Evidence map›Paper›PMID 42748508›Full record

ArticleESMO open2026

Zolbetuximab plus chemotherapy versus immune checkpoint inhibitor regimens by programmed death-ligand 1 combined positive score in locally advanced or metastatic gastric or gastroesophageal junction adenocarcinoma: a Bayesian network meta-analysis.

K Shitara, S Y Rha, S J Klempner, F Lordick, R Ranganath, M Oh, R H Getzenberg, G Gourgioti, X Chai, H Yang

Abstract read
In one paragraph

Article in ESMO open, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

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2 · The registry

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

10 authors.

K ShitaraDepartment of Gastrointestinal Oncology, National Cancer Center Hospital East, Kashiwa, Chiba, Japan.
S Y RhaDepartment of Internal Medicine, Medical Oncology, Yonsei Cancer Center, Seoul, South Korea; Department of Internal Medicine, Yonsei University College of Medicine, Seoul, South Korea. Electronic address: rha7655@yuhs.ac.
S J KlempnerDepartment of Medicine, Massachusetts General Brigham Cancer Institute, Boston, USA.
F LordickDepartment of Medicine II, University of Leipzig Medical Center, Cancer Center Central Germany (CCCG), Leipzig, Germany.
R RanganathGlobal Medical Affairs, Astellas Pharma Global Development, Inc., Northbrook, USA.
M OhGlobal Medical Affairs, Astellas Pharma Global Development, Inc., Northbrook, USA.
R H GetzenbergGlobal Medical Affairs, Astellas Pharma Global Development, Inc., Northbrook, USA.
G GourgiotiEvidence Generation Advances Analytics, Astellas Pharma Ltd, Addlestone, UK.
X ChaiHEOR, Epidemiology & Market Access Practice, Analysis Group, Inc, Boston, USA.
H YangHEOR, Epidemiology & Market Access Practice, Analysis Group, Inc, Boston, USA.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundIn this network meta-analysis (NMA), efficacy of first-line (1L) zolbetuximab and immune checkpoint inhibitors (ICIs) was compared across programmed death-ligand 1 [PD-(L)1] combined positive score (CPS) levels in patients with locally advanced (LA) unresectable or metastatic gastric or gastroesophageal junction (mG/GEJ) adenocarcinoma in global trials. MATERIALS AND

methodsStudies evaluating zolbetuximab or ICIs plus chemotherapy as 1L treatments among adults with LA unresectable or mG/GEJ adenocarcinoma were included. A Bayesian fixed-effects NMA compared overall survival (OS) and progression-free survival (PFS) across treatments in PD-(L)1 CPS subgroups (CPS ≥1 to <5; ≥5 to <10; or ≥10). Because PD-(L)1 CPS is a biologically and clinically validated treatment effect modifier for ICIs, CPS-specific hazard ratios were used for ICIs but not zolbetuximab, which targets claudin 18 isoform 2 (CLDN18.2). Sensitivity analyses of PD-(L)1 CPS ≥10 leveraged patients with optimal zolbetuximab exposure-those who did not experience nausea/vomiting leading to inadequate dose exposure or discontinuation.

resultsFive regimens (zolbetuximab, pembrolizumab, tislelizumab, or nivolumab plus chemotherapy, and chemotherapy alone) were included. In PD-(L)1 CPS ≥1 to <5, zolbetuximab showed similar or numerically favorable OS and PFS versus ICIs. In PD-(L)1 CPS ≥5 to <10, zolbetuximab had numerically favorable OS and PFS versus ICIs. In PD-(L)1 CPS ≥10, ICIs had numerically favorable OS and PFS versus zolbetuximab. However, in sensitivity analyses, among patients with optimal zolbetuximab exposure, zolbetuximab showed similar OS and PFS to ICIs.

conclusionsThese findings support a biomarker-informed treatment approach in human epidermal growth factor receptor 2 (HER2)-negative, CLDN18.2-positive advanced gastric/GEJ adenocarcinoma. In PD-(L)1 CPS ≥1 to <10, zolbetuximab plus chemotherapy demonstrated consistent efficacy and may represent a relevant option beyond PD-(L)1-driven selection. In CPS ≥10, zolbetuximab remained clinically meaningful, with efficacy comparable to select ICI-based regimens when exposure is optimized. Results should be interpreted cautiously given these are indirect comparisons and warrant confirmation in prospective studies.

Indexed as

checkpoint inhibitorsCLDN18.2network meta-analysisstomach cancerzolbetuximab

Identifiers

PMID42748508
PMCPMC13595131

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.