Efficacy and Safety of CRT, Durvalumab and Surgery for SST
NCT ID: NCT04465968
Last Updated: 2020-07-10
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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NOT_YET_RECRUITING
PHASE3
84 participants
INTERVENTIONAL
2020-09-01
2030-08-31
Brief Summary
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Detailed Description
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Conditions
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Study Design
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NA
SINGLE_GROUP
TREATMENT
NONE
Study Groups
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CRT + Durvalumab ± Surgery + Durvalumab
Concurrent chemoradiotherapy (cisplatin+S-1+radiotherapy 66Gy)+2 courses of durvalumab followed by Surgery and adjuvant durvalumab for resectable SST or chemoradiotherapy (cisplatin+S-1+radiotherapy 66Gy) followed by maintenance durvalumab for unresectable SST.
Cisplatin
Cisplatin 60 mg/m2, IV, day 1
S1
80 - 120 mg/day, PO, day 1-14
concurrent radiotherapy
66 Gy/33 Fr
Durvalumab
preoperative durvalumab therapy within 28 days after chemoradiotherapy. Two courses are given every two weeks.
Surgery
Surgery will be performed between day 15 and day 42 of the second course of preoperative durvalumab therapy after confirming that all surgical operation criteria are met.
Durvalumab
(For resectable SST) Postoperative durvalumab therapy will be started between day 28 and day 63 with the day of surgery as Day 1. Twenty-two courses are given as a 2-week course.
Drug: Durvalumab 10 mg/kg/body, IV, day 1 (For unreectable SST) Additional durvalumab therapy between day 15 and day 28 of the second course of preoperative durvalumab therapy.
Twenty-two courses are given as 2-week course. Drug: Durvalumab 10 mg/kg/body, IV, day 1
Interventions
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Cisplatin
Cisplatin 60 mg/m2, IV, day 1
S1
80 - 120 mg/day, PO, day 1-14
concurrent radiotherapy
66 Gy/33 Fr
Durvalumab
preoperative durvalumab therapy within 28 days after chemoradiotherapy. Two courses are given every two weeks.
Surgery
Surgery will be performed between day 15 and day 42 of the second course of preoperative durvalumab therapy after confirming that all surgical operation criteria are met.
Durvalumab
(For resectable SST) Postoperative durvalumab therapy will be started between day 28 and day 63 with the day of surgery as Day 1. Twenty-two courses are given as a 2-week course.
Drug: Durvalumab 10 mg/kg/body, IV, day 1 (For unreectable SST) Additional durvalumab therapy between day 15 and day 28 of the second course of preoperative durvalumab therapy.
Twenty-two courses are given as 2-week course. Drug: Durvalumab 10 mg/kg/body, IV, day 1
Eligibility Criteria
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Inclusion Criteria
2. Meet all of the following (UICC-TNM classification 8th edition). I. Regarding the primary lesion, meet one of the following on chest CT. i. Direct invasion of the chest wall at or above the height of the first rib (at least invasion of the parietal pleura) ii. Direct invasion of the subclavian artery or vein II. Regarding regional lymph nodes, meet either of the following by chest CT and FDG-PET/CT. Metastasis is also considered if lymph node metastasis is determined by either chest CT or FDG-PET/CT.
i. cN0 ii. cN1 and no metastases to #10, #11, and #12 lymph nodes iii. cN3 (ipsilateral supraclavicular lymph node metastasis) and no metastases in regional lymph nodes (N1 and N2) other than "#13, #14 lymph nodes" III. No distant metastases (including intrapulmonary metastases in the same ling lobe and in a different lung lobe on the same side) on imaging tests including FDG-PET/CT
3. It is judged that radical resection is possible by lobectomy (including bilobectomy for 2 lobes), which satisfies the following \[1\] and \[2\].
I. The board respiratory surgeon judges that none of the following is true based on the image findings.
i. There is vertebral body infiltration that requires total spondylectomy ii. Presence of spinal cord infiltration iii. Invaded trachea or tracheal bifurcation iv. Invasion of aortic arch or ascending aorta v. Invading brachial plexus at C8 or higher vi. Esophageal infiltration that requires esophageal reconstruction for resection vii. Pneumonectomy is required for radical resection II. Meet all of the following. i. Predicted postoperative forced expiratory volume of 1 second (FEV1.0) ≥ 800 mL within 56 days before registration ii. SpO2 \> 93% (room air) with the latest inspection value within 14 days before registration
4. Consult with the radiotherapy doctor and it is judged that all of the following are met.
I. Radiation therapy is possible according to the protocol II. The irradiation field does not reach the hilum
5. The age of the registration date is 20 years or older and 75 years or yonger.
6. Performance status (PS) is 0 or 1 according to ECOG standards (PS must be described in medical records)
7. The presence or absence of measurable lesions is not required.
8. No history of following surgery irrespective of whether for a benign or malignant lesion.
I. Thoracoscopic surgery or thoracotomy with excision of the affected lung or esophagus or mediastinum (however, a history of thoracoscopic surgery without wedge resection or lung, esophagus, or mediastinal resection (eg, pleural biopsy)) is allowed) II. Median sternotomy surgery (with or without organ resection) III. Pulmonary resection other than wedge resection of the contralateral lung (whether open-heart surgery or thoracoscopic surgery)
9. There is no history of chemotherapy, including treatment for other cancer types (including molecular targeted therapies and immune checkpoint inhibitors). However, the history of drug therapy as adjuvant therapy is allowed if it was completed more than 3 years ago. In addition, a history of hormone therapy for other cancer types is allowed.
10. If there is a history of radiotherapy including other cancer types, the lung, hilum, mediastinum, and supraclavicular fossa are not included in the irradiation field.
11. Chest CT does not show interstitial pneumonia or pulmonary fibrosis.
12. No history of complication of autoimmune disease or chronic or recurrent autoimmune disease. However, patients with type 1 diabetes which is well controlled by appropriate treatment, hyperthyroidism/hypothyroidism that requires only antithyroid drug/hormone replacement therapy, autoimmune skin disease that does not require systemic treatment (Pemphigus, psoriasis vulgaris, pemphigus vulgaris, vitiligo), and celiac disease controlled only by dietary control are regarded as eligible if they have been inactive in the past 5 years, even with a history of autoimmune complications or history.
13. No surgical treatment with general anesthesia within 14 days (2 weeks) before registration.
14. No systemic administration of steroids, other immunosuppressive drugs, or immunoglobulins within 28 days (4 weeks) before registration. However, those that meet the following conditions are allowed.
I. Intranasal/inhalation/topical steroid injection or local steroid injection (for example, intra-articular injection) II. Systemic administration of steroid drugs at a dose of 10 mg/day or less in terms of prednisolone III. Steroids as premedication (eg CT premedication)
15. Can be taken orally.
16. No ischemic changes were observed on the latest 12-lead ECG within 28 days before registration. However, if a 12-lead electrocardiogram shows ischemic changes, echocardiography, exercise electrocardiography, etc. should be performed, and if it is judged that new treatment for ischemic heart disease is not necessary, it is qualified.
17. The latest inspection value within 14 days before registration (possible on the same day two weeks before the registration date) satisfies all of the following.
I. White blood cell count ≧4,000/mm3 II. Hemoglobin ≥ 11.0 g/dL (no blood transfusion within 14 days before the blood sampling date of the test used for registration) III. Platelet count ≧10×104 /mm3 IV. Total bilirubin ≤ 2.0 mg/dL V. AST ≤ 75 U/L VI. ALT ≤ 75 U/L VII. Serum creatinine ≤ 1.2 mg/dL
18. Written informed consent from the patient to participate in the study.
19. The attending physician can judge that the enrolled patients understand the treatment and evaluation schedule of this study and can comply with them.
Exclusion Criteria
2. Has an infectious disease that requires systemic treatment (including active pulmonary tuberculosis).
3. When registering, a fever of 38.0°C or higher is generated.
4. Women who are pregnant, possibly pregnant, within 28 days of delivery, or breastfeeding. A man who wants a partner to become pregnant. Or a reproductive male or female patient who is not willing to use an effective contraceptive by Week 13 (Day 91) after the last dose of durvalumab (see 6.4.7.).
5. Participation in the study is considered to be difficult due to the combination of mental illnesses or symptoms that impair daily life.
6. Continuous systemic administration (oral or intravenous) of steroid drugs or other immunosuppressive drugs in excess of 10 mg/day in terms of prednisolone.
7. With uncontrolled diabetes.
8. With uncontrolled hypertension.
9. A gastrointestinal disorder accompanied by uncontrolled diarrhea.
10. With unstable angina (angina with onset or exacerbation of attack within the last 3 weeks) or a history of myocardial infarction within 6 months.
11. Poor valvular heart disease, dilated cardiomyopathy, hypertrophic cardiomyopathy, congestive heart failure, and arrhythmia.
12. Chest CT reveals severe emphysema.
13. Either HBs antigen, HCV antibody, or HIV1/2 antibody is positive.
14. Continuous use of flucytosine (Ancotil®) is required.
15. Participating in another clinical trial (excluding observational studies) during the 6 months prior to enrollment.
16. A history of allogeneic organ transplant.
17. A history of active primary immunodeficiency.
18. Live vaccines (BCG, polio, measles-rubella mixture, measles, rubella, mumps, chickenpox, yellow fever, rotavirus, etc.) have been administered within 30 days before registration.
19. Has hypersensitivity or allergy to the test drug or its additives used in this test.
20 Years
75 Years
ALL
No
Sponsors
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AstraZeneca
INDUSTRY
Japan Agency for Medical Research and Development
OTHER_GOV
Japan Clinical Oncology Group
OTHER
National Cancer Center Hospital East
OTHER
Responsible Party
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Masahiro Tsuboi
MD
Central Contacts
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Other Identifiers
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JCOG1807C
Identifier Type: -
Identifier Source: org_study_id
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