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International journal of cancer

July 31, 2026 · via Europe PMC

Deficient Mismatch Repair Represents a Distinct Molecular Feature of Early-Onset Colorectal Cancer in Chinese Single-Center Cohort.

Tang D, Mao Z, Lan S, +8 more, Wang Y.

Journal ArticleAbstract only — full text under license

AI summary — for doctors, generated from the abstract only

In a large Chinese single-center cohort, early-onset colorectal cancer had more advanced features and roughly double the odds of deficient mismatch repair compared with later-onset disease.

What was studied

A retrospective review of 4,159 colorectal cancers with complete MMR immunohistochemistry at West China Hospital (2008-2023), comparing early-onset (<50 years) with late-onset cases.

Key findings

  • EOCRC had more poor differentiation, T4 tumors, nodal involvement and advanced stage
  • Early onset independently associated with dMMR (adjusted OR 2.27, 95% CI 1.60-3.22)
  • Association persisted without documented family history (adjusted OR 1.95)
  • MMR protein loss patterns differed by family history

Clinical relevance

These findings support routine MMR testing in young colorectal cancer patients, consistent with universal testing approaches.

Who should care

Radiation OncologyMedical OncologyGynaecological OncologySurgical Oncology

Limitations

Retrospective single-center study; family history documentation may be incomplete and germline testing was not described.

Young colorectal cancer patients are more likely to have mismatch repair-deficient tumors, so test them.

This is an AI-generated summary of the published abstract, not a clinical recommendation. It may not reflect the full text or subsequent updates — verify against the original source before acting on it.

Abstract

Early-onset colorectal cancer (EOCRC), defined as colorectal cancer diagnosed before the age of 50 years, is increasing worldwide, with a similar trend emerging in China. However, the clinicopathological and mismatch repair features of EOCRC in Chinese patients remain insufficiently characterized. We retrospectively reviewed 23,414 colorectal neoplasia cases diagnosed at West China Hospital between November 2008 and June 2023. Among these, 4,159 colorectal cancer cases with complete immunohistochemical assessment of MLH1, PMS2, MSH2, and MSH6 were included in the primary analysis. Clinicopathological characteristics and mismatch repair status were compared between EOCRC and late-onset colorectal cancer (LOCRC), with additional stratification by documented family history. Multivariable logistic regression was used to evaluate the independent association between early-onset status and deficient mismatch repair (dMMR). Compared with LOCRC, EOCRC showed less favorable clinicopathological features, including higher proportions of poor differentiation, T4 tumors, nodal involvement, and advanced TNM stage. EOCRC also had a significantly higher prevalence of dMMR. In multivariable analysis, early-onset status was independently associated with dMMR in the overall cohort (adjusted OR, 2.27; 95% CI, 1.60-3.22; p < 0.001), and among patients without documented family history (adjusted OR, 1.95; 95% CI, 1.33-2.86; p < 0.001). Patterns of MMR protein loss differed according to documented family history status. In conclusion, EOCRC in this Chinese MMR-tested cohort was associated with more advanced clinicopathological features and a higher prevalence of dMMR, supporting routine MMR assessment in young patients with colorectal cancer.

DOI

10.1002/ijc.70667

PMID

42538607

Research metadata (titles, abstracts, authors, publication dates) is sourced from Europe PMC, which aggregates content from PubMed/MEDLINE, PubMed Central, and other providers under the U.S. National Library of Medicine (NLM/NCBI). NLM does not claim copyright on abstracts; the original journal publishers or authors may hold rights to the full articles. AI-generated summaries are derived only from the abstract, never the full text, and are always labeled as AI-generated.

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