may be categorized as serious in one subject and as nonserious in another subject, or one subject may have experienced both a serious and nonserious event during the study.
|
6.2%
1/16
The same event may appear as both an AE and a SAE. However, what is presented are distinct events. An event may be categorized as serious in one subject and as nonserious in another subject, or one subject may have experienced both a serious and nonserious event during the study.
|
|
Investigations
Urine leukocyte esterase positive
|
0.00%
0/50
The same event may appear as both an AE and a SAE. However, what is presented are distinct events. An event may be categorized as serious in one subject and as nonserious in another subject, or one subject may have experienced both a serious and nonserious event during the study.
|
6.2%
1/16
The same event may appear as both an AE and a SAE. However, what is presented are distinct events. An event may be categorized as serious in one subject and as nonserious in another subject, or one subject may have experienced both a serious and nonserious event during the study.
|
|
Investigations
Weight decreased
|
14.0%
7/50
The same event may appear as both an AE and a SAE. However, what is presented are distinct events. An event may be categorized as serious in one subject and as nonserious in another subject, or one subject may have experienced both a serious and nonserious event during the study.
|
18.8%
3/16
The same event may appear as both an AE and a SAE. However, what is presented are distinct events. An event may be categorized as serious in one subject and as nonserious in another subject, or one subject may have experienced both a serious and nonserious event during the study.
|
|
Metabolism and nutrition disorders
Acidosis
|
2.0%
1/50
The same event may appear as both an AE and a SAE. However, what is presented are distinct events. An event may be categorized as serious in one subject and as nonserious in another subject, or one subject may have experienced both a serious and nonserious event during the study.
|
0.00%
0/16
The same event may appear as both an AE and a SAE. However, what is presented are distinct events. An event may be categorized as serious in one subject and as nonserious in another subject, or one subject may have experienced both a serious and nonserious event during the study.
|
|
Metabolism and nutrition disorders
Decreased appetite
|
30.0%
15/50
The same event may appear as both an AE and a SAE. However, what is presented are distinct events. An event may be categorized as serious in one subject and as nonserious in another subject, or one subject may have experienced both a serious and nonserious event during the study.
|
37.5%
6/16
The same event may appear as both an AE and a SAE. However, what is presented are distinct events. An event may be categorized as serious in one subject and as nonserious in another subject, or one subject may have experienced both a serious and nonserious event during the study.
|
|
Metabolism and nutrition disorders
Dehydration
|
4.0%
2/50
The same event may appear as both an AE and a SAE. However, what is presented are distinct events. An event may be categorized as serious in one subject and as nonserious in another subject, or one subject may have experienced both a serious and nonserious event during the study.
|
0.00%
0/16
The same event may appear as both an AE and a SAE. However, what is presented are distinct events. An event may be categorized as serious in one subject and as nonserious in another subject, or one subject may have experienced both a serious and nonserious event during the study.
|
|
Metabolism and nutrition disorders
Hyperglycaemia
|
4.0%
2/50
The same event may appear as both an AE and a SAE. However, what is presented are distinct events. An event may be categorized as serious in one subject and as nonserious in another subject, or one subject may have experienced both a serious and nonserious event during the study.
|
6.2%
1/16
The same event may appear as both an AE and a SAE. However, what is presented are distinct events. An event may be categorized as serious in one subject and as nonserious in another subject, or one subject may have experienced both a serious and nonserious event during the study.
|
|
Metabolism and nutrition disorders
Hyperkalaemia
|
4.0%
2/50
The same event may appear as both an AE and a SAE. However, what is presented are distinct events. An event may be categorized as serious in one subject and as nonserious in another subject, or one subject may have experienced both a serious and nonserious event during the study.
|
0.00%
0/16
The same event may appear as both an AE and a SAE. However, what is presented are distinct events. An event may be categorized as serious in one subject and as nonserious in another subject, or one subject may have experienced both a serious and nonserious event during the study.
|
|
Metabolism and nutrition disorders
Hypernatraemia
|
2.0%
1/50
The same event may appear as both an AE and a SAE. However, what is presented are distinct events. An event may be categorized as serious in one subject and as nonserious in another subject, or one subject may have experienced both a serious and nonserious event during the study.
|
0.00%
0/16
The same event may appear as both an AE and a SAE. However, what is presented are distinct events. An event may be categorized as serious in one subject and as nonserious in another subject, or one subject may have experienced both a serious and nonserious event during the study.
|
|
Metabolism and nutrition disorders
Hypoalbuminaemia
|
10.0%
5/50
The same event may appear as both an AE and a SAE. However, what is presented are distinct events. An event may be categorized as serious in one subject and as nonserious in another subject, or one subject may have experienced both a serious and nonserious event during the study.
|
18.8%
3/16
The same event may appear as both an AE and a SAE. However, what is presented are distinct events. An event may be categorized as serious in one subject and as nonserious in another subject, or one subject may have experienced both a serious and nonserious event during the study.
|
|
Metabolism and nutrition disorders
Hypocalcaemia
|
8.0%
4/50
The same event may appear as both an AE and a SAE. However, what is presented are distinct events. An event may be categorized as serious in one subject and as nonserious in another subject, or one subject may have experienced both a serious and nonserious event during the study.
|
6.2%
1/16
The same event may appear as both an AE and a SAE. However, what is presented are distinct events. An event may be categorized as serious in one subject and as nonserious in another subject, or one subject may have experienced both a serious and nonserious event during the study.
|
|
Metabolism and nutrition disorders
Hypoglycaemia
|
2.0%
1/50
The same event may appear as both an AE and a SAE. However, what is presented are distinct events. An event may be categorized as serious in one subject and as nonserious in another subject, or one subject may have experienced both a serious and nonserious event during the study.
|
6.2%
1/16
The same event may appear as both an AE and a SAE. However, what is presented are distinct events. An event may be categorized as serious in one subject and as nonserious in another subject, or one subject may have experienced both a serious and nonserious event during the study.
|
|
Metabolism and nutrition disorders
Hypokalaemia
|
6.0%
3/50
The same event may appear as both an AE and a SAE. However, what is presented are distinct events. An event may be categorized as serious in one subject and as nonserious in another subject, or one subject may have experienced both a serious and nonserious event during the study.
|
6.2%
1/16
The same event may appear as both an AE and a SAE. However, what is presented are distinct events. An event may be categorized as serious in one subject and as nonserious in another subject, or one subject may have experienced both a serious and nonserious event during the study.
|
|
Metabolism and nutrition disorders
Hypomagnesaemia
|
10.0%
5/50
The same event may appear as both an AE and a SAE. However, what is presented are distinct events. An event may be categorized as serious in one subject and as nonserious in another subject, or one subject may have experienced both a serious and nonserious event during the study.
|
0.00%
0/16
The same event may appear as both an AE and a SAE. However, what is presented are distinct events. An event may be categorized as serious in one subject and as nonserious in another subject, or one subject may have experienced both a serious and nonserious event during the study.
|
|
Metabolism and nutrition disorders
Hyponatraemia
|
0.00%
0/50
The same event may appear as both an AE and a SAE. However, what is presented are distinct events. An event may be categorized as serious in one subject and as nonserious in another subject, or one subject may have experienced both a serious and nonserious event during the study.
|
6.2%
1/16
The same event may appear as both an AE and a SAE. However, what is presented are distinct events. An event may be categorized as serious in one subject and as nonserious in another subject, or one subject may have experienced both a serious and nonserious event during the study.
|
|
Metabolism and nutrition disorders
Hypophosphataemia
|
6.0%
3/50
The same event may appear as both an AE and a SAE. However, what is presented are distinct events. An event may be categorized as serious in one subject and as nonserious in another subject, or one subject may have experienced both a serious and nonserious event during the study.
|
6.2%
1/16
The same event may appear as both an AE and a SAE. However, what is presented are distinct events. An event may be categorized as serious in one subject and as nonserious in another subject, or one subject may have experienced both a serious and nonserious event during the study.
|
|
Musculoskeletal and connective tissue disorders
Arthralgia
|
4.0%
2/50
The same event may appear as both an AE and a SAE. However, what is presented are distinct events. An event may be categorized as serious in one subject and as nonserious in another subject, or one subject may have experienced both a serious and nonserious event during the study.
|
12.5%
2/16
The same event may appear as both an AE and a SAE. However, what is presented are distinct events. An event may be categorized as serious in one subject and as nonserious in another subject, or one subject may have experienced both a serious and nonserious event during the study.
|
|
Musculoskeletal and connective tissue disorders
Back pain
|
10.0%
5/50
The same event may appear as both an AE and a SAE. However, what is presented are distinct events. An event may be categorized as serious in one subject and as nonserious in another subject, or one subject may have experienced both a serious and nonserious event during the study.
|
6.2%
1/16
The same event may appear as both an AE and a SAE. However, what is presented are distinct events. An event may be categorized as serious in one subject and as nonserious in another subject, or one subject may have experienced both a serious and nonserious event during the study.
|
|
Musculoskeletal and connective tissue disorders
Bone pain
|
4.0%
2/50
The same event may appear as both an AE and a SAE. However, what is presented are distinct events. An event may be categorized as serious in one subject and as nonserious in another subject, or one subject may have experienced both a serious and nonserious event during the study.
|
0.00%
0/16
The same event may appear as both an AE and a SAE. However, what is presented are distinct events. An event may be categorized as serious in one subject and as nonserious in another subject, or one subject may have experienced both a serious and nonserious event during the study.
|
|
Musculoskeletal and connective tissue disorders
Coccydynia
|
2.0%
1/50
The same event may appear as both an AE and a SAE. However, what is presented are distinct events. An event may be categorized as serious in one subject and as nonserious in another subject, or one subject may have experienced both a serious and nonserious event during the study.
|
0.00%
0/16
The same event may appear as both an AE and a SAE. However, what is presented are distinct events. An event may be categorized as serious in one subject and as nonserious in another subject, or one subject may have experienced both a serious and nonserious event during the study.
|
|
Musculoskeletal and connective tissue disorders
Flank pain
|
2.0%
1/50
The same event may appear as both an AE and a SAE. However, what is presented are distinct events. An event may be categorized as serious in one subject and as nonserious in another subject, or one subject may have experienced both a serious and nonserious event during the study.
|
0.00%
0/16
The same event may appear as both an AE and a SAE. However, what is presented are distinct events. An event may be categorized as serious in one subject and as nonserious in another subject, or one subject may have experienced both a serious and nonserious event during the study.
|
|
Musculoskeletal and connective tissue disorders
Groin pain
|
0.00%
0/50
The same event may appear as both an AE and a SAE. However, what is presented are distinct events. An event may be categorized as serious in one subject and as nonserious in another subject, or one subject may have experienced both a serious and nonserious event during the study.
|
6.2%
1/16
The same event may appear as both an AE and a SAE. However, what is presented are distinct events. An event may be categorized as serious in one subject and as nonserious in another subject, or one subject may have experienced both a serious and nonserious event during the study.
|
|
Musculoskeletal and connective tissue disorders
Muscle spasms
|
12.0%
6/50
The same event may appear as both an AE and a SAE. However, what is presented are distinct events. An event may be categorized as serious in one subject and as nonserious in another subject, or one subject may have experienced both a serious and nonserious event during the study.
|
0.00%
0/16
The same event may appear as both an AE and a SAE. However, what is presented are distinct events. An event may be categorized as serious in one subject and as nonserious in another subject, or one subject may have experienced both a serious and nonserious event during the study.
|
|
Musculoskeletal and connective tissue disorders
Muscle twitching
|
2.0%
1/50
The same event may appear as both an AE and a SAE. However, what is presented are distinct events. An event may be categorized as serious in one subject and as nonserious in another subject, or one subject may have experienced both a serious and nonserious event during the study.
|
0.00%
0/16
The same event may appear as both an AE and a SAE. However, what is presented are distinct events. An event may be categorized as serious in one subject and as nonserious in another subject, or one subject may have experienced both a serious and nonserious event during the study.
|
|
Musculoskeletal and connective tissue disorders
Musculoskeletal chest pain
|
6.0%
3/50
The same event may appear as both an AE and a SAE. However, what is presented are distinct events. An event may be categorized as serious in one subject and as nonserious in another subject, or one subject may have experienced both a serious and nonserious event during the study.
|
0.00%
0/16
The same event may appear as both an AE and a SAE. However, what is presented are distinct events. An event may be categorized as serious in one subject and as nonserious in another subject, or one subject may have experienced both a serious and nonserious event during the study.
|
|
Musculoskeletal and connective tissue disorders
Musculoskeletal pain
|
2.0%
1/50
The same event may appear as both an AE and a SAE. However, what is presented are distinct events. An event may be categorized as serious in one subject and as nonserious in another subject, or one subject may have experienced both a serious and nonserious event during the study.
|
6.2%
1/16
The same event may appear as both an AE and a SAE. However, what is presented are distinct events. An event may be categorized as serious in one subject and as nonserious in another subject, or one subject may have experienced both a serious and nonserious event during the study.
|
|
Musculoskeletal and connective tissue disorders
Myalgia
|
2.0%
1/50
The same event may appear as both an AE and a SAE. However, what is presented are distinct events. An event may be categorized as serious in one subject and as nonserious in another subject, or one subject may have experienced both a serious and nonserious event during the study.
|
0.00%
0/16
The same event may appear as both an AE and a SAE. However, what is presented are distinct events. An event may be categorized as serious in one subject and as nonserious in another subject, or one subject may have experienced both a serious and nonserious event during the study.
|
|
Musculoskeletal and connective tissue disorders
Pain in extremity
|
2.0%
1/50
The same event may appear as both an AE and a SAE. However, what is presented are distinct events. An event may be categorized as serious in one subject and as nonserious in another subject, or one subject may have experienced both a serious and nonserious event during the study.
|
0.00%
0/16
The same event may appear as both an AE and a SAE. However, what is presented are distinct events. An event may be categorized as serious in one subject and as nonserious in another subject, or one subject may have experienced both a serious and nonserious event during the study.
|
|
Neoplasms benign, malignant and unspecified (incl cysts and polyps)
Metastatic pain
|
2.0%
1/50
The same event may appear as both an AE and a SAE. However, what is presented are distinct events. An event may be categorized as serious in one subject and as nonserious in another subject, or one subject may have experienced both a serious and nonserious event during the study.
|
0.00%
0/16
The same event may appear as both an AE and a SAE. However, what is presented are distinct events. An event may be categorized as serious in one subject and as nonserious in another subject, or one subject may have experienced both a serious and nonserious event during the study.
|
|
Neoplasms benign, malignant and unspecified (incl cysts and polyps)
Tumour haemorrhage
|
0.00%
0/50
The same event may appear as both an AE and a SAE. However, what is presented are distinct events. An event may be categorized as serious in one subject and as nonserious in another subject, or one subject may have experienced both a serious and nonserious event during the study.
|
6.2%
1/16
The same event may appear as both an AE and a SAE. However, what is presented are distinct events. An event may be categorized as serious in one subject and as nonserious in another subject, or one subject may have experienced both a serious and nonserious event during the study.
|
|
Nervous system disorders
Ataxia
|
0.00%
0/50
The same event may appear as both an AE and a SAE. However, what is presented are distinct events. An event may be categorized as serious in one subject and as nonserious in another subject, or one subject may have experienced both a serious and nonserious event during the study.
|
6.2%
1/16
The same event may appear as both an AE and a SAE. However, what is presented are distinct events. An event may be categorized as serious in one subject and as nonserious in another subject, or one subject may have experienced both a serious and nonserious event during the study.
|
|
Nervous system disorders
Balance disorder
|
0.00%
0/50
The same event may appear as both an AE and a SAE. However, what is presented are distinct events. An event may be categorized as serious in one subject and as nonserious in another subject, or one subject may have experienced both a serious and nonserious event during the study.
|
6.2%
1/16
The same event may appear as both an AE and a SAE. However, what is presented are distinct events. An event may be categorized as serious in one subject and as nonserious in another subject, or one subject may have experienced both a serious and nonserious event during the study.
|
|
Nervous system disorders
Dizziness
|
0.00%
0/50
The same event may appear as both an AE and a SAE. However, what is presented are distinct events. An event may be categorized as serious in one subject and as nonserious in another subject, or one subject may have experienced both a serious and nonserious event during the study.
|
12.5%
2/16
The same event may appear as both an AE and a SAE. However, what is presented are distinct events. An event may be categorized as serious in one subject and as nonserious in another subject, or one subject may have experienced both a serious and nonserious event during the study.
|
|
Nervous system disorders
Dysgeusia
|
8.0%
4/50
The same event may appear as both an AE and a SAE. However, what is presented are distinct events. An event may be categorized as serious in one subject and as nonserious in another subject, or one subject may have experienced both a serious and nonserious event during the study.
|
6.2%
1/16
The same event may appear as both an AE and a SAE. However, what is presented are distinct events. An event may be categorized as serious in one subject and as nonserious in another subject, or one subject may have experienced both a serious and nonserious event during the study.
|
|
Nervous system disorders
Headache
|
2.0%
1/50
The same event may appear as both an AE and a SAE. However, what is presented are distinct events. An event may be categorized as serious in one subject and as nonserious in another subject, or one subject may have experienced both a serious and nonserious event during the study.
|
12.5%
2/16
The same event may appear as both an AE and a SAE. However, what is presented are distinct events. An event may be categorized as serious in one subject and as nonserious in another subject, or one subject may have experienced both a serious and nonserious event during the study.
|
|
Nervous system disorders
Hypoaesthesia
|
4.0%
2/50
The same event may appear as both an AE and a SAE. However, what is presented are distinct events. An event may be categorized as serious in one subject and as nonserious in another subject, or one subject may have experienced both a serious and nonserious event during the study.
|
0.00%
0/16
The same event may appear as both an AE and a SAE. However, what is presented are distinct events. An event may be categorized as serious in one subject and as nonserious in another subject, or one subject may have experienced both a serious and nonserious event during the study.
|
|
Nervous system disorders
Memory impairment
|
0.00%
0/50
The same event may appear as both an AE and a SAE. However, what is presented are distinct events. An event may be categorized as serious in one subject and as nonserious in another subject, or one subject may have experienced both a serious and nonserious event during the study.
|
12.5%
2/16
The same event may appear as both an AE and a SAE. However, what is presented are distinct events. An event may be categorized as serious in one subject and as nonserious in another subject, or one subject may have experienced both a serious and nonserious event during the study.
|
|
Nervous system disorders
Paraesthesia
|
2.0%
1/50
The same event may appear as both an AE and a SAE. However, what is presented are distinct events. An event may be categorized as serious in one subject and as nonserious in another subject, or one subject may have experienced both a serious and nonserious event during the study.
|
0.00%
0/16
The same event may appear as both an AE and a SAE. However, what is presented are distinct events. An event may be categorized as serious in one subject and as nonserious in another subject, or one subject may have experienced both a serious and nonserious event during the study.
|
|
Nervous system disorders
Partial seizures
|
2.0%
1/50
The same event may appear as both an AE and a SAE. However, what is presented are distinct events. An event may be categorized as serious in one subject and as nonserious in another subject, or one subject may have experienced both a serious and nonserious event during the study.
|
0.00%
0/16
The same event may appear as both an AE and a SAE. However, what is presented are distinct events. An event may be categorized as serious in one subject and as nonserious in another subject, or one subject may have experienced both a serious and nonserious event during the study.
|
|
Nervous system disorders
Peripheral sensory neuropathy
|
4.0%
2/50
The same event may appear as both an AE and a SAE. However, what is presented are distinct events. An event may be categorized as serious in one subject and as nonserious in another subject, or one subject may have experienced both a serious and nonserious event during the study.
|
0.00%
0/16
The same event may appear as both an AE and a SAE. However, what is presented are distinct events. An event may be categorized as serious in one subject and as nonserious in another subject, or one subject may have experienced both a serious and nonserious event during the study.
|
|
Nervous system disorders
Psychomotor hyperactivity
|
2.0%
1/50
The same event may appear as both an AE and a SAE. However, what is presented are distinct events. An event may be categorized as serious in one subject and as nonserious in another subject, or one subject may have experienced both a serious and nonserious event during the study.
|
0.00%
0/16
The same event may appear as both an AE and a SAE. However, what is presented are distinct events. An event may be categorized as serious in one subject and as nonserious in another subject, or one subject may have experienced both a serious and nonserious event during the study.
|
|
Nervous system disorders
Tremor
|
2.0%
1/50
The same event may appear as both an AE and a SAE. However, what is presented are distinct events. An event may be categorized as serious in one subject and as nonserious in another subject, or one subject may have experienced both a serious and nonserious event during the study.
|
0.00%
0/16
The same event may appear as both an AE and a SAE. However, what is presented are distinct events. An event may be categorized as serious in one subject and as nonserious in another subject, or one subject may have experienced both a serious and nonserious event during the study.
|
|
Psychiatric disorders
Anxiety
|
0.00%
0/50
The same event may appear as both an AE and a SAE. However, what is presented are distinct events. An event may be categorized as serious in one subject and as nonserious in another subject, or one subject may have experienced both a serious and nonserious event during the study.
|
6.2%
1/16
The same event may appear as both an AE and a SAE. However, what is presented are distinct events. An event may be categorized as serious in one subject and as nonserious in another subject, or one subject may have experienced both a serious and nonserious event during the study.
|
|
Psychiatric disorders
Depression
|
4.0%
2/50
The same event may appear as both an AE and a SAE. However, what is presented are distinct events. An event may be categorized as serious in one subject and as nonserious in another subject, or one subject may have experienced both a serious and nonserious event during the study.
|
0.00%
0/16
The same event may appear as both an AE and a SAE. However, what is presented are distinct events. An event may be categorized as serious in one subject and as nonserious in another subject, or one subject may have experienced both a serious and nonserious event during the study.
|
|
Psychiatric disorders
Insomnia
|
4.0%
2/50
The same event may appear as both an AE and a SAE. However, what is presented are distinct events. An event may be categorized as serious in one subject and as nonserious in another subject, or one subject may have experienced both a serious and nonserious event during the study.
|
6.2%
1/16
The same event may appear as both an AE and a SAE. However, what is presented are distinct events. An event may be categorized as serious in one subject and as nonserious in another subject, or one subject may have experienced both a serious and nonserious event during the study.
|
|
Psychiatric disorders
Mental status changes
|
2.0%
1/50
The same event may appear as both an AE and a SAE. However, what is presented are distinct events. An event may be categorized as serious in one subject and as nonserious in another subject, or one subject may have experienced both a serious and nonserious event during the study.
|
0.00%
0/16
The same event may appear as both an AE and a SAE. However, what is presented are distinct events. An event may be categorized as serious in one subject and as nonserious in another subject, or one subject may have experienced both a serious and nonserious event during the study.
|
|
Psychiatric disorders
Reading disorder
|
0.00%
0/50
The same event may appear as both an AE and a SAE. However, what is presented are distinct events. An event may be categorized as serious in one subject and as nonserious in another subject, or one subject may have experienced both a serious and nonserious event during the study.
|
6.2%
1/16
The same event may appear as both an AE and a SAE. However, what is presented are distinct events. An event may be categorized as serious in one subject and as nonserious in another subject, or one subject may have experienced both a serious and nonserious event during the study.
|
|
Renal and urinary disorders
Dysuria
|
0.00%
0/50
The same event may appear as both an AE and a SAE. However, what is presented are distinct events. An event may be categorized as serious in one subject and as nonserious in another subject, or one subject may have experienced both a serious and nonserious event during the study.
|
6.2%
1/16
The same event may appear as both an AE and a SAE. However, what is presented are distinct events. An event may be categorized as serious in one subject and as nonserious in another subject, or one subject may have experienced both a serious and nonserious event during the study.
|
|
Renal and urinary disorders
Micturition urgency
|
0.00%
0/50
The same event may appear as both an AE and a SAE. However, what is presented are distinct events. An event may be categorized as serious in one subject and as nonserious in another subject, or one subject may have experienced both a serious and nonserious event during the study.
|
6.2%
1/16
The same event may appear as both an AE and a SAE. However, what is presented are distinct events. An event may be categorized as serious in one subject and as nonserious in another subject, or one subject may have experienced both a serious and nonserious event during the study.
|
|
Renal and urinary disorders
Pollakiuria
|
0.00%
0/50
The same event may appear as both an AE and a SAE. However, what is presented are distinct events. An event may be categorized as serious in one subject and as nonserious in another subject, or one subject may have experienced both a serious and nonserious event during the study.
|
6.2%
1/16
The same event may appear as both an AE and a SAE. However, what is presented are distinct events. An event may be categorized as serious in one subject and as nonserious in another subject, or one subject may have experienced both a serious and nonserious event during the study.
|
|
Renal and urinary disorders
Proteinuria
|
2.0%
1/50
The same event may appear as both an AE and a SAE. However, what is presented are distinct events. An event may be categorized as serious in one subject and as nonserious in another subject, or one subject may have experienced both a serious and nonserious event during the study.
|
0.00%
0/16
The same event may appear as both an AE and a SAE. However, what is presented are distinct events. An event may be categorized as serious in one subject and as nonserious in another subject, or one subject may have experienced both a serious and nonserious event during the study.
|
|
Renal and urinary disorders
Renal failure
|
2.0%
1/50
The same event may appear as both an AE and a SAE. However, what is presented are distinct events. An event may be categorized as serious in one subject and as nonserious in another subject, or one subject may have experienced both a serious and nonserious event during the study.
|
0.00%
0/16
The same event may appear as both an AE and a SAE. However, what is presented are distinct events. An event may be categorized as serious in one subject and as nonserious in another subject, or one subject may have experienced both a serious and nonserious event during the study.
|
|
Renal and urinary disorders
Urinary retention
|
0.00%
0/50
The same event may appear as both an AE and a SAE. However, what is presented are distinct events. An event may be categorized as serious in one subject and as nonserious in another subject, or one subject may have experienced both a serious and nonserious event during the study.
|
6.2%
1/16
The same event may appear as both an AE and a SAE. However, what is presented are distinct events. An event may be categorized as serious in one subject and as nonserious in another subject, or one subject may have experienced both a serious and nonserious event during the study.
|
|
Reproductive system and breast disorders
Vulvovaginal dryness
|
6.0%
3/50
The same event may appear as both an AE and a SAE. However, what is presented are distinct events. An event may be categorized as serious in one subject and as nonserious in another subject, or one subject may have experienced both a serious and nonserious event during the study.
|
0.00%
0/16
The same event may appear as both an AE and a SAE. However, what is presented are distinct events. An event may be categorized as serious in one subject and as nonserious in another subject, or one subject may have experienced both a serious and nonserious event during the study.
|
|
Reproductive system and breast disorders
Vulvovaginal pruritus
|
2.0%
1/50
The same event may appear as both an AE and a SAE. However, what is presented are distinct events. An event may be categorized as serious in one subject and as nonserious in another subject, or one subject may have experienced both a serious and nonserious event during the study.
|
0.00%
0/16
The same event may appear as both an AE and a SAE. However, what is presented are distinct events. An event may be categorized as serious in one subject and as nonserious in another subject, or one subject may have experienced both a serious and nonserious event during the study.
|
|
Respiratory, thoracic and mediastinal disorders
Cough
|
12.0%
6/50
The same event may appear as both an AE and a SAE. However, what is presented are distinct events. An event may be categorized as serious in one subject and as nonserious in another subject, or one subject may have experienced both a serious and nonserious event during the study.
|
6.2%
1/16
The same event may appear as both an AE and a SAE. However, what is presented are distinct events. An event may be categorized as serious in one subject and as nonserious in another subject, or one subject may have experienced both a serious and nonserious event during the study.
|
|
Respiratory, thoracic and mediastinal disorders
Dyspnoea
|
14.0%
7/50
The same event may appear as both an AE and a SAE. However, what is presented are distinct events. An event may be categorized as serious in one subject and as nonserious in another subject, or one subject may have experienced both a serious and nonserious event during the study.
|
12.5%
2/16
The same event may appear as both an AE and a SAE. However, what is presented are distinct events. An event may be categorized as serious in one subject and as nonserious in another subject, or one subject may have experienced both a serious and nonserious event during the study.
|
|
Respiratory, thoracic and mediastinal disorders
Dyspnoea exertional
|
2.0%
1/50
The same event may appear as both an AE and a SAE. However, what is presented are distinct events. An event may be categorized as serious in one subject and as nonserious in another subject, or one subject may have experienced both a serious and nonserious event during the study.
|
0.00%
0/16
The same event may appear as both an AE and a SAE. However, what is presented are distinct events. An event may be categorized as serious in one subject and as nonserious in another subject, or one subject may have experienced both a serious and nonserious event during the study.
|
|
Respiratory, thoracic and mediastinal disorders
Epistaxis
|
8.0%
4/50
The same event may appear as both an AE and a SAE. However, what is presented are distinct events. An event may be categorized as serious in one subject and as nonserious in another subject, or one subject may have experienced both a serious and nonserious event during the study.
|
6.2%
1/16
The same event may appear as both an AE and a SAE. However, what is presented are distinct events. An event may be categorized as serious in one subject and as nonserious in another subject, or one subject may have experienced both a serious and nonserious event during the study.
|
|
Respiratory, thoracic and mediastinal disorders
Haemoptysis
|
2.0%
1/50
The same event may appear as both an AE and a SAE. However, what is presented are distinct events. An event may be categorized as serious in one subject and as nonserious in another subject, or one subject may have experienced both a serious and nonserious event during the study.
|
6.2%
1/16
The same event may appear as both an AE and a SAE. However, what is presented are distinct events. An event may be categorized as serious in one subject and as nonserious in another subject, or one subject may have experienced both a serious and nonserious event during the study.
|
|
Respiratory, thoracic and mediastinal disorders
Increased upper airway secretion
|
2.0%
1/50
The same event may appear as both an AE and a SAE. However, what is presented are distinct events. An event may be categorized as serious in one subject and as nonserious in another subject, or one subject may have experienced both a serious and nonserious event during the study.
|
0.00%
0/16
The same event may appear as both an AE and a SAE. However, what is presented are distinct events. An event may be categorized as serious in one subject and as nonserious in another subject, or one subject may have experienced both a serious and nonserious event during the study.
|
|
Respiratory, thoracic and mediastinal disorders
Nasal congestion
|
6.0%
3/50
The same event may appear as both an AE and a SAE. However, what is presented are distinct events. An event may be categorized as serious in one subject and as nonserious in another subject, or one subject may have experienced both a serious and nonserious event during the study.
|
0.00%
0/16
The same event may appear as both an AE and a SAE. However, what is presented are distinct events. An event may be categorized as serious in one subject and as nonserious in another subject, or one subject may have experienced both a serious and nonserious event during the study.
|
|
Respiratory, thoracic and mediastinal disorders
Nasal discomfort
|
2.0%
1/50
The same event may appear as both an AE and a SAE. However, what is presented are distinct events. An event may be categorized as serious in one subject and as nonserious in another subject, or one subject may have experienced both a serious and nonserious event during the study.
|
0.00%
0/16
The same event may appear as both an AE and a SAE. However, what is presented are distinct events. An event may be categorized as serious in one subject and as nonserious in another subject, or one subject may have experienced both a serious and nonserious event during the study.
|
|
Respiratory, thoracic and mediastinal disorders
Nasal dryness
|
6.0%
3/50
The same event may appear as both an AE and a SAE. However, what is presented are distinct events. An event may be categorized as serious in one subject and as nonserious in another subject, or one subject may have experienced both a serious and nonserious event during the study.
|
0.00%
0/16
The same event may appear as both an AE and a SAE. However, what is presented are distinct events. An event may be categorized as serious in one subject and as nonserious in another subject, or one subject may have experienced both a serious and nonserious event during the study.
|
|
Respiratory, thoracic and mediastinal disorders
Oropharyngeal pain
|
6.0%
3/50
The same event may appear as both an AE and a SAE. However, what is presented are distinct events. An event may be categorized as serious in one subject and as nonserious in another subject, or one subject may have experienced both a serious and nonserious event during the study.
|
0.00%
0/16
The same event may appear as both an AE and a SAE. However, what is presented are distinct events. An event may be categorized as serious in one subject and as nonserious in another subject, or one subject may have experienced both a serious and nonserious event during the study.
|
|
Respiratory, thoracic and mediastinal disorders
Pharyngeal ulceration
|
2.0%
1/50
The same event may appear as both an AE and a SAE. However, what is presented are distinct events. An event may be categorized as serious in one subject and as nonserious in another subject, or one subject may have experienced both a serious and nonserious event during the study.
|
0.00%
0/16
The same event may appear as both an AE and a SAE. However, what is presented are distinct events. An event may be categorized as serious in one subject and as nonserious in another subject, or one subject may have experienced both a serious and nonserious event during the study.
|
|
Respiratory, thoracic and mediastinal disorders
Productive cough
|
2.0%
1/50
The same event may appear as both an AE and a SAE. However, what is presented are distinct events. An event may be categorized as serious in one subject and as nonserious in another subject, or one subject may have experienced both a serious and nonserious event during the study.
|
6.2%
1/16
The same event may appear as both an AE and a SAE. However, what is presented are distinct events. An event may be categorized as serious in one subject and as nonserious in another subject, or one subject may have experienced both a serious and nonserious event during the study.
|
|
Respiratory, thoracic and mediastinal disorders
Pulmonary embolism
|
2.0%
1/50
The same event may appear as both an AE and a SAE. However, what is presented are distinct events. An event may be categorized as serious in one subject and as nonserious in another subject, or one subject may have experienced both a serious and nonserious event during the study.
|
0.00%
0/16
The same event may appear as both an AE and a SAE. However, what is presented are distinct events. An event may be categorized as serious in one subject and as nonserious in another subject, or one subject may have experienced both a serious and nonserious event during the study.
|
|
Respiratory, thoracic and mediastinal disorders
Respiratory tract congestion
|
2.0%
1/50
The same event may appear as both an AE and a SAE. However, what is presented are distinct events. An event may be categorized as serious in one subject and as nonserious in another subject, or one subject may have experienced both a serious and nonserious event during the study.
|
0.00%
0/16
The same event may appear as both an AE and a SAE. However, what is presented are distinct events. An event may be categorized as serious in one subject and as nonserious in another subject, or one subject may have experienced both a serious and nonserious event during the study.
|
|
Respiratory, thoracic and mediastinal disorders
Rhinitis allergic
|
6.0%
3/50
The same event may appear as both an AE and a SAE. However, what is presented are distinct events. An event may be categorized as serious in one subject and as nonserious in another subject, or one subject may have experienced both a serious and nonserious event during the study.
|
6.2%
1/16
The same event may appear as both an AE and a SAE. However, what is presented are distinct events. An event may be categorized as serious in one subject and as nonserious in another subject, or one subject may have experienced both a serious and nonserious event during the study.
|
|
Respiratory, thoracic and mediastinal disorders
Rhinorrhoea
|
2.0%
1/50
The same event may appear as both an AE and a SAE. However, what is presented are distinct events. An event may be categorized as serious in one subject and as nonserious in another subject, or one subject may have experienced both a serious and nonserious event during the study.
|
0.00%
0/16
The same event may appear as both an AE and a SAE. However, what is presented are distinct events. An event may be categorized as serious in one subject and as nonserious in another subject, or one subject may have experienced both a serious and nonserious event during the study.
|
|
Respiratory, thoracic and mediastinal disorders
Upper-airway cough syndrome
|
2.0%
1/50
The same event may appear as both an AE and a SAE. However, what is presented are distinct events. An event may be categorized as serious in one subject and as nonserious in another subject, or one subject may have experienced both a serious and nonserious event during the study.
|
0.00%
0/16
The same event may appear as both an AE and a SAE. However, what is presented are distinct events. An event may be categorized as serious in one subject and as nonserious in another subject, or one subject may have experienced both a serious and nonserious event during the study.
|
|
Respiratory, thoracic and mediastinal disorders
Wheezing
|
2.0%
1/50
The same event may appear as both an AE and a SAE. However, what is presented are distinct events. An event may be categorized as serious in one subject and as nonserious in another subject, or one subject may have experienced both a serious and nonserious event during the study.
|
0.00%
0/16
The same event may appear as both an AE and a SAE. However, what is presented are distinct events. An event may be categorized as serious in one subject and as nonserious in another subject, or one subject may have experienced both a serious and nonserious event during the study.
|
|
Skin and subcutaneous tissue disorders
Alopecia
|
4.0%
2/50
The same event may appear as both an AE and a SAE. However, what is presented are distinct events. An event may be categorized as serious in one subject and as nonserious in another subject, or one subject may have experienced both a serious and nonserious event during the study.
|
0.00%
0/16
The same event may appear as both an AE and a SAE. However, what is presented are distinct events. An event may be categorized as serious in one subject and as nonserious in another subject, or one subject may have experienced both a serious and nonserious event during the study.
|
|
Skin and subcutaneous tissue disorders
Dermatitis acneiform
|
66.0%
33/50
The same event may appear as both an AE and a SAE. However, what is presented are distinct events. An event may be categorized as serious in one subject and as nonserious in another subject, or one subject may have experienced both a serious and nonserious event during the study.
|
75.0%
12/16
The same event may appear as both an AE and a SAE. However, what is presented are distinct events. An event may be categorized as serious in one subject and as nonserious in another subject, or one subject may have experienced both a serious and nonserious event during the study.
|
|
Skin and subcutaneous tissue disorders
Dermatitis allergic
|
2.0%
1/50
The same event may appear as both an AE and a SAE. However, what is presented are distinct events. An event may be categorized as serious in one subject and as nonserious in another subject, or one subject may have experienced both a serious and nonserious event during the study.
|
0.00%
0/16
The same event may appear as both an AE and a SAE. However, what is presented are distinct events. An event may be categorized as serious in one subject and as nonserious in another subject, or one subject may have experienced both a serious and nonserious event during the study.
|
|
Skin and subcutaneous tissue disorders
Dry skin
|
36.0%
18/50
The same event may appear as both an AE and a SAE. However, what is presented are distinct events. An event may be categorized as serious in one subject and as nonserious in another subject, or one subject may have experienced both a serious and nonserious event during the study.
|
43.8%
7/16
The same event may appear as both an AE and a SAE. However, what is presented are distinct events. An event may be categorized as serious in one subject and as nonserious in another subject, or one subject may have experienced both a serious and nonserious event during the study.
|
|
Skin and subcutaneous tissue disorders
Erythema
|
10.0%
5/50
The same event may appear as both an AE and a SAE. However, what is presented are distinct events. An event may be categorized as serious in one subject and as nonserious in another subject, or one subject may have experienced both a serious and nonserious event during the study.
|
0.00%
0/16
The same event may appear as both an AE and a SAE. However, what is presented are distinct events. An event may be categorized as serious in one subject and as nonserious in another subject, or one subject may have experienced both a serious and nonserious event during the study.
|
|
Skin and subcutaneous tissue disorders
Erythema multiforme
|
2.0%
1/50
The same event may appear as both an AE and a SAE. However, what is presented are distinct events. An event may be categorized as serious in one subject and as nonserious in another subject, or one subject may have experienced both a serious and nonserious event during the study.
|
0.00%
0/16
The same event may appear as both an AE and a SAE. However, what is presented are distinct events. An event may be categorized as serious in one subject and as nonserious in another subject, or one subject may have experienced both a serious and nonserious event during the study.
|
|
Skin and subcutaneous tissue disorders
Exfoliative rash
|
24.0%
12/50
The same event may appear as both an AE and a SAE. However, what is presented are distinct events. An event may be categorized as serious in one subject and as nonserious in another subject, or one subject may have experienced both a serious and nonserious event during the study.
|
25.0%
4/16
The same event may appear as both an AE and a SAE. However, what is presented are distinct events. An event may be categorized as serious in one subject and as nonserious in another subject, or one subject may have experienced both a serious and nonserious event during the study.
|
|
Skin and subcutaneous tissue disorders
Hypertrichosis
|
2.0%
1/50
The same event may appear as both an AE and a SAE. However, what is presented are distinct events. An event may be categorized as serious in one subject and as nonserious in another subject, or one subject may have experienced both a serious and nonserious event during the study.
|
0.00%
0/16
The same event may appear as both an AE and a SAE. However, what is presented are distinct events. An event may be categorized as serious in one subject and as nonserious in another subject, or one subject may have experienced both a serious and nonserious event during the study.
|
|
Skin and subcutaneous tissue disorders
Increased tendency to bruise
|
2.0%
1/50
The same event may appear as both an AE and a SAE. However, what is presented are distinct events. An event may be categorized as serious in one subject and as nonserious in another subject, or one subject may have experienced both a serious and nonserious event during the study.
|
0.00%
0/16
The same event may appear as both an AE and a SAE. However, what is presented are distinct events. An event may be categorized as serious in one subject and as nonserious in another subject, or one subject may have experienced both a serious and nonserious event during the study.
|
|
Skin and subcutaneous tissue disorders
Nail disorder
|
10.0%
5/50
The same event may appear as both an AE and a SAE. However, what is presented are distinct events. An event may be categorized as serious in one subject and as nonserious in another subject, or one subject may have experienced both a serious and nonserious event during the study.
|
6.2%
1/16
The same event may appear as both an AE and a SAE. However, what is presented are distinct events. An event may be categorized as serious in one subject and as nonserious in another subject, or one subject may have experienced both a serious and nonserious event during the study.
|
|
Skin and subcutaneous tissue disorders
Night sweats
|
0.00%
0/50
The same event may appear as both an AE and a SAE. However, what is presented are distinct events. An event may be categorized as serious in one subject and as nonserious in another subject, or one subject may have experienced both a serious and nonserious event during the study.
|
6.2%
1/16
The same event may appear as both an AE and a SAE. However, what is presented are distinct events. An event may be categorized as serious in one subject and as nonserious in another subject, or one subject may have experienced both a serious and nonserious event during the study.
|
|
Skin and subcutaneous tissue disorders
Onychoclasis
|
4.0%
2/50
The same event may appear as both an AE and a SAE. However, what is presented are distinct events. An event may be categorized as serious in one subject and as nonserious in another subject, or one subject may have experienced both a serious and nonserious event during the study.
|
0.00%
0/16
The same event may appear as both an AE and a SAE. However, what is presented are distinct events. An event may be categorized as serious in one subject and as nonserious in another subject, or one subject may have experienced both a serious and nonserious event during the study.
|
|
Skin and subcutaneous tissue disorders
Pain of skin
|
2.0%
1/50
The same event may appear as both an AE and a SAE. However, what is presented are distinct events. An event may be categorized as serious in one subject and as nonserious in another subject, or one subject may have experienced both a serious and nonserious event during the study.
|
0.00%
0/16
The same event may appear as both an AE and a SAE. However, what is presented are distinct events. An event may be categorized as serious in one subject and as nonserious in another subject, or one subject may have experienced both a serious and nonserious event during the study.
|
|
Skin and subcutaneous tissue disorders
Pruritus
|
28.0%
14/50
The same event may appear as both an AE and a SAE. However, what is presented are distinct events. An event may be categorized as serious in one subject and as nonserious in another subject, or one subject may have experienced both a serious and nonserious event during the study.
|
6.2%
1/16
The same event may appear as both an AE and a SAE. However, what is presented are distinct events. An event may be categorized as serious in one subject and as nonserious in another subject, or one subject may have experienced both a serious and nonserious event during the study.
|
|
Skin and subcutaneous tissue disorders
Rash erythematous
|
4.0%
2/50
The same event may appear as both an AE and a SAE. However, what is presented are distinct events. An event may be categorized as serious in one subject and as nonserious in another subject, or one subject may have experienced both a serious and nonserious event during the study.
|
6.2%
1/16
The same event may appear as both an AE and a SAE. However, what is presented are distinct events. An event may be categorized as serious in one subject and as nonserious in another subject, or one subject may have experienced both a serious and nonserious event during the study.
|
|
Skin and subcutaneous tissue disorders
Rash maculo-papular
|
2.0%
1/50
The same event may appear as both an AE and a SAE. However, what is presented are distinct events. An event may be categorized as serious in one subject and as nonserious in another subject, or one subject may have experienced both a serious and nonserious event during the study.
|
6.2%
1/16
The same event may appear as both an AE and a SAE. However, what is presented are distinct events. An event may be categorized as serious in one subject and as nonserious in another subject, or one subject may have experienced both a serious and nonserious event during the study.
|
|
Skin and subcutaneous tissue disorders
Rash papular
|
2.0%
1/50
The same event may appear as both an AE and a SAE. However, what is presented are distinct events. An event may be categorized as serious in one subject and as nonserious in another subject, or one subject may have experienced both a serious and nonserious event during the study.
|
0.00%
0/16
The same event may appear as both an AE and a SAE. However, what is presented are distinct events. An event may be categorized as serious in one subject and as nonserious in another subject, or one subject may have experienced both a serious and nonserious event during the study.
|
|
Skin and subcutaneous tissue disorders
Rash pruritic
|
2.0%
1/50
The same event may appear as both an AE and a SAE. However, what is presented are distinct events. An event may be categorized as serious in one subject and as nonserious in another subject, or one subject may have experienced both a serious and nonserious event during the study.
|
0.00%
0/16
The same event may appear as both an AE and a SAE. However, what is presented are distinct events. An event may be categorized as serious in one subject and as nonserious in another subject, or one subject may have experienced both a serious and nonserious event during the study.
|
|
Skin and subcutaneous tissue disorders
Skin exfoliation
|
4.0%
2/50
The same event may appear as both an AE and a SAE. However, what is presented are distinct events. An event may be categorized as serious in one subject and as nonserious in another subject, or one subject may have experienced both a serious and nonserious event during the study.
|
6.2%
1/16
The same event may appear as both an AE and a SAE. However, what is presented are distinct events. An event may be categorized as serious in one subject and as nonserious in another subject, or one subject may have experienced both a serious and nonserious event during the study.
|
|
Skin and subcutaneous tissue disorders
Skin fissures
|
12.0%
6/50
The same event may appear as both an AE and a SAE. However, what is presented are distinct events. An event may be categorized as serious in one subject and as nonserious in another subject, or one subject may have experienced both a serious and nonserious event during the study.
|
0.00%
0/16
The same event may appear as both an AE and a SAE. However, what is presented are distinct events. An event may be categorized as serious in one subject and as nonserious in another subject, or one subject may have experienced both a serious and nonserious event during the study.
|
|
Skin and subcutaneous tissue disorders
Skin irritation
|
2.0%
1/50
The same event may appear as both an AE and a SAE. However, what is presented are distinct events. An event may be categorized as serious in one subject and as nonserious in another subject, or one subject may have experienced both a serious and nonserious event during the study.
|
0.00%
0/16
The same event may appear as both an AE and a SAE. However, what is presented are distinct events. An event may be categorized as serious in one subject and as nonserious in another subject, or one subject may have experienced both a serious and nonserious event during the study.
|
|
Skin and subcutaneous tissue disorders
Skin lesion
|
2.0%
1/50
The same event may appear as both an AE and a SAE. However, what is presented are distinct events. An event may be categorized as serious in one subject and as nonserious in another subject, or one subject may have experienced both a serious and nonserious event during the study.
|
0.00%
0/16
The same event may appear as both an AE and a SAE. However, what is presented are distinct events. An event may be categorized as serious in one subject and as nonserious in another subject, or one subject may have experienced both a serious and nonserious event during the study.
|
|
Vascular disorders
Flushing
|
2.0%
1/50
The same event may appear as both an AE and a SAE. However, what is presented are distinct events. An event may be categorized as serious in one subject and as nonserious in another subject, or one subject may have experienced both a serious and nonserious event during the study.
|
0.00%
0/16
The same event may appear as both an AE and a SAE. However, what is presented are distinct events. An event may be categorized as serious in one subject and as nonserious in another subject, or one subject may have experienced both a serious and nonserious event during the study.
|
|
Vascular disorders
Hypertension
|
2.0%
1/50
The same event may appear as both an AE and a SAE. However, what is presented are distinct events. An event may be categorized as serious in one subject and as nonserious in another subject, or one subject may have experienced both a serious and nonserious event during the study.
|
0.00%
0/16
The same event may appear as both an AE and a SAE. However, what is presented are distinct events. An event may be categorized as serious in one subject and as nonserious in another subject, or one subject may have experienced both a serious and nonserious event during the study.
|
|
Vascular disorders
Hypotension
|
2.0%
1/50
The same event may appear as both an AE and a SAE. However, what is presented are distinct events. An event may be categorized as serious in one subject and as nonserious in another subject, or one subject may have experienced both a serious and nonserious event during the study.
|
0.00%
0/16
The same event may appear as both an AE and a SAE. However, what is presented are distinct events. An event may be categorized as serious in one subject and as nonserious in another subject, or one subject may have experienced both a serious and nonserious event during the study.
|
Additional Information
Results disclosure agreements
- Principal investigator is a sponsor employee Pfizer has the right to review disclosures, requesting a delay of less than 60 days. Investigator will postpone single center publications until after disclosure of pooled data (all sites), less than 12 months from study completion/termination at all participating sites. Investigator may not disclose previously undisclosed confidential information other than study results.
- Publication restrictions are in place
Restriction type: OTHER