Evidence map›Paper›PMID 42277735›Full record

ArticleBMC cancer2026

Clinical factors are more strongly associated with prognosis than genetic alterations in early-onset colorectal cancer: a retrospective cohort study.

Kien Trung Le, Huy Duc Tran, Minh Duc Do, Thinh Huu Nguyen, Tin Trung Nguyen, Trung Thien Tran

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Article in BMC 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.

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5 · Who and what money

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6 authors.

Kien Trung LeUniversity Medical Center HCMC, University of Medicine and Pharmacy, Ho Chi Minh City, Vietnam.
Huy Duc TranUniversity Medical Center HCMC, University of Medicine and Pharmacy, Ho Chi Minh City, Vietnam. huy.td@umc.edu.vn.
Minh Duc DoSchool of Medicine, University of Medicine and Pharmacy, Ho Chi Minh City, Vietnam.
Thinh Huu NguyenUniversity Medical Center HCMC, University of Medicine and Pharmacy, Ho Chi Minh City, Vietnam.
Tin Trung NguyenUniversity Medical Center HCMC, University of Medicine and Pharmacy, Ho Chi Minh City, Vietnam.
Trung Thien TranSchool of Medicine, University of Medicine and Pharmacy, Ho Chi Minh City, Vietnam.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundEarly-onset colorectal cancer (EOCRC) is increasing globally and exhibits both aggressive clinicopathological features and distinct molecular characteristics. However, the relative contribution of clinical and genetic factors to prognosis remains unclear, particularly in underrepresented populations.

methodsA retrospective cohort study was conducted on 100 colorectal cancer (CRC) patients under 50 years of age, diagnosed and treated between January 2016 and December 2020, with follow-up up to 60 months or until death. Patients were stratified by patient characteristics, oncological features, and genetic mutation status to perform overall survival (OS) analysis.

resultsThe mean OS was 49.8 months (95% CI: 46.4-53.2), with an estimated 5-year OS rate of 65.2%. The mean disease-free survival (DFS) was 50.1 months (95% CI: 46.2-53.9). In univariate analysis, factors significantly associated with OS included serum CEA level at diagnosis (p = 0.001), histological grade (p = 0.006), mode of surgery (emergency vs. elective) (p = 0.003), curative resection status (p < 0.001), disease stage (p < 0.001), mutations in the POL-MMR DNA repair gene group (p = 0.035), high mutation accumulation (p = 0.020), PIK3CA mutation (p = 0.036), and co-mutation of RAS/RAF and MMR genes (p = 0.011). However, when adjusted for disease stage, only patient and oncological factors remained associated with OS, including elevated CEA (HR = 2.33, 95% CI: 1.2-4.7, p = 0.018), poorly differentiated tumors (HR = 2.57, 95% CI: 1.2-5.7, p = 0.021), emergency surgery (HR = 3.50, 95% CI: 1.5-7.9, p = 0.003), and curative treatment (HR = 0.10, 95% CI: 0.05-0.2, p < 0.001).

conclusionIn EOCRC, clinical and treatment-related factors remained independently associated with overall survival after adjustment for disease stage, whereas the evaluated genetic variables did not retain statistical significance. These findings highlight the importance of clinical management strategies, while the prognostic value of genetic alterations requires further investigation.

Indexed as

Biomarkers, TumorColorectal NeoplasmsAdultAge of OnsetDisease-Free SurvivalFemaleHumansMaleMiddle AgedMutationNeoplasm StagingPrognosisRetrospective StudiesBiomarkers, TumorEarly-onset colorectal cancerGene mutationsLong-term outcomesVietnam

Identifiers

PMID42277735
PMCPMC13688740

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