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

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dc.contributor.authorLee, Hye Won-
dc.contributor.authorKim, Hwiyoung-
dc.contributor.authorPark, Taeyun-
dc.contributor.authorPark, Soo Young-
dc.contributor.authorChon, Young Eun-
dc.contributor.authorSeo, Yeon Seok-
dc.contributor.authorLee, Jae Seung-
dc.contributor.authorPark, Jun Yong-
dc.contributor.authorKim, Do Young-
dc.contributor.authorAhn, Sang Hoon-
dc.contributor.authorKim, Beom Kyung-
dc.contributor.authorKim, Seung Up-
dc.date.accessioned2023-11-28T03:00:37Z-
dc.date.available2023-11-28T03:00:37Z-
dc.date.created2024-01-18-
dc.date.issued2023-08-
dc.identifier.issn1478-3223-
dc.identifier.urihttps://ir.ymlib.yonsei.ac.kr/handle/22282913/196719-
dc.description.abstractBackground 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.-
dc.description.statementOfResponsibilityrestriction-
dc.languageEnglish-
dc.publisherWiley-Blackwell-
dc.relation.isPartOfLIVER INTERNATIONAL-
dc.relation.isPartOfLIVER INTERNATIONAL-
dc.rightsCC BY-NC-ND 2.0 KR-
dc.titleA machine learning model for predicting hepatocellular carcinoma risk in patients with chronic hepatitis B-
dc.typeArticle-
dc.contributor.collegeCollege of Medicine (의과대학)-
dc.contributor.departmentDept. of Internal Medicine (내과학교실)-
dc.contributor.googleauthorLee, Hye Won-
dc.contributor.googleauthorKim, Hwiyoung-
dc.contributor.googleauthorPark, Taeyun-
dc.contributor.googleauthorPark, Soo Young-
dc.contributor.googleauthorChon, Young Eun-
dc.contributor.googleauthorSeo, Yeon Seok-
dc.contributor.googleauthorLee, Jae Seung-
dc.contributor.googleauthorPark, Jun Yong-
dc.contributor.googleauthorKim, Do Young-
dc.contributor.googleauthorAhn, Sang Hoon-
dc.contributor.googleauthorKim, Beom Kyung-
dc.contributor.googleauthorKim, Seung Up-
dc.identifier.doi10.1111/liv.15597-
dc.relation.journalcodeJ02171-
dc.identifier.eissn1478-3231-
dc.identifier.pmid37452503-
dc.subject.keywordantiviral therapy-
dc.subject.keywordchronic hepatitis B-
dc.subject.keywordentecavir-
dc.subject.keywordhepatocellular carcinoma-
dc.subject.keywordmachine learning-
dc.subject.keywordperformance-
dc.subject.keywordprediction-
dc.subject.keywordprognosis-
dc.subject.keywordrisk prediction-
dc.subject.keywordtenofovir-
dc.contributor.alternativeNameKim, Do Young-
dc.contributor.affiliatedAuthorLee, Hye Won-
dc.contributor.affiliatedAuthorKim, Hwiyoung-
dc.contributor.affiliatedAuthorLee, Jae Seung-
dc.contributor.affiliatedAuthorPark, Jun Yong-
dc.contributor.affiliatedAuthorKim, Do Young-
dc.contributor.affiliatedAuthorAhn, Sang Hoon-
dc.contributor.affiliatedAuthorKim, Beom Kyung-
dc.contributor.affiliatedAuthorKim, Seung Up-
dc.identifier.scopusid2-s2.0-85164755969-
dc.identifier.wosid001063449000020-
dc.citation.volume43-
dc.citation.number8-
dc.citation.startPage1813-
dc.citation.endPage1821-
dc.identifier.bibliographicCitationLIVER INTERNATIONAL, Vol.43(8) : 1813-1821, 2023-08-
dc.identifier.rimsid81600-
dc.type.rimsART-
dc.description.journalClass1-
dc.description.journalClass1-
dc.subject.keywordAuthorantiviral therapy-
dc.subject.keywordAuthorchronic hepatitis B-
dc.subject.keywordAuthorentecavir-
dc.subject.keywordAuthorhepatocellular carcinoma-
dc.subject.keywordAuthormachine learning-
dc.subject.keywordAuthorperformance-
dc.subject.keywordAuthorprediction-
dc.subject.keywordAuthorprognosis-
dc.subject.keywordAuthorrisk prediction-
dc.subject.keywordAuthortenofovir-
dc.subject.keywordPlusORAL ANTIVIRAL TREATMENT-
dc.subject.keywordPlusNATURAL-HISTORY-
dc.subject.keywordPlusSCORING SYSTEM-
dc.subject.keywordPlusVIRUS-
dc.type.docTypeArticle-
dc.description.isOpenAccessN-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.relation.journalWebOfScienceCategoryGastroenterology & Hepatology-
dc.relation.journalResearchAreaGastroenterology & Hepatology-
Appears in Collections:
1. College of Medicine (의과대학) > Dept. of Internal Medicine (내과학교실) > 1. Journal Papers
1. College of Medicine (의과대학) > Dept. of Neurosurgery (신경외과학교실) > 1. Journal Papers

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