A Study of Apatinib Plus Docetaxel for Treatment of Advanced Non-squamous Non-small Cell Lung Cancer With Bone Metastases

NCT ID: NCT03127319

Last Updated: 2018-01-17

Basic Information

• Recruitment Status: UNKNOWN
• Clinical Phase: PHASE2
• Total Enrollment: 40 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2017-07-03
• Study Completion Date: 2019-12-31

Brief Summary

The purpose of this study is to assess the efficacy and safety of patients who receive apatinib plus docetaxel and zoledronic versus docetaxel and zoledronic alone as second line treatment for advanced non-squamous non-small cell lung cancer with bone metastases.

Conditions

Non-squamous Non-small Cell Lung Cancer

Study Design

• Allocation Method: RANDOMIZED
• Intervention Model: PARALLEL
• Primary Study Purpose: TREATMENT
• Blinding Strategy: NONE

Study Groups

apatinib and docetaxel zoledronic

apatinib 500mg qd po; docetaxel 60mg/m² iv q3w; zoledronic 4mg iv\>15min q4w until disease progression or intolerable toxicity or patients withdrawal of consent

Group Type: EXPERIMENTAL

apatinib docetaxel zoledronic

Intervention Type: DRUG

apatinib 500 mg qd p.o.docetaxel 60mg/m² iv q3w;zoledronic 4mg iv\>15min q4w until disease progression or intolerable toxicity or patients withdrawal of consent

docetaxel zoledronic

docetaxel 60mg/m² iv q3w;zoledronic 4mg iv\>15min q4w until disease progression or intolerable toxicity or patients withdrawal of consent

Group Type: ACTIVE_COMPARATOR

docetaxel zoledronic

Intervention Type: DRUG

docetaxel 60mg/m² iv q3w;zoledronic 4mg iv\>15min q4w until disease progression or intolerable toxicity or patients withdrawal of consent

Interventions

apatinib docetaxel zoledronic

apatinib 500 mg qd p.o.docetaxel 60mg/m² iv q3w;zoledronic 4mg iv\>15min q4w until disease progression or intolerable toxicity or patients withdrawal of consent

Intervention Type: DRUG

docetaxel zoledronic

docetaxel 60mg/m² iv q3w;zoledronic 4mg iv\>15min q4w until disease progression or intolerable toxicity or patients withdrawal of consent

Intervention Type: DRUG

Eligibility Criteria

Inclusion Criteria

1. Age:18 to 75 years old (man or female)

2. Pathologically diagnosed with metastatic or recurrent non-squamous non-small cell lung cancer

3. Patients with at least one evaluate lesions of the lung and bone metastases.(measuring≥10mm on spiral CT scan, satisfying the criteria in RECIST1.1 and WHO)

4. Refractory or failure of prior therapy

5. Life expectancy greater than or equal to 3 months

6. Eastern Cooperative Oncology Group (ECOG) performance status of 0-2

7. Major organ function has to meet the following criteria:

• For results of blood routine test (without blood transfusion within 14 days)

1. HB≥90g/L

2. ANC≥1.5×109/L

3. PLT≥180×109/L

• For results of blood biochemical test：

1. TBIL<1.5×ULN；

2. ALT and AST<2.5×ULN, but< 5×ULN if the transferase elevation is due to liver metastases；

3. Serum creatinine ≤1.25×ULN , or calculated creatinine clearance>45 ml/min(per the Cockcroft-Gault formula);

8. Women of childbearing age must have contraceptive measures or have test pregnancy (serum or urine) enroll the study before 7 days, and the results must be negative, and take the methods of contraception during the test and the last to have drugs after 8 weeks. Men must be contraception or has sterilization surgery during the test and the last to have drugs after 8 weeks;

9. Participants were willing to join in this study, and written informed consent, good adherence, cooperate with the follow-up.

Exclusion Criteria

1. Allergic to apatinib and docetaxel;

2. Have high blood pressure and antihypertensive drug treatment can not control (systolic blood pressure > 140 mmHg, diastolic blood pressure > 90 mmHg), with class Ⅱ and above coronary heart disease, arrhythmia (including QTc lengthened men > 450 ms, women > 470 ms) and class Ⅲ-Ⅳ cardiac insufficiency;

3. A variety of factors influencing oral drugs (such as unable to swallow, nausea, vomiting, chronic diarrhea and intestinal obstruction, etc.).

4. Patients with tendency of gastrointestinal bleeding, including the following: a local active ulcerative lesions, and defecate occult blood (+ +); Has melena and hematemesis in two months; For defecate occult blood (+) and primary lesions without surgical removal of the stomach tumor, requirement of gastroscopy, such as ulcer type of gastric cancer, and researchers think that may be gastrointestinal hemorrhage;

5. Coagulant function abnormality (INR > 1.5 ULN, APTT > 1.5 ULN), with bleeding tendency.

6. Patients with symptoms of central nervous system metastasis.

7. Pregnant or lactating women.

8. history of psychiatric drugs abuse and can't quit or patients with mental disorders.

9. Less than 4 weeks from the last clinical trial.

10. The researchers think inappropriate.

• Minimum Eligible Age: 18 Years
• Maximum Eligible Age: 75 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: No

Sponsors

Affiliated Hospital of Hebei University

OTHER

Sponsor Role: lead

Responsible Party

Aimin Zang

Director of oncology

Responsibility Role: PRINCIPAL_INVESTIGATOR

Locations

Affiliated Hospital of Hebei university

Baoding, Hebei, China

Site Status: RECRUITING

Countries

China

Central Contacts

Aimin Zang

Role: CONTACT

15175292891@163.com

13930881628

Facility Contacts

Aimin Zang

Role: primary

15175292891@163.com

13930881628

Other Identifiers

AHHU-2017AMZ01

Identifier Type: -

Identifier Source: org_study_id