Development and validation of a nomogram based on tumor margin irregularity and alpha-fetoprotein for predicting microvascular invasion in hepatocellular carcinoma - Summary - MDSpire

Development and validation of a nomogram based on tumor margin irregularity and alpha-fetoprotein for predicting microvascular invasion in hepatocellular carcinoma

  • By

  • Xiang Huang

  • Xiaofeng Chen

  • Xiangguang Chen

  • Ruibin Huang

  • Zhuozhi Dai

  • Ruyao Zhuang

  • Zhiqi Yang

  • June 26, 2026

  • 0 min

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Objective:

To develop and externally validate a preoperative nomogram based on tumor margin irregularity and alpha-fetoprotein (AFP) positivity for predicting microvascular invasion (MVI) in hepatocellular carcinoma (HCC).

Approach:
  • Study Design: Retrospective multicenter study with a training cohort of 487 patients and an external validation cohort of 256 patients.
  • Data Collection: Demographic, clinical, tumor-related, serological, and preoperative CT variables were compared by MVI status.
  • Analysis Method: LASSO regression for predictor selection followed by multivariable logistic regression; model performance assessed using ROC curves, AUC, calibration, and DCA.
Key Findings:
  • MVI was present in 187 of 487 patients in the training cohort and 95 of 256 patients in the validation cohort.
  • LASSO selected AFP positivity, irregular tumor margins, capsular interruption, and intratumoral hyperplastic vessels as predictors.
  • Irregular tumor margins (adjusted OR = 5.275, 95% CI: 3.165–8.791, p < 0.001) and AFP positivity (adjusted OR = 3.297, 95% CI: 1.983–5.481, p < 0.001) were identified as independent predictors.
  • The final model achieved AUCs of 0.740 and 0.781 in the training and validation cohorts, respectively.
Interpretation:

The nomogram based on tumor margin irregularity and AFP positivity showed fair-to-acceptable discrimination for preoperative MVI risk stratification in HCC patients.

Limitations:
  • The study is retrospective and may have selection bias.
  • External validation was limited to a single cohort.
  • The model requires further prospective multicenter validation.
Conclusion:

The nomogram may support exploratory preoperative MVI risk stratification in surgically treated or resectable HCC patients.

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