Evidence map›Paper›PMID 40540446›Full record

SynthesisInternational journal of surgery (London, England)2025

Efficacy and safety of immunotherapy-based neoadjuvant regimens in locally advanced gastric cancer: a meta-analysis based on high-quality clinical trials.

Chen Liang, Zhiyuan Yu, Rui Li, Tao Xu, Siyu Hou, Junfu Zheng, Weina Chen, Chunzeng Jia, Yan Gao, Pengji Gao and 1 more

Abstract readMeta-AnalysisSystematic Review
In one paragraph

Synthesis in International journal of surgery (London, England), 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed, 1 pooled it
–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

6 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
  2. Article
  3. Article
  4. Article
  5. Article
  6. 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.

Chen LiangDepartment of Gastroenterology, Beijing Jishuitan Hospital, Capital Medical University, Beijing, China.
Zhiyuan YuDepartment of General Surgery, Beijing Friendship Hospital, Capital Medical University, Beijing, China.
Rui LiSchool of Medicine, Nankai University, Tianjin, China.
Tao XuDepartment of Gastroenterology, Beijing Jishuitan Hospital, Capital Medical University, Beijing, China.
Siyu HouDepartment of Gastroenterology, Beijing Jishuitan Hospital, Capital Medical University, Beijing, China.
Junfu ZhengDepartment of Gastroenterology, Beijing Jishuitan Hospital, Capital Medical University, Beijing, China.
Weina ChenDepartment of Gastroenterology, Beijing Jishuitan Hospital, Capital Medical University, Beijing, China.
Chunzeng JiaDepartment of Gastroenterology, Beijing Jishuitan Hospital, Capital Medical University, Beijing, China.
Yan GaoDepartment of Gastroenterology, Beijing Jishuitan Hospital, Capital Medical University, Beijing, China.
Pengji GaoDepartment of General Surgery, Beijing Jishuitan Hospital, Capital Medical University, Beijing, China.
Lei LiDepartment of Gastroenterology, Beijing Jishuitan Hospital, Capital Medical University, Beijing, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundThe integration of chemotherapy, targeted therapy, and immunotherapy has emerged as the latest research focus for locally advanced gastric cancer (LAGC). This study aims to evaluate the efficacy and safety of various immunotherapy-based neoadjuvant regimens for LAGC.

methodsPubMed, EmBase, and Cochrane Library databases were systematically searched based on the predefined inclusion criteria. Subsequently, the Stata software (version 17) was employed to separately integrate the outcome indicators of the single- and dual-arm studies, thereby systematically assessing the antitumor effects of three distinct immunotherapy-based regimens: neoadjuvant immunotherapy plus chemotherapy (NICT), neoadjuvant chemotherapy plus targeted therapy (NCTT), and NICT plus targeted therapy (NICTT).

results16 high-quality Phase II prospective single-arm clinical studies and 7 dual-arm clinical studies were selected. The pooled results from the single-arm studies indicated that immune-based neoadjuvant therapy could increase the rates of pathological complete response (pCR), severe treatment-related adverse events (TRAEs), 1- and 3-year disease-free survival (DFS), as well as 1- and 3-year overall survival (OS) to 20%, 30%, 91%, 74%, 94%, and 81%, respectively. Pairwise meta-analysis indicated that both the NICT and NICTT groups achieved higher rates of pCR, major pathological response (MPR), and complete resection (R0 resection) compared to the neoadjuvant chemotherapy (NCT) group, with the NICTT group exhibiting more pronounced effects. The NICTT group exhibited a significantly higher risk of experiencing severe TRAEs compared to the NCT group. ICIs + XELOX appeared to be a more appropriate NICT regimen, as it effectively enhanced the tumor response rate while inducing less severe TRAEs. Tumors exhibiting positive expression of PD-L1 or microsatellite instable (MSI) demonstrated a higher level of responsiveness to the NICT regimen.

conclusionsImmunotherapy-based neoadjuvant regimens exhibit an enhanced potential for promoting tumor regression; however, caution is warranted due to the elevated risk of severe TRAEs.

Indexed as

ImmunotherapyNeoadjuvant TherapyStomach NeoplasmsHumansTreatment OutcomeimmunotherapyLAGCmeta-analysisneoadjuvant regimenstargeted therapy

Identifiers

PMID40540446
PMCPMC12527757

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

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.