Evidence map›Paper›PMID 42318470›Full record

ArticleFrontiers in oncology2026

Continuing immune checkpoint inhibitors beyond progression versus switching to non-ICI therapy in advanced gastric cancer: a real-world study.

Guangxi Wang, Xiaonan Lu, Yunmei Wang, Xiang Wang, Ruoxuan Wang, Jinyu Jia

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Article in Frontiers in oncology, 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

What it found

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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

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

6 authors.

Guangxi Wang *Department of Medical Oncology, Shaanxi Provincial Cancer Hospital, Xi'an, China.
Xiaonan Lu *Department of Ultrasound, The First Affiliated Hospital of Air Force Medical University, Xi'an, China.
Yunmei WangDepartment of Medical Oncology, Shaanxi Provincial Cancer Hospital, Xi'an, China.
Xiang WangDepartment of Medical Oncology, Shaanxi Provincial Cancer Hospital, Xi'an, China.
Ruoxuan WangDepartment of Medical Oncology, Shaanxi Provincial Cancer Hospital, Xi'an, China.
Jinyu JiaDepartment of Medical Oncology, Shaanxi Provincial Cancer Hospital, Xi'an, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: The optimal second-line therapy for advanced gastric/gastroesophageal junction cancer (GC/GEJC) following progression on first-line immuno-chemotherapy remains undefined. This study aimed to compare the efficacy and safety of continuing an immune checkpoint inhibitor beyond progression (CIBP) versus switching to a non-ICI regimen (non-CIBP). Methods: In this single-center, retrospective study, we enrolled 169 patients with GC/GEJC who progressed after first-line ICI plus chemotherapy. Based on the second-line therapeutic decision, patients were categorized into either the CIBP group (n=120; to continue ICI with or without combined therapy) or the non-CIBP group (n=49; to switch to a non-ICI regimen). The primary endpoints were progression-free survival (PFS) and overall survival (OS). Results: The CIBP group demonstrated significantly improved median PFS (4.4 vs. 3.0 months; hazard ratio [HR]=0.47, 95% CI: 0.33-0.67; p<0.001) and median OS (9.5 vs. 6.4 months; HR = 0.51, 95% CI: 0.34-0.77; p=0.0012) compared to the non-CIBP group. The survival benefit of CIBP remained robust after multivariable adjustment (PFS HR = 0.54, p=0.003; OS HR = 0.65, p=0.044) and propensity score matching. Subgroup analyses revealed that patients with PD-L1 expression ≥1%, those who achieved an objective response to first-line therapy, or those with a first-line PFS ≥6 months derived the greatest benefit from CIBP. The safety profile was manageable and comparable between the two groups. Conclusion: In this real-world cohort, continuing ICI beyond progression was associated with significantly superior survival outcomes compared to switching to non-ICI regimens, with a manageable safety profile. CIBP represents a valid and promising second-line strategy for selected patients with advanced GC/GEJC following first-line immuno-chemotherapy failure.

Indexed as

advanced gastric cancerefficacyimmune checkpoint inhibitorreal-world studysafetytreatment beyond progression

Identifiers

PMID42318470
PMCPMC13272025

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