A machine learning model for predicting hepatocellular carcinoma risk in patients with chronic hepatitis B

Author:

Lee Hye Won123ORCID,Kim Hwiyoung45,Park Taeyun5,Park Soo Young6,Chon Young Eun7,Seo Yeon Seok8ORCID,Lee Jae Seung123ORCID,park Jun Yong123ORCID,Kim Do Young123ORCID,Ahn Sang Hoon123ORCID,Kim Beom Kyung123ORCID,Kim Seung Up123ORCID

Affiliation:

1. Department of Internal Medicine Yonsei University College of Medicine Seoul Republic of Korea

2. Institute of Gastroenterology Yonsei University College of Medicine Seoul Republic of Korea

3. Yonsei Liver Center Severance Hospital Seoul Republic of Korea

4. Department of Biomedical Systems Informatics, Center for Clinical Imaging Data Science (CCIDS) Yonsei University College of Medicine Seoul Republic of Korea

5. Department of Artificial Intelligence Yonsei University, College of Medicine Seoul Republic of Korea

6. Department of Internal medicine Kyungpook National University School of Medicine Daegu Republic of Korea

7. Department of Internal Medicine CHA Bundang Medical Center, CHA University Bundang Republic of Korea

8. Department of Internal Medicine Korea University College of Medicine Seoul Republic of Korea

Abstract

AbstractBackgroundMachine learning (ML) algorithms can be used to overcome the prognostic performance limitations of conventional hepatocellular carcinoma (HCC) risk models. We established and validated an ML‐based HCC predictive model optimized for patients with chronic hepatitis B (CHB) infections receiving antiviral therapy (AVT).MethodsTreatment‐naïve CHB patients who were started entecavir (ETV) or tenofovir disoproxil fumarate (TDF) were enrolled. We used a training cohort (n = 960) to develop a novel ML model that predicted HCC development within 5 years and validated the model using an independent external cohort (n = 1937). ML algorithms consider all potential interactions and do not use predefined hypotheses.ResultsThe mean age of the patients in the training cohort was 48 years, and most patients (68.9%) were men. During the median 59.3 (interquartile range 45.8–72.3) months of follow‐up, 69 (7.2%) patients developed HCC. Our ML‐based HCC risk prediction model had an area under the receiver‐operating characteristic curve (AUC) of 0.900, which was better than the AUCs of CAMD (0.778) and REAL B (0.772) (both p < .05). The better performance of our model was maintained (AUC = 0.872 vs. 0.788 for CAMD and 0.801 for REAL B) in the validation cohort. Using cut‐off probabilities of 0.3 and 0.5, the cumulative incidence of HCC development differed significantly among the three risk groups (p < .001).ConclusionsOur new ML model performed better than models in terms of predicting the risk of HCC development in CHB patients receiving AVT.

Funder

National Research Foundation of Korea

Publisher

Wiley

Subject

Hepatology

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