ArticleAmerican journal of cancer research2026
Predictive value of computed tomography radiomics for lymphatic-vascular space infiltration in colon cancer.
Article in American journal of cancer research, 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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Abstract
This study aimed to construct and validate a preoperative predictive model for lymphatic-vascular space infiltration (LVSI) in colon cancer using clinical features and computed tomography (CT) radiomics, and to evaluate its clinical utility. A total of 244 colon cancer patients treated at Yongkang First People's Hospital from January 2018 to January 2024 were enrolled as the training set (LVSI-positive: n=92, LVSI-negative: n=152), and 58 patients treated between February 2024 and August 2025 served as the validation set. Clinical data were collected, and contrast-enhanced CT images were analyzed. Radiomic features were extracted using PyRadiomics, and features with intraclass correlation coefficient (ICC) >0.8 were retained to ensure reproducibility, and least absolute shrinkage and selection operator (LASSO) regression was applied for dimensionality reduction. A clinical model, a radiomics model (based on Rad-score), and a combined model were established via multivariate logistic regression. Receiver operating characteristic (ROC) curve, calibration curve, Hosmer-Lemeshow test, and decision curve analysis (DCA) were used to assess model performance. The results showed that tumor diameter, differentiation degree, CT-detected extramural vascular invasion (cEMVI), and carcinoembryonic antigen (CEA) were independent risk factors for LVSI (all P<0.05). Four key radiomic features were screened to calculate Rad-score. In the training set, the combined model achieved an area under the curve (AUC) of 0.90 (95% CI: 0.86-0.94), significantly higher than the clinical model (AUC=0.75) and radiomics model (AUC=0.84) (both P<0.001), with accuracy, sensitivity, and specificity of 0.82, 0.80, and 0.86, respectively. In the validation set, the combined model maintained an AUC of 0.92 (95% CI: 0.86-0.99), outperforming the clinical model (AUC=0.71, P=0.004), and showed good calibration (Hosmer-Lemeshow P=0.364) and positive net benefits in DCA. The combined model integrating clinical features and CT radiomics exhibits excellent performance in preoperative prediction of LVSI in colon cancer, providing a reliable tool for individualized treatment decision-making.
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