Evidence map›Paper›PMID 40597880›Full record

ArticleBMC cancer2025

Efficacy and safety of anti-PD-1 antibodies plus small molecule anti-angiogenic drugs and chemotherapy in gastric cancer peritoneal metastasis: a multicenter real-world study.

Fen Guo, Deqiang Wang, Luyao Zhang, Yueyu Fang, Jianming Shi, Guoqiang Wang, Mingyang Yu, Yuxin Feng, Liyu Wang, Ying Feng and 1 more

Abstract readClinical StudyMulticenter Study
In one paragraph

Article in BMC cancer, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact
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

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

1 citing paper in PubMed.

  1. Article
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

11 authors.

Fen Guo *Department of Oncology, the Affiliated Suzhou Hospital of Nanjing Medical University, Suzhou Municipal Hospital, No.16 Baita West Road, Suzhou, Jiangsu Province, 215000, China.
Deqiang Wang *Department of Oncology, Digestive Disease Institute &, Cancer Institute of Jiangsu University, Affiliated Hospital of Jiangsu University, No.438 Jiefang Road, Zhenjiang, Jiangsu Province, 212000, China.
Luyao Zhang *Department of Oncology, the Affiliated Suzhou Hospital of Nanjing Medical University, Suzhou Municipal Hospital, No.16 Baita West Road, Suzhou, Jiangsu Province, 215000, China.
Yueyu FangDepartment of Oncology, The Affiliated Nanjing Pukou People's Hospital of Jiangsu Health Vocational College, Nanjing Pukou People's Hospital, Liangjiang Hospital Southeast University, No.166 Shanghe Street, Nanjing, 211800, Jiangsu Province, China.
Jianming ShiDepartment of Oncology, the Affiliated Suzhou Hospital of Nanjing Medical University, Suzhou Municipal Hospital, No.16 Baita West Road, Suzhou, Jiangsu Province, 215000, China.
Guoqiang WangDepartment of Oncology, the Affiliated Suzhou Hospital of Nanjing Medical University, Suzhou Municipal Hospital, No.16 Baita West Road, Suzhou, Jiangsu Province, 215000, China.
Mingyang YuDepartment of Oncology, the Affiliated Suzhou Hospital of Nanjing Medical University, Suzhou Municipal Hospital, No.16 Baita West Road, Suzhou, Jiangsu Province, 215000, China.
Yuxin FengDepartment of Oncology, the Affiliated Suzhou Hospital of Nanjing Medical University, Suzhou Municipal Hospital, No.16 Baita West Road, Suzhou, Jiangsu Province, 215000, China.
Liyu WangDepartment of Oncology, the Affiliated Suzhou Hospital of Nanjing Medical University, Suzhou Municipal Hospital, No.16 Baita West Road, Suzhou, Jiangsu Province, 215000, China. liyuw2316@126.com.
Ying FengDepartment of Oncology, the Affiliated Suzhou Hospital of Nanjing Medical University, Suzhou Municipal Hospital, No.16 Baita West Road, Suzhou, Jiangsu Province, 215000, China. fengying91521@yeah.net.
XiaoFeng ChenDepartment of Oncology, The First Affiliated Hospital of Nanjing Medical University, No.300 Guangzhou Road, Nanjing, Jiangsu Province, 210029, China. chenxiaofengnjmu@163.com.

Funding

Nanjing Medical University Gusu School Youth Talent Development Program GSKY20250533Qilu Foundation Project of Nanjing Medical University KY218CXY2024020Suzhou Integrated Chinese and Western Medicine Research Fund SKYD2023253Suzhou "Science and Education for Health" Youth Science and Technology Programme KJXW2023032
6 · The paper itself

Abstract

backgroundImmunotherapy combined with chemotherapy has emerged as the first-line standard treatment for advanced gastric cancer. However, obvious survival benefits in patients with peritoneal metastatic gastric cancer remain elusive. The combination of anti-angiogenic agents and immunotherapy has shown synergistic effects. However, currently there are no relevant reports on the efficacy and safety of immunotherapy combined with anti-angiogenic agents and chemotherapy in patients with gastric cancer peritoneal metastatic.

methodsWe conducted a multicenter, retrospective clinical study in four independent healthcare facilities, enrolling advanced gastric cancer patients with peritoneal metastatic who received immunotherapy in combination with anti-angiogenic agents and chemotherapy between January 2020 and March 2023. All patients were treated with triple combination regimen for at least two and up to eight cycles before being adjusted for immunotherapy and targeted therapy. This study observed overall survival (OS) and time to treatment failure (TTF), as well as an exploratory analysis of the impact of ascites and peritoneal metastases on the prognosis of all patients.

resultsThis study enrolled 30 eligible patients in the final analysis cohort. The median TTF and OS were 7.03 months [95% confidence interval (CI), 4.17-9.89] and 13.33 months (95% CI: 10.96-15.71), respectively. The 6-month and 12-month OS rates were 83.0% and 53.0%, respectively. The objective response rate (ORR) was 58.3%, and the disease control rate (DCR) was 83.3% in 12 patients who were evaluated for response with at least one measurable lesion. Exploratory subgroup analysis revealed that the median TTF and OS in the subgroup without ascites were significantly better than those in the subgroup with ascites, with a median TTF of 9.03 vs. 4.63 months (χ

conclusionsThe combination of immunotherapy, anti-angiogenic agents, and chemotherapy demonstrated therapeutic potential with a manageable safety profile in patients with peritoneal metastatic gastric cancer. These findings should be interpreted cautiously due to the inherent limitations of retrospective analyses and need to be validated through prospective randomized controlled trials to establish clinical efficacy and optimize patient selection criteria.

Indexed as

Angiogenesis InhibitorsAntineoplastic Combined Chemotherapy ProtocolsImmune Checkpoint InhibitorsPeritoneal NeoplasmsStomach NeoplasmsAdultAgedFemaleHumansMaleMiddle AgedPrognosisProgrammed Cell Death 1 ReceptorRetrospective StudiesTreatment OutcomeAngiogenesis InhibitorsImmune Checkpoint InhibitorsProgrammed Cell Death 1 ReceptorAnti-angiogenic agentsChemotherapyGastric cancer peritoneal metastasisImmunotherapyRetrospective study

Identifiers

PMID40597880
PMCPMC12211162

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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.