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Domvanalimab and zimberelimab in advanced gastric, gastroesophageal junction or esophageal cancer: a phase 2 trial
| DC Field | Value | Language |
|---|---|---|
| dc.contributor.author | Janjigian, Yelena Y. | - |
| dc.contributor.author | Oh, Do-Youn | - |
| dc.contributor.author | Pelster, Meredith | - |
| dc.contributor.author | Wainberg, Zev A. | - |
| dc.contributor.author | Prusty, Subhransu | - |
| dc.contributor.author | Nelson, Sandahl | - |
| dc.contributor.author | DuPage, Amy | - |
| dc.contributor.author | Thompson, Amy | - |
| dc.contributor.author | Koralek, Daniel O. | - |
| dc.contributor.author | Sison, Edward Allan R. | - |
| dc.contributor.author | Rha, Sun Young | - |
| dc.date.accessioned | 2026-01-19T07:59:06Z | - |
| dc.date.available | 2026-01-19T07:59:06Z | - |
| dc.date.created | 2026-01-02 | - |
| dc.date.issued | 2025-12 | - |
| dc.identifier.issn | 1078-8956 | - |
| dc.identifier.uri | https://ir.ymlib.yonsei.ac.kr/handle/22282913/209948 | - |
| dc.description.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. | - |
| dc.language | English | - |
| dc.publisher | Nature Publishing Company | - |
| dc.relation.isPartOf | NATURE MEDICINE | - |
| dc.relation.isPartOf | NATURE MEDICINE | - |
| dc.subject.MESH | Adenocarcinoma* / drug therapy | - |
| dc.subject.MESH | Adenocarcinoma* / pathology | - |
| dc.subject.MESH | Adult | - |
| dc.subject.MESH | Aged | - |
| dc.subject.MESH | Aged, 80 and over | - |
| dc.subject.MESH | Antibodies, Monoclonal, Humanized* / administration & dosage | - |
| dc.subject.MESH | Antibodies, Monoclonal, Humanized* / adverse effects | - |
| dc.subject.MESH | Antibodies, Monoclonal, Humanized* / therapeutic use | - |
| dc.subject.MESH | Antineoplastic Combined Chemotherapy Protocols / administration & dosage | - |
| dc.subject.MESH | Antineoplastic Combined Chemotherapy Protocols / adverse effects | - |
| dc.subject.MESH | Antineoplastic Combined Chemotherapy Protocols / therapeutic use | - |
| dc.subject.MESH | Esophageal Neoplasms* / drug therapy | - |
| dc.subject.MESH | Esophageal Neoplasms* / pathology | - |
| dc.subject.MESH | Esophagogastric Junction* / drug effects | - |
| dc.subject.MESH | Esophagogastric Junction* / pathology | - |
| dc.subject.MESH | Female | - |
| dc.subject.MESH | Fluorouracil / administration & dosage | - |
| dc.subject.MESH | Fluorouracil / therapeutic use | - |
| dc.subject.MESH | Humans | - |
| dc.subject.MESH | Leucovorin / administration & dosage | - |
| dc.subject.MESH | Leucovorin / therapeutic use | - |
| dc.subject.MESH | Male | - |
| dc.subject.MESH | Middle Aged | - |
| dc.subject.MESH | Organoplatinum Compounds / administration & dosage | - |
| dc.subject.MESH | Programmed Cell Death 1 Receptor / antagonists & inhibitors | - |
| dc.subject.MESH | Progression-Free Survival | - |
| dc.subject.MESH | Receptors, Immunologic / antagonists & inhibitors | - |
| dc.subject.MESH | Stomach Neoplasms* / drug therapy | - |
| dc.subject.MESH | Stomach Neoplasms* / pathology | - |
| dc.title | Domvanalimab and zimberelimab in advanced gastric, gastroesophageal junction or esophageal cancer: a phase 2 trial | - |
| dc.type | Article | - |
| dc.contributor.googleauthor | Janjigian, Yelena Y. | - |
| dc.contributor.googleauthor | Oh, Do-Youn | - |
| dc.contributor.googleauthor | Pelster, Meredith | - |
| dc.contributor.googleauthor | Wainberg, Zev A. | - |
| dc.contributor.googleauthor | Prusty, Subhransu | - |
| dc.contributor.googleauthor | Nelson, Sandahl | - |
| dc.contributor.googleauthor | DuPage, Amy | - |
| dc.contributor.googleauthor | Thompson, Amy | - |
| dc.contributor.googleauthor | Koralek, Daniel O. | - |
| dc.contributor.googleauthor | Sison, Edward Allan R. | - |
| dc.contributor.googleauthor | Rha, Sun Young | - |
| dc.identifier.doi | 10.1038/s41591-025-04022-w | - |
| dc.relation.journalcode | J02296 | - |
| dc.identifier.eissn | 1546-170X | - |
| dc.identifier.pmid | 41109921 | - |
| dc.contributor.affiliatedAuthor | Rha, Sun Young | - |
| dc.identifier.scopusid | 2-s2.0-105019074448 | - |
| dc.identifier.wosid | 001595844200001 | - |
| dc.citation.volume | 31 | - |
| dc.citation.number | 12 | - |
| dc.citation.startPage | 4274 | - |
| dc.citation.endPage | 4280 | - |
| dc.identifier.bibliographicCitation | NATURE MEDICINE, Vol.31(12) : 4274-4280, 2025-12 | - |
| dc.identifier.rimsid | 90561 | - |
| dc.type.rims | ART | - |
| dc.description.journalClass | 1 | - |
| dc.description.journalClass | 1 | - |
| dc.subject.keywordPlus | PEMBROLIZUMAB PLUS CHEMOTHERAPY | - |
| dc.subject.keywordPlus | TIGIT | - |
| dc.subject.keywordPlus | EFFICACY | - |
| dc.type.docType | Article; Early Access | - |
| dc.description.isOpenAccess | Y | - |
| dc.description.journalRegisteredClass | scie | - |
| dc.description.journalRegisteredClass | scopus | - |
| dc.relation.journalWebOfScienceCategory | Biochemistry & Molecular Biology | - |
| dc.relation.journalWebOfScienceCategory | Cell Biology | - |
| dc.relation.journalWebOfScienceCategory | Medicine, Research & Experimental | - |
| dc.relation.journalResearchArea | Biochemistry & Molecular Biology | - |
| dc.relation.journalResearchArea | Cell Biology | - |
| dc.relation.journalResearchArea | Research & Experimental Medicine | - |
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