Evidence map›Paper›PMID 42411163›Full record

ArticleJournal of gastric cancer2026

Optimizing Postoperative Management in Deficient Mismatch Repair/Microsatellite Instability-High Gastric or Gastroesophageal Junction Adenocarcinoma: A Multicenter Retrospective Study.

Hua Liu, Hongmei Xu, Yakun Wang, Zimin Liu, Jia Wei, Zhiwei Chang, Yi Li, Jialin Lu, Boya Wang, Zhiruo Zhou and 4 more

Abstract readMulticenter Study
In one paragraph

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

0numbers the graph read from it
0cells of the map it votes in
0citing 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

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

14 authors.

Hua Liu *Department of Gastroenterology, China-Japan Friendship Hospital, Beijing, China.
Hongmei Xu *Department of Medical Oncology, First Hospital of Qinhuangdao, Qinhuangdao, China.ORCID https://orcid.org/0000-0001-5787-4516
Yakun Wang *State Key Laboratory of Holistic Integrative Management of Gastrointestinal Cancers, Beijing Key Laboratory of Carcinogenesis and Translational Research, Department of Gastrointestinal Oncology, Peking University Cancer Hospital & Institute, Beijing, China.ORCID https://orcid.org/0000-0001-5579-2998
Zimin LiuDepartment of Oncology, The Affiliated Hospital of Qingdao University, Qingdao, China.ORCID https://orcid.org/0000-0003-3104-4287
Jia WeiDepartment of Oncology, Nanjing Drum Tower Hospital, Affiliated Hospital of Medical School, Nanjing University, Nanjing, China.ORCID https://orcid.org/0000-0003-3024-8878
Zhiwei ChangDepartment of Oncology, The First Affiliated Hospital of Zhengzhou University, Zhengzhou, China.
Yi LiDepartment of Oncology, The First Affiliated Hospital of Zhengzhou University, Zhengzhou, China.
Jialin LuKey Laboratory of Carcinogenesis and Translational Research (Ministry of Education/Beijing), Department of Gastrointestinal Oncology, Peking University Cancer Hospital & Institute, Beijing, China.ORCID https://orcid.org/0009-0000-4541-9065
Boya WangKey Laboratory of Carcinogenesis and Translational Research (Ministry of Education/Beijing), Department of Gastrointestinal Oncology, Peking University Cancer Hospital & Institute, Beijing, China.ORCID https://orcid.org/0000-0003-4771-1785
Zhiruo ZhouKey Laboratory of Carcinogenesis and Translational Research (Ministry of Education/Beijing), Department of Gastrointestinal Oncology, Peking University Cancer Hospital & Institute, Beijing, China.ORCID https://orcid.org/0009-0002-6713-3855
Wenfei LiKey Laboratory of Carcinogenesis and Translational Research (Ministry of Education/Beijing), Department of Gastrointestinal Oncology, Peking University Cancer Hospital & Institute, Beijing, China.ORCID https://orcid.org/0009-0000-3582-8025
Lin CongKey Laboratory of Carcinogenesis and Translational Research (Ministry of Education/Beijing), Department of Gastrointestinal Oncology, Peking University Cancer Hospital & Institute, Beijing, China.ORCID https://orcid.org/0000-0001-6160-0454
Yu SunKey Laboratory of Carcinogenesis and Translational Research (Ministry of Education), Department of Pathology, Peking University Cancer Hospital & Institute, Beijing, China. sunyu_bch@163.com.ORCID https://orcid.org/0000-0003-3024-0331
Xiaotian ZhangState Key Laboratory of Holistic Integrative Management of Gastrointestinal Cancers, Beijing Key Laboratory of Carcinogenesis and Translational Research, Department of Gastrointestinal Oncology, Peking University Cancer Hospital & Institute, Beijing, China.ORCID https://orcid.org/0000-0001-6936-2622

Funding

Beijing Hospitals Authority Ascent Plan DFL20241104Capital's Funds for Health Improvement and Research 2024-1-1021National Science and Technology Major Project for Noncommunicable Chronic Diseases 2024ZD0520600Natural Science Foundation of Beijing Municipality L234003Peking University Cancer Hospital Clinical Research Youth Fund QNJJ2022025Science Foundation of Peking University Cancer Hospital QNJJ202202
6 · The paper itself

Abstract

purposeThe benefit of chemotherapy in locally advanced gastroesophageal cancer with deficient mismatch repair (dMMR) or microsatellite instability-high (MSI-H) remains uncertain. This study aimed to identify optimal postoperative management strategies for dMMR/MSI-H gastric or gastroesophageal junction (EGJ) adenocarcinoma. MATERIALS AND

methodsPatients with pathologically confirmed stage II-IVA dMMR/MSI-H gastric or EGJ adenocarcinoma who underwent D2 gastrectomy between 2015 and 2022 were retrospectively enrolled from 4 centers. Postoperative management strategies included observation, chemotherapy, immune checkpoint inhibitors (ICIs), or ICIs combined with chemotherapy (ICI-chemo). The primary endpoint was 2-year event-free survival (EFS), and the secondary endpoints were EFS and overall survival (OS).

resultsA total of 156 patients were included in the analysis. The highest 2-year EFS was observed in the ICI-chemo group (87.5%), followed by the observation group (86.7%) and the ICI monotherapy group (86.5%), whereas chemotherapy alone yielded the lowest rate (75.7%). Patients with earlier-stage disease had significantly lower risks of progression (hazard ratio [HR], 0.29; 95% confidence interval [CI], 0.16-0.53) and death (HR, 0.30; 95% CI, 0.14-0.64). EFS improved progressively from chemotherapy to observation and further to ICI-containing regimens across stages. In stage III-IVA disease, ICI monotherapy significantly improved OS compared with chemotherapy (HR, 0.28; P=0.038), with a favorable trend observed for ICI-chemo (HR, 0.32).

conclusionsPathological stage is an independent prognostic factor in resectable dMMR/MSI-H gastric and EGJ adenocarcinoma. Adjuvant chemotherapy alone demonstrated limited benefit, whereas ICI-based regimens were associated with improved outcomes, supporting their use in high-risk patients.

Indexed as

AdenocarcinomaDNA Mismatch RepairEsophageal NeoplasmsEsophagogastric JunctionMicrosatellite InstabilityPostoperative CareStomach NeoplasmsAgedFemaleGastrectomyHumansMaleMiddle AgedRetrospective StudiesAdjuvants, pharmaceuticDNA mismatch repairEsophagogastric junctionGastric cancerMicrosatellite instability

Identifiers

PMID42411163
PMCPMC13342272

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Registered trials

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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.