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Predictive value of computed tomography radiomics for lymphatic-vascular space infiltration in colon cancer.

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American journal of cancer research 📖 저널 OA 100% 2022: 5/5 OA 2023: 7/7 OA 2024: 26/26 OA 2025: 71/71 OA 2026: 39/39 OA 2022~2026 2026 Vol.16(3) p. 1042-1055 OA
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Lv J, Yu H

📝 환자 설명용 한 줄

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) radiomi

🔬 핵심 임상 통계 (초록에서 자동 추출 — 원문 검증 권장)
  • 표본수 (n) 92
  • p-value P<0.05
  • p-value P<0.001
  • 95% CI 0.86-0.94

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↓ .bib ↓ .ris
APA Lv J, Yu H (2026). Predictive value of computed tomography radiomics for lymphatic-vascular space infiltration in colon cancer.. American journal of cancer research, 16(3), 1042-1055. https://doi.org/10.62347/AFQS4886
MLA Lv J, et al.. "Predictive value of computed tomography radiomics for lymphatic-vascular space infiltration in colon cancer.." American journal of cancer research, vol. 16, no. 3, 2026, pp. 1042-1055.
PMID 42004073 ↗
DOI 10.62347/AFQS4886

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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