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

Leena Gandhi(NYU Langone’s Laura and Isaac Perlmutter Cancer Center), Delvys Rodríguez‐Abreu(Hospital Universitario Insular de Gran Canaria), Shirish M. Gadgeel(The Barbara Ann Karmanos Cancer Institute), Emilio Esteban(Hospital Universitario Central de Asturias), Enriqueta Felip(Vall d'Hebron Institute of Oncology), Flávia De Angelis, Manuel Dómine(Hospital Universitario Fundación Jiménez Díaz), Philip R. Clingan, Maximilian J. Hochmair(Otto Wagner Hospital), Steven Powell(Sanford Health), Susanna Y. Cheng(Sunnybrook Health Science Centre), Helge Bischoff, Nir Peled(Rabin Medical Center), Francesco Grossi(Ospedale Policlinico San Martino), Ross Jennens(Epworth Hospital), Martin Reck(German Center for Lung Research), Rina Hui(The University of Sydney), Edward B. Garon(University of California, Los Angeles), Michael Boyer(Chris O’Brien Lifehouse), Belén Rubio‐Viqueira(Hospital Universitario Quirónsalud Madrid), Silvia Novello(Ospedale San Luigi Gonzaga), Takayasu Kurata(Kansai Medical University), Jhanelle E. Gray(Moffitt Cancer Center), John Vida(Merck & Co., Inc., Rahway, NJ, USA (United States)), Ziwen Wei(Merck & Co., Inc., Rahway, NJ, USA (United States)), Jing Yang(Merck & Co., Inc., Rahway, NJ, USA (United States)), Harry Raftopoulos(Merck & Co., Inc., Rahway, NJ, USA (United States)), M. Catherine Pietanza(Merck & Co., Inc., Rahway, NJ, USA (United States)), Marina Chiara Garassino(Fondazione IRCCS Istituto Nazionale dei Tumori)
New England Journal of Medicine
April 16, 2018
Cited by 6,570Open Access
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Abstract

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 .).


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