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

Authors
Lee, Hye WonKim, HwiyoungPark, TaeyunPark, Soo YoungChon, Young EunSeo, Yeon SeokLee, Jae SeungPark, Jun YongKim, Do YoungAhn, Sang HoonKim, Beom KyungKim, Seung Up
Issue Date
Aug-2023
Publisher
Blackwell Publishing Inc.
Keywords
antiviral therapy; chronic hepatitis B; entecavir; hepatocellular carcinoma; machine learning; performance; prediction; prognosis; risk prediction; tenofovir
Citation
Liver International, v.43, no.8, pp 1813 - 1821
Pages
9
Indexed
SCIE
SCOPUS
Journal Title
Liver International
Volume
43
Number
8
Start Page
1813
End Page
1821
URI
https://scholarworks.korea.ac.kr/kumedicine/handle/2021.sw.kumedicine/64125
DOI
10.1111/liv.15597
ISSN
1478-3223
1478-3231
Abstract
Background Machine 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).Methods Treatment-naive 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.Results The 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).Conclusions Our new ML model performed better than models in terms of predicting the risk of HCC development in CHB patients receiving AVT.
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Seo, Yeon Seok
Anam Hospital (Department of Gastroenterology and Hepatology, Anam Hospital)
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