Pembrolizumab plus Chemotherapy in Metastatic Non-Small-Cell Lung Cancer

Publikation: Bidrag til tidsskriftTidsskriftartikelForskningfagfællebedømt

  • Leena Gandhi
  • Delvys Rodríguez-Abreu
  • Shirish Gadgeel
  • Emilio Esteban
  • Enriqueta Felip
  • Flávia De Angelis
  • Manuel Domine
  • Philip Clingan
  • Maximilian J Hochmair
  • Steven F Powell
  • Susanna Y-S Cheng
  • Helge G Bischoff
  • Nir Peled
  • Francesco Grossi
  • Ross R Jennens
  • Martin Reck
  • Rina Hui
  • Edward B Garon
  • Michael Boyer
  • Belén Rubio-Viqueira
  • Silvia Novello
  • Takayasu Kurata
  • Jhanelle E Gray
  • John Vida
  • Ziwen Wei
  • Jing Yang
  • Harry Raftopoulos
  • M Catherine Pietanza
  • Marina C Garassino
  • KEYNOTE-189 Investigators
  • Michael Boyer
  • Victoria Bray
  • Baerin Ben Houghton
  • Sørensen, Jens Benn
  • Karin Holmskov Hansen
  • Miroslaw Jan Stelmach
  • William V. Walsh
  • John Wrangle
  • Stephen H. Wrzesinski

BACKGROUND: First-line therapy for advanced non-small-cell lung cancer (NSCLC) that lacks targetable mutations is platinum-based chemotherapy. Among patients with a tumor proportion score for programmed death ligand 1 (PD-L1) of 50% or greater, pembrolizumab has replaced cytotoxic chemotherapy as the first-line treatment of choice. The addition of pembrolizumab to chemotherapy resulted in significantly higher rates of response and longer progression-free survival than chemotherapy alone in a phase 2 trial.

METHODS: In this double-blind, phase 3 trial, we randomly assigned (in a 2:1 ratio) 616 patients with metastatic nonsquamous NSCLC without sensitizing EGFR or ALK mutations who had received no previous treatment for metastatic disease to receive pemetrexed and a platinum-based drug plus either 200 mg of pembrolizumab or placebo every 3 weeks for 4 cycles, followed by pembrolizumab or placebo for up to a total of 35 cycles plus pemetrexed maintenance therapy. Crossover to pembrolizumab monotherapy was permitted among the patients in the placebo-combination group who had verified disease progression. The primary end points were overall survival and progression-free survival, as assessed by blinded, independent central radiologic review.

RESULTS: After a median follow-up of 10.5 months, the estimated rate of overall survival at 12 months was 69.2% (95% confidence interval [CI], 64.1 to 73.8) in the pembrolizumab-combination group versus 49.4% (95% CI, 42.1 to 56.2) in the placebo-combination group (hazard ratio for death, 0.49; 95% CI, 0.38 to 0.64; P<0.001). Improvement in overall survival was seen across all PD-L1 categories that were evaluated. Median progression-free survival was 8.8 months (95% CI, 7.6 to 9.2) in the pembrolizumab-combination group and 4.9 months (95% CI, 4.7 to 5.5) in the placebo-combination group (hazard ratio for disease progression or death, 0.52; 95% CI, 0.43 to 0.64; P<0.001). Adverse events of grade 3 or higher occurred in 67.2% of the patients in the pembrolizumab-combination group and in 65.8% of those in the placebo-combination group.

CONCLUSIONS: In patients with previously untreated metastatic nonsquamous NSCLC without EGFR or ALK mutations, the addition of pembrolizumab to standard chemotherapy of pemetrexed and a platinum-based drug resulted in significantly longer overall survival and progression-free survival than chemotherapy alone. (Funded by Merck; KEYNOTE-189 ClinicalTrials.gov number, NCT02578680 .).

OriginalsprogEngelsk
TidsskriftThe New England Journal of Medicine
Vol/bind378
Udgave nummer22
Sider (fra-til)2078-2092
ISSN0028-4793
DOI
StatusUdgivet - 2018

ID: 218609945