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Nivolumab Plus Chemotherapy versus Placebo Plus Chemotherapy in Korean Patients with HER2-Negative, Untreated, Unresectable Advanced or Recurrent Gastric or Gastroesophageal Junction Cancer: Subgroup Analysis of a Randomized, Multicenter, Double-Blind Phase 3 Trial (ATTRACTION-4)

  • Yoon Koo Kang*
  • , Min Hee Ryu
  • , Do Youn Oh
  • , Sang Cheul Oh
  • , Sun Young Rha
  • , Keun Wook Lee
  • , Ik Joo Chung
  • , Sung Yong Oh
  • , Sun Jin Sym
  • , Won Ki Kang
  • , Jong Gwang Kim
  • , Byoung Yong Shim
  • , In Ho Kim
  • , Jin Young Kim
  • , Eun Kee Song
  • , Hyo Jin Lee
  • , Seok Yun Kang
  • , Dong Hoe Koo
  • , So Yeon Oh
  • *Corresponding author for this work
  • University of Ulsan
  • Seoul National University
  • Korea University
  • Yonsei University
  • Chonnam National University
  • Dong-A University
  • Gachon University
  • Samsung Medical Center, Sungkyunkwan university
  • Kyungpook National University
  • The Catholic University of Korea
  • Keimyung University
  • Chungnam National University
  • Ajou University
  • Kangbuk Samsung Hospital
  • Pusan National University

Research output: Contribution to journal › Journal article › peer-review

Abstract

Purpose We report the safety and efficacy of nivolumab+chemotherapy for first-line treatment of advanced or recurrent gastric or gastroesophageal junction cancer in the Korean subpopulation of the ATTRACTION-4 clinical trial. Materials and Methods ATTRACTION-4 (NCT02746796) was a double-blind, randomized, placebo-controlled clinical trial of patients aged ≥ 20 years with histologically confirmed unresectable advanced or recurrent gastric or gastroesophageal junction cancer. Patients received nivolumab or placebo, both combined with physician-choice chemotherapy (oxaliplatin plus oral S-1 [tegafur–gimeracil–oteracil] [SOX] or oral capecitabine [CAPOX]). Results Overall, 464 patients were initially screened in Korea and 291 were randomized to nivolumab+chemotherapy (total/SOX/ CAPOX: 148/66/82 patients) or placebo+chemotherapy (total/SOX/CAPOX: 143/61/82 patients). Centrally assessed progressionfree survival (median, 14.75 vs. 8.34 months; hazard ratio [HR], 0.53; 95% confidence interval [CI], 0.39 to 0.73; p < 0.001), overall survival (19.7 vs. 14.9 months; HR, 0.78; 95% CI, 0.60 to 1.02; p=0.065), overall response rate (54.7% vs. 47.6%), and duration of response (16.03 vs. 9.86 months) favored nivolumab+chemotherapy vs. placebo+chemotherapy. Grade ≥ 3 treatment-related adverse events (TRAEs) (56.1% vs. 44.1%), and any-grade endocrine (9.5% vs. 4.2%), hepatic (23.0% vs. 14.7%), hypersensitivity and infusion reactions (15.5% vs. 7.0%), renal (4.1% vs. 0.7%), and skin (44.6% vs. 23.1%) TRAEs tended to be more frequent in the nivolumab+chemotherapy group. Conclusion These findings demonstrate the clinical benefit of nivolumab combined with chemotherapy (either SOX or CAPOX) for first-line treatment of gastric cancer/gastroesophageal junction cancer in Korean patients.

Original languageEnglish
Pages (from-to)846-859
Number of pages14
JournalCancer Research and Treatment
Volume58
Issue number3
DOIs
StatePublished - 2026.07

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

Keywords

  • Capecitabine
  • Gastroesophageal junction cancer
  • Nivolumab
  • Oxaliplatin-based chemotherapy
  • S-1
  • Stomach neoplasms

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