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Updated: Jul 6, 2026

Modeling Hepatitis B Virus Infection in Non-Hepatic 293T-NE-3NRs Cells
Published on: June 5, 2020
Machine learning models for predicting hepatocellular carcinoma development in patients with chronic viral hepatitis
Warissara Kuaaroon1, Thodsawit Tiyarattanachai1, Terapap Apiparakoon2
1Faculty of Medicine, Chulalongkorn University, Bangkok 10330, Thailand.
Background:
Chronic hepatitis B (CHB) infection is the major risk factor for hepatocellular carcinoma (HCC).
Objective:
To develop machine-learning models for predicting an individual risk of HCC development in CHB-infected patients.
Methods:
Machine learning models were constructed using features from follow-up visits of CHB patients to predict the diagnosis of HCC development within 6 months after each index follow-up. We developed 4 model variants using all features, with alpha fetoprotein (AFP) (AF ) and without AFP (AF ); and selected features, with AFP (SF ) and without AFP (SF ). Performance was evaluated using 10-fold cross-validation on a derivation cohort and further validated on an independent cohort.
Results:
In the derivation cohort of 2,382 patients, of whom 117 developed HCC, AF achieved higher sensitivity (0.634, 95% confidence interval [CI]: 0.559-0.708) and specificity (0.836; 0.830-0.842) than AF (sensitivity 0.553; 0.476-0.630 and specificity 0.786; 0.779-0.792). SF also achieved higher sensitivity (0.683; 0.611-0.755 vs. 0.658; 0.585-0.732) and specificity (0.756; 0.749-0.763 vs. 0.744; 0.737-0.751) than SF . Performance of SF and SF were tested in another cohort of 162 patients in which 57 patients developed HCC. SF achieved sensitivity and specificity of 0.634 (0.522-0.746) and 0.657 (0.615-0.699), while sensitivity and specificity of SF were 0.690 (0.583-0.798) and 0.651 (0.609-0.693), respectively.
Conclusion:
The machine learning models demonstrate good performance for predicting short-term risk for HCC development and may potentially be used for tailoring surveillance interval for CHB patients.
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