drugset / Trial / NCT02220894

Study of Pembrolizumab (MK-3475) Versus Platinum-Based Chemotherapy for Participants With Programmed Cell Death-Ligand 1 (PD-L1)-Positive Advanced or Metastatic Non-Small Cell Lung Cancer (MK-3475-042/KEYNOTE-042)

NCT02220894 ↗

Phase 3 Completed 1274 enrolled Merck Sharp & Dohme LLC
RandomizedParallel-groupOpen-labelTreatment

Summary

In this study, participants with programmed cell death ligand 1 (PD-L1)-positive non-small cell lung cancer (NSCLC) will be randomized to receive single agent pembrolizumab for up to 35 treatments or standard of care (SOC) platinum-based chemotherapy (carboplatin + paclitaxel or carboplatin + pemetrexed for 4 to 6 21-day cycles). Participants in the platinum-based chemotherapy arms with non-squamous tumor histologies may receive pemetrexed maintenance therapy after the 4 to 6 cycles of chemotherapy. The primary study hypothesis is that pembrolizumab prolongs overall survival (OS) compared to SOC chemotherapy.

Timeline

Start
2014-10-30
Primary completion
2018-09-04
Completion
2022-09-12

Outcome

Met primary endpoint

registry analysis (superiority test); Pembrolizumab vs Chemotherapy (SOC Treatment); p = 0.0003; Hazard Ratio (HR) 0.70 (95% CI 0.58 to 0.86) NCT02220894 ↗

registry analysis (superiority test); Pembrolizumab vs Chemotherapy (SOC Treatment); p = 0.0012; Hazard Ratio (HR) 0.77 (95% CI 0.65 to 0.91) NCT02220894 ↗

registry analysis (superiority test); Pembrolizumab vs Chemotherapy (SOC Treatment); p = 0.0013; Hazard Ratio (HR) 0.82 (95% CI 0.71 to 0.93) NCT02220894 ↗

Publications

Drugs

EvaluationDrugModalityDoseRoute
Comparator Carboplatin Small molecule 5 unknown Intravenous
Comparator Carboplatin Small molecule 6 unknown Intravenous
Comparator Paclitaxel Small molecule 200 mg/m2 Intravenous
Subject Pembrolizumab Monoclonal antibody 200 mg Intravenous
Comparator Pemetrexed Small molecule 500 mg/m2 Intravenous