drugset / Trial / NCT04702009

Efficacy and Safety of First-line Anti-PD-1/PD-L1 Monoclonal Antibody in Combination With Chemotherapy and Bronchoscopy-assisted Interventional Therapy in Patients With Advanced Central Non-small Cell Lung Cancer

NCT04702009

Phase 2/3 Completed 33 enrolled Shanghai Pulmonary Hospital, Shanghai, China
RandomizedParallel-groupQuadruple-blindTreatment

Summary

Lung cancer is one of the malignant tumors with high morbidity and mortality. Several PD-1/PD-L1 immune checkpoint inhibitors have been approved for the treatment of advanced non-small cell lung cancer (NSCLC). However, its overall effective population is only 20%, and even in studies of enriched populations (such as PD-L1 ≥ 50%), its single-drug effective rate is only about 40%. Therefore, this study aims to explore the efficacy and safety of anti-PD-1/PD-L1 monoclonal antibodies and chemotherapy in combination with bronchoscopy-assisted lnterventional therapy in the first-line treatment of advanced central non-small cell lung cancer. We conducted a randomized controlled, prospective clinical trial to examine the efficacy, safety, and mechanism of anti-PD-1/PD-L1 monoclonal antibodies, chemotherapy, in combination with bronchoscopy-assisted interventional therapy vs anti-PD-1/PD-L1 monoclonal antibody in combination with chemotherapy as the first-line treatment of patients with advanced central NSCLC.

Timeline

Start
2021-01-20
Primary completion
2025-10-17
Completion
2026-01-20

Drugs

EvaluationDrugModalityDoseRoute
Background Carboplatin Small molecule
Background Cisplatin Other / unclassified
Background Gemcitabine Small molecule
Background Pemetrexed Small molecule
Background Sintilimab Monoclonal antibody 200 mg Intravenous