Evidence map›Paper›PMID 42812796›Full record

ArticleBiologics : targets & therapy2026

Apatinib Plus PD-1 Blockade versus Chemotherapy After Prior Immunotherapy in Advanced Gastric or Gastroesophageal Junction Adenocarcinoma: A Retrospective Cohort Study.

Rui-Xin Li, Hong-Wei Yang, Yun-Fei Zhang, Xin-Yu Liu

Abstract read
In one paragraph

Article in Biologics : targets & therapy, 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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0citing papers in PubMed
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1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

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

The trial behind it

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3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

4 authors.

Rui-Xin LiDepartment of gastrointestinal surgery, the First Affiliated Hospital of Zhengzhou University, Zhengzhou, Henan, 450052, People's Republic of China.
Hong-Wei YangDepartment of gastrointestinal surgery, the First Affiliated Hospital of Zhengzhou University, Zhengzhou, Henan, 450052, People's Republic of China.
Yun-Fei ZhangDepartment of gastrointestinal surgery, the First Affiliated Hospital of Zhengzhou University, Zhengzhou, Henan, 450052, People's Republic of China.
Xin-Yu LiuDepartment of gastrointestinal surgery, the First Affiliated Hospital of Zhengzhou University, Zhengzhou, Henan, 450052, People's Republic of China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Objective: To compare clinical outcomes and safety of apatinib plus programmed death-1 (PD-1) blockade versus single-agent chemotherapy in patients with advanced gastric or gastroesophageal junction (G/GEJ) adenocarcinoma previously exposed to immune checkpoint inhibitors (ICIs). Methods: This single-center retrospective cohort included 117 adults with HER2-negative advanced G/GEJ adenocarcinoma treated after discontinuation of an ICI-containing regimen. 59 patients received apatinib plus PD-1 blockade (AP group) and 58 received single-agent chemotherapy (CT group). The primary endpoint was overall survival (OS), secondary endpoints included progression-free survival (PFS), objective response rate (ORR), disease control rate (DCR), duration of response (DoR), and treatment-related adverse events (TRAEs). Survival was analyzed using Kaplan-Meier methods and Cox regression, stabilized inverse probability of treatment weighting (IPTW) and prespecified sensitivity analyses were used to assess robustness to measured confounding. Results: ORR was numerically higher in the AP group than in the CT group (20.3% vs 8.6%, Conclusion: Apatinib plus PD-1 blockade was associated with longer survival and greater disease control than single-agent chemotherapy. Given the single-center retrospective design, limited sample size, treatment heterogeneity, incomplete biomarker characterization, and potential residual confounding, these findings are hypothesis-generating, do not establish causality, and require prospective validation.

Indexed as

apatinibchemotherapyeffectivenessgastric cancergastroesophageal junction adenocarcinomaimmune checkpoint inhibitor rechallengePD-1 blockadessafety

Identifiers

PMID42812796
PMCPMC13621946

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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.