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First-Line Nivolumab Plus Chemotherapy for Advanced Gastric, Gastroesophageal Junction, and Esophageal Adenocarcinoma: 3-Year Follow-Up of the Phase III CheckMate 649 Trial

  • Yelena Y. Janjigian
  • , Jaffer A. Ajani
  • , Markus Moehler
  • , Lin Shen
  • , Marcelo Garrido
  • , Carlos Gallardo
  • , Lucjan Wyrwicz
  • , Kensei Yamaguchi
  • , James M. Cleary
  • , Elena Elimova
  • , Michalis Karamouzis
  • , Ricardo Bruges
  • , Tomasz Skoczylas
  • , Arinilda Bragagnoli
  • , Tianshi Liu
  • , Mustapha Tehfe
  • , Thomas Zander
  • , Ruben Kowalyszyn
  • , Roberto Pazo-Cid
  • , Michael Schenker
  • Kynan Feeny, Rui Wang, Ming Lei, Clara Chen, Raheel Nathani, Kohei Shitara
  • Memorial Sloan-Kettering Cancer Center
  • MD Anderson Cancer Center
  • Johannes Gutenberg University Mainz
  • Peking University
  • Pontificia Universidad Católica de Chile
  • Fundación Arturo López Pérez
  • Klinika Onkologii i Radioterapii
  • Japanese Foundation for Cancer Research
  • Dana-Farber Cancer Institute
  • Princess Margaret Hospital
  • Laiko Hospital
  • Instituto Nacional de Cancerología - Colombia
  • Medical University of Lublin
  • Hospital de Câncer de Barretos
  • Zhongshan Hospital
  • Montreal Diabetes Research Center and University of Montreal Hospital Research Centre (CRCHUM)
  • University of Cologne
  • Clinica Viedma S.A.
  • Hospital Miguel Servet
  • Sfantul Nectarie Oncology Center
  • St John of God Health Care
  • Bristol-Myers Squibb
  • National Cancer Center Japan

Research output: Contribution to journalArticlepeer-review

188 Scopus citations

Abstract

Clinical trials frequently include multiple end points that mature at different times. The initial report, typically based on the primary end point, may be published when key planned co-primary or secondary analyses are not yet available. Clinical Trial Updates provide an opportunity to disseminate additional results from studies, published in JCO or elsewhere, for which the primary end point has already been reported.We report 3-year efficacy and safety results from the phase III CheckMate 649 trial. Patients with previously untreated advanced or metastatic gastroesophageal adenocarcinoma were randomly assigned to nivolumab plus chemotherapy or chemotherapy. Primary end points were overall survival (OS) and progression-free survival (PFS) by blinded independent central review (BICR) in patients whose tumors expressed PD-L1 combined positive score (CPS) ≥5. With 36.2-month minimum follow-up, for patients with PD-L1 CPS ≥5, the OS hazard ratio (HR) for nivolumab plus chemotherapy versus chemotherapy was 0.70 (95% CI, 0.61 to 0.81); 21% versus 10% of patients were alive at 36 months, respectively; the PFS HR was 0.70 (95% CI, 0.60 to 0.81); 36-month PFS rates were 13% versus 8%, respectively. The objective response rate (ORR) per BICR was 60% (95% CI, 55 to 65) with nivolumab plus chemotherapy versus 45% (95% CI, 40 to 50) with chemotherapy; median duration of response was 9.6 months (95% CI, 8.2 to 12.4) versus 7.0 months (95% CI, 5.6 to 7.9), respectively. Nivolumab plus chemotherapy also continued to show improvement in OS, PFS, and ORR versus chemotherapy in the overall population. Adding nivolumab to chemotherapy maintained clinically meaningful long-term survival benefit versus chemotherapy alone, with an acceptable safety profile, supporting the continued use of nivolumab plus chemotherapy as standard first-line treatment for advanced gastroesophageal adenocarcinoma.

Original languageEnglish
Pages (from-to)2012-2020
Number of pages9
JournalJournal of Clinical Oncology
Volume42
Issue number17
DOIs
StatePublished - 10 Jun 2024
Externally publishedYes

UN SDGs

This output contributes to the following UN Sustainable Development Goals (SDGs)

  1. SDG 3 - Good Health and Well-being
    SDG 3 Good Health and Well-being

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