Evidence map›Paper›PMID 41313676›Full record

ArticleJournal of evidence-based medicine2025

Prevalence of DNA Mismatch Repair Deficiencies in Multiple Solid Tumor Types in China.

Xiaohua Shi, Xianghong Yang, Jingping Yun, Xiangshan Fan, Yingyong Hou, Zhe Wang, Peng Li, Jieyu Chen, Dongxian Jiang, Longyun Chen and 5 more

Abstract read
In one paragraph

Article in Journal of evidence-based medicine, 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

15 authors.

Xiaohua ShiDepartment of Pathology, Peking Union Medical College Hospital, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing, China.ORCID https://orcid.org/0000-0002-5007-5540
Xianghong YangDepartment of Pathology, Shengjing Hospital of China Medical University, Shenyang, Liaoning, China.
Jingping YunDepartment of Pathology, Sun Yat-sen University Cancer Center, Guangzhou, Guangdong, China.
Xiangshan FanDepartment of Pathology, The Affiliated Drum Tower Hospital of Nanjing University Medical School, Nanjing, Jiangsu, China.
Yingyong HouDepartment of Pathology, Zhongshan Hospital, Fudan University, Shanghai, China.
Zhe WangDepartment of Pathology, Shengjing Hospital of China Medical University, Shenyang, Liaoning, China.
Peng LiDepartment of Pathology, Sun Yat-sen University Cancer Center, Guangzhou, Guangdong, China.
Jieyu ChenDepartment of Pathology, The Affiliated Drum Tower Hospital of Nanjing University Medical School, Nanjing, Jiangsu, China.
Dongxian JiangDepartment of Pathology, Zhongshan Hospital, Fudan University, Shanghai, China.
Longyun ChenDepartment of Pathology, Peking Union Medical College Hospital, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing, China.
Yan WangValue & Implementation, Global Medical & Scientific Affairs, MSD China, Shanghai, China.
Rubentiran RamarPrecision Medicine, MSD International GmbH, Singapore, Singapore.
Michael Thomas WongPrecision Medicine, MSD International GmbH, Singapore, Singapore.
Song Ling PoonPrecision Medicine, MSD International GmbH, Singapore, Singapore.
Zhiyong LiangDepartment of Pathology, Peking Union Medical College Hospital, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing, China.

Funding

MSD China
6 · The paper itself

Abstract

aimMicrosatellite instability (MSI) as a result of deficient deoxyribonucleic acid (DNA) mismatch repair (dMMR) is a key contributor to the development of tumors with a high mutation rate and cancer-specific neoantigens. dMMR identification can be beneficial for selection of immune checkpoint inhibitor (ICI) therapy-eligible patients. While multiple studies have focused on dMMR prevalence in colorectal cancer (CRC), fewer investigate the prevalence of dMMR in tumor types besides CRC, especially in Chinese patients. In this study, we aimed to determine the prevalence of dMMR in China across five gastrointestinal and gynecological tumor types.

methodsTissue samples from Chinese patients with advanced endometrial, ovarian, cervical, biliary tract, or gastric metastatic or unresectable solid tumors were tested for dMMR status using immunohistochemistry with the Ventana MMR RxDx panel. Data were analyzed to determine the prevalence of dMMR for each tumor type.

resultsA total of 748 patients were included in the study, representing five tumor types. Prevalence of dMMR varied across tumor types, with an overall prevalence of 9.4%. Patients with endometrial tumors had the highest proportion of patients with dMMR at 49/164 (29.9%). Patients with cervical tumors had the lowest prevalence of dMMR with 6/221 (2.7%) patients. The prevalence of dMMR was similar across most demographic characteristics. In the dMMR population, co-occurring MLH1 and PMS2 protein loss across all tumor types was observed most commonly, in 48/70 (68.6%) patients.

conclusionsThese data highlight the importance of dMMR testing in patients with advanced solid tumors in China to optimize biomarker testing and treatment decisions.

Indexed as

DNA Mismatch RepairMicrosatellite InstabilityNeoplasmsAdultAgedChinaFemaleHumansMaleMiddle AgedPrevalenceChinaDNA mismatch repair deficiencyepidemiologyimmune checkpoint inhibitormicrosatellite instabilityprevalence

Identifiers

PMID41313676
PMCPMC12750482

What Socratic 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 Socratic graph.