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Domvanalimab and zimberelimab in advanced gastric, gastroesophageal junction or esophageal cancer: a phase 2 trial

Authors
 Janjigian, Yelena Y.  ;  Oh, Do-Youn  ;  Pelster, Meredith  ;  Wainberg, Zev A.  ;  Prusty, Subhransu  ;  Nelson, Sandahl  ;  DuPage, Amy  ;  Thompson, Amy  ;  Koralek, Daniel O.  ;  Sison, Edward Allan R.  ;  Rha, Sun Young 
Citation
 NATURE MEDICINE, Vol.31(12) : 4274-4280, 2025-12 
Journal Title
NATURE MEDICINE
ISSN
 1078-8956 
Issue Date
2025-12
MeSH
Adenocarcinoma* / drug therapy ; Adenocarcinoma* / pathology ; Adult ; Aged ; Aged, 80 and over ; Antibodies, Monoclonal, Humanized* / administration & dosage ; Antibodies, Monoclonal, Humanized* / adverse effects ; Antibodies, Monoclonal, Humanized* / therapeutic use ; Antineoplastic Combined Chemotherapy Protocols / administration & dosage ; Antineoplastic Combined Chemotherapy Protocols / adverse effects ; Antineoplastic Combined Chemotherapy Protocols / therapeutic use ; Esophageal Neoplasms* / drug therapy ; Esophageal Neoplasms* / pathology ; Esophagogastric Junction* / drug effects ; Esophagogastric Junction* / pathology ; Female ; Fluorouracil / administration & dosage ; Fluorouracil / therapeutic use ; Humans ; Leucovorin / administration & dosage ; Leucovorin / therapeutic use ; Male ; Middle Aged ; Organoplatinum Compounds / administration & dosage ; Programmed Cell Death 1 Receptor / antagonists & inhibitors ; Progression-Free Survival ; Receptors, Immunologic / antagonists & inhibitors ; Stomach Neoplasms* / drug therapy ; Stomach Neoplasms* / pathology
Abstract
Dual inhibition of T cell immunoreceptor with immunoglobulin and ITIM domain (TIGIT) and programmed cell death protein 1 (PD-1) may enhance antitumor immunity in advanced gastroesophageal cancers. Here we report the EDGE-Gastric study, an ongoing, multicenter, international, phase 2 study with three cohorts, one in the first-line setting (cohort A) and two in the second-line or greater setting (cohorts B and C). Cohort A comprises four arms: two nonrandomized (A1 and A2) and two randomized (A3 and A4). In arm A1, presented here, dual blockade of TIGIT and PD-1 with domvanalimab (Fc-silent anti-TIGIT) and zimberelimab (anti-PD-1) plus oxaliplatin, leucovorin, fluorouracil (FOLFOX) was evaluated in patients with previously untreated advanced HER2-negative gastric, gastroesophageal junction or esophageal adenocarcinoma. Among 41 treated patients, the confirmed objective response rate was 59% (90% confidence interval (CI) 44.5-71.6%), median progression-free survival was 12.9 months (90% CI 9.8-14.6 months) and median overall survival was 26.7 months (90% CI 18.4 months to not estimable (NE)). In patients with tumor area positivity >= 1% (PD-L1 positive) and tumor area positivity >= 5% (PD-L1 high), respectively, the objective response rate was 62% (90% CI 45.1-77.1%) and 69% (90% CI 45.2-86.8%), median progression-free survival was 13.2 months (90% CI 11.3-15.2 months) and 14.5 months (90% CI 11.3 months-NE), and median overall survival was 26.7 months (90% CI 19.5 months-NE) and not reached (90% CI 17.4 months-NE). Immune-related adverse events were reported in 27% of patients; the safety profile was consistent with that reported for anti-PD-1 plus platinum-based chemotherapy. Dual TIGIT and PD-1 blockade with domvanalimab and zimberelimab plus chemotherapy demonstrated encouraging efficacy, and the regimen is being evaluated in the phase 3 STAR-221 trial. ClinicalTrials.gov identifier: NCT05329766.
Files in This Item:
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DOI
10.1038/s41591-025-04022-w
Appears in Collections:
1. College of Medicine (의과대학) > Dept. of Internal Medicine (내과학교실) > 1. Journal Papers
Yonsei Authors
Rha, Sun Young(라선영) ORCID logo https://orcid.org/0000-0002-2512-4531
URI
https://ir.ymlib.yonsei.ac.kr/handle/22282913/209948
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