Updated Analysis From KEYNOTE-189: Pembrolizumab or Placebo Plus Pemetrexed and Platinum for Previously Untreated Metastatic Nonsquamous Non–Small-Cell Lung Cancer

Shirish M. Gadgeel(The Barbara Ann Karmanos Cancer Institute), Delvys Rodríguez‐Abreu(Universidad de Las Palmas de Gran Canaria), Giovanna Speranza(Hôpital Charles-Le Moyne), Emilio Esteban(Hospital Universitario Central de Asturias), Enriqueta Felip(Vall d'Hebron Institute of Oncology), Manuel Dómine(Hospital Universitario Fundación Jiménez Díaz), Rina Hui(The University of Sydney), Maximilian J. Hochmair, Philip R. Clingan(Wollongong Hospital), Steven Powell(Sanford Health), Susanna Y. Cheng(Sunnybrook Health Science Centre), Helge Bischoff, Nir Peled(Soroka Medical Center), Francesco Grossi(Fondazione IRCCS Ca' Granda Ospedale Maggiore Policlinico), Ross Jennens(Epworth Hospital), Martin Reck(German Center for Lung Research), Edward B. Garon(University of California, Los Angeles), Silvia Novello(Ospedale San Luigi Gonzaga), Belén Rubio‐Viqueira(Hospital Universitario Quirónsalud Madrid), Michael Boyer(Chris O’Brien Lifehouse), Takayasu Kurata(Kansai Medical University), Jhanelle E. Gray(Moffitt Cancer Center), Jing Yang(Merck & Co., Inc., Rahway, NJ, USA (United States)), Tuba Öcek Baş(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)
Journal of Clinical Oncology
March 9, 2020
Cited by 1,147Open Access
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Abstract

PURPOSE: In KEYNOTE-189, first-line pembrolizumab plus pemetrexed-platinum significantly improved overall survival (OS) and progression-free survival (PFS) compared with placebo plus pemetrexed-platinum in patients with metastatic nonsquamous non‒small-cell lung cancer (NSCLC), irrespective of tumor programmed death-ligand 1 (PD-L1) expression. We report an updated analysis from KEYNOTE-189 (ClinicalTrials.gov: NCT02578680). METHODS: Patients were randomly assigned (2:1) to receive pemetrexed and platinum plus pembrolizumab (n = 410) or placebo (n = 206) every 3 weeks for 4 cycles, then pemetrexed maintenance plus pembrolizumab or placebo for up to a total of 35 cycles. Eligible patients with disease progression in the placebo-combination group could cross over to pembrolizumab monotherapy. Response was assessed per RECIST (version 1.1) by central review. No alpha was assigned to this updated analysis. RESULTS: As of September 21, 2018 (median follow-up, 23.1 months), the updated median (95% CI) OS was 22.0 (19.5 to 25.2) months in the pembrolizumab-combination group versus 10.7 (8.7 to 13.6) months in the placebo-combination group (hazard ratio [HR], 0.56; 95% CI, 0.45 to 0.70]). Median (95% CI) PFS was 9.0 (8.1 to 9.9) months and 4.9 (4.7 to 5.5) months, respectively (HR, 0.48; 95% CI, 0.40 to 0.58). Median (95% CI) time from randomization to objective tumor progression on next-line treatment or death from any cause, whichever occurred first (progression-free-survival-2; PFS-2) was 17.0 (15.1 to 19.4) months and 9.0 (7.6 to 10.4) months, respectively (HR, 0.49; 95% CI, 0.40 to 0.59). OS and PFS benefits with pembrolizumab were observed regardless of PD-L1 expression or presence of liver/brain metastases. Incidence of grade 3-5 adverse events was similar in the pembrolizumab-combination (71.9%) and placebo-combination (66.8%) groups. CONCLUSION: First-line pembrolizumab plus pemetrexed-platinum continued to demonstrate substantially improved OS and PFS in metastatic nonsquamous NSCLC, regardless of PD-L1 expression or liver/brain metastases, with manageable safety and tolerability.


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