Treatment-naive advanced non-small cell lung cancer without driver gene alteration NSCLC, advanced, driver oncogene negative
Conditions
Interventions
Group A
(1) Non-squamous NSCLC
CBDCA AUC 5 (day 1) + Pemetrexed 500 mg/m2 (day 1) + Pembrolizumab 200 mg/body (day 1), every 3 weeks, up to 4 cycles
Pemetrexed 500 mg/m2 (day 1) + Pembrolizumab 200 mg
D017428
Immune checkpoint inhibitor, Pembrolizumab, Nivolumab, Ipilimumab
Sponsors
OKAMOTO Isamu
Eligibility
Sex/Gender
All
Inclusion criteria
Inclusion criteria: (1) Cytologically (including biopsy) or histologically confirmed non-small cell lung cancer. (2) Clinical stage III without indication of definitive thoracic radiotherapy, stage IV, postoperative recurrent disease, or recurrence after radiation therapy. (3) No prior systemic chemotherapy. (4) No prior drug therapy that specifically target the T cell co-stimulation or checkpoint pathway, such as anti-PD-1 antibody, anti-PD-L1 antibody, and anti-CTLA-4 antibody. (5) No EGFR gene mutations for non-squamous cell carcinoma. (6) Negative or unknown ALK fusion gene, ROS1 fusion gene, BRAF (V600E) gene mutation, MET exon 14 skipping mutation, RET fusion gene, or NTRK fusion gene. (7) Over 20 years old. (8) Performance status 0 or 1. (9) Eligible regardless of PD-L1 (22C3) expression. (10) Measureable or non-measureable. (11) (i) No prior palliative radiation therapy for non-central nervous system metastases within 7 days (ii) No prior stereotactic irradiation and Gamma-knife for central nervous system metastases within 7 days (iii) No prior whole-brain irradiation within 14 days (iv) No prior pleural drainage within 7 days (v) No prior surgery with general anesthesia within 14 days (12) No symptomatic brain metastasis, leptomeningeal metastasis, or spinal cord metastasis requiring radiotherapy or surgical operation. (13) No active autoimmune disease. (14) No findings suggestive of interstitial lung disease or pulmonary fibrosis on the chest computed tomography. (15) Adequate organ funcion. (16) Written informed consent for this study. (17) Written informed consent for pretreatment stool collection for ancillary studies.
Exclusion criteria
Exclusion criteria: (1) Synchronous double or multiple cancer or metachronous double or multiple cancer within 2 years. (2) Infectious disease requiring systemic treatment. (3) Pyrexia of 38 degrees centigrade or higher. (4) During pregnancy, within 28 days of postparturition, or during lactation. (5) Psychological disorder difficult to participate in this clinical study. (6) Receiving continuous systemic corticosteroid or immunosuppressant treatment. (7) Diabetes mellitus uncontrollable with the appropriate treatment. (8) History of stroke within 1 year or frequent transient ischemic attacks. (9) Symptomatic congestive heart failure, unstable angina, or a history of myocardial infarction within 6 months. (10) Clinically serious arrhythmia on the electrocardiogram. (11) Positive for serum hepatitis B surface antigen. (12) HIV antibody positive. (13) Grade 2 or higher peripheral neuropathy. (14) Hypersensitivity to the ingredients / additives of carboplatin, pemetrexed, paclitaxel, nab-paclitaxel, pembrolizumab, nivolumab, and ipilimumab.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Overall Survival | — |
Secondary
| Measure | Time frame |
|---|---|
| Overall survival of patients with PD-L1 Tumor proportion score (TPS) <1%, Progression-free survival, Duration of response, Response proportion, Area under the survival curve from registration until 3 years later(restricted mean survival time: RMST), Adverse events, Serious adverse events, Quality of Life (Patient Reported Outcome) | — |
Contacts
Public ContactYoshimasa SHIRAISHI
Kyushu University Hospital
Outcome results
None listed