Evidence map›Paper›PMID 42538596›Full record

ArticleCancer medicine2026

Tertiary Lymphoid Structures as Predictors of Recurrence in Colorectal Cancer: Development and Validation of a Machine Learning-Based Scoring Model.

Xian-Hua Lei, Rong Li, Dong-Mei Wang, Li Liu, Zhi-Qiang Wang, Hui-Juan Li

Abstract readValidation Study
In one paragraph

Article in Cancer medicine, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

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1citing papers in PubMed
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3 · Its place in the literature

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1 citing paper in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

6 authors.

Xian-Hua LeiDepartment of Pathology, Ganzhou Cancer Hospital, The Affiliated Cancer Hospital of Gannan Medical University, Ganzhou, Jiangxi, China.
Rong LiDepartment of Pathology, Ganzhou Cancer Hospital, The Affiliated Cancer Hospital of Gannan Medical University, Ganzhou, Jiangxi, China.
Dong-Mei WangDepartment of Pathology, Ganzhou Cancer Hospital, The Affiliated Cancer Hospital of Gannan Medical University, Ganzhou, Jiangxi, China.
Li LiuDepartment of Pathology, Ganzhou Cancer Hospital, The Affiliated Cancer Hospital of Gannan Medical University, Ganzhou, Jiangxi, China.
Zhi-Qiang WangDepartment of Pathology, Ganzhou Cancer Hospital, The Affiliated Cancer Hospital of Gannan Medical University, Ganzhou, Jiangxi, China.
Hui-Juan LiDepartment of Pathology, Ganzhou Cancer Hospital, The Affiliated Cancer Hospital of Gannan Medical University, Ganzhou, Jiangxi, China.ORCID https://orcid.org/0009-0000-2839-2761

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundTertiary lymphoid structures (TLS) are prognostic immune aggregates in the tumor microenvironment, but the value of location-specific TLS features for predicting colorectal cancer (CRC) recurrence remains unclear. This study developed and internally validated a machine-learning (ML) model integrating TLS features for recurrence prediction in stage II-III CRC.

methodsWe retrospectively included 224 patients with stage II-III CRC after curative resection and split them into training (n = 156) and held-out internal validation (n = 68) cohorts. TLS at intratumoral, invasive-front, and peritumoral sites were semi-quantitatively scored by two blinded pathologists. LASSO selected predictors from 39 candidate variables. Five ML algorithms were trained with stratified cross-validation, predefined tuning, and training-only preprocessing. Performance was evaluated using discrimination, calibration, decision-curve/clinical-impact analyses, reclassification indices, SHAP interpretation, and Kaplan-Meier risk stratification.

resultsRecurrence occurred in 89 patients (39.7%). LASSO retained peritumoral TLS score, invasive-front TLS score, and preoperative CEA. TLS scoring showed high interobserver agreement (weighted kappa: 0.82-0.86). LightGBM provided the most balanced performance, with AUCs of 0.872 (95% CI: 0.814-0.923) in training and 0.718 (95% CI: 0.572-0.839) in internal validation. SHAP ranked invasive-front TLS score as the most influential predictor. The Youden cutoff (0.5017) separated high- and low-risk groups with significantly different disease-free survival (log-rank p < 0.0001; hazard ratio = 5.132, 95% CI: 3.263-8.073). In exploratory comparison, validation AUCs were 0.727 for TLS-only, 0.542 for clinical-only, and 0.737 for combined models.

conclusionsA TLS-based ML model showed moderate internal validation performance for CRC recurrence prediction. Location-specific TLS features may support postoperative risk stratification, but external multicenter and molecularly integrated validation is required before clinical use.

Indexed as

Colorectal NeoplasmsMachine LearningNeoplasm Recurrence, LocalTertiary Lymphoid StructuresAgedClassification AlgorithmsFemaleHumansMaleMiddle AgedNeoplasm StagingPredictive Learning ModelsPrognosisRetrospective StudiesTumor Microenvironmentcolorectal cancermachine learningrecurrence predictiontertiary lymphoid structures

Identifiers

PMID42538596
PMCPMC13428042

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