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CAGE-B and SAGE-B models better predict the hepatitis B virus-related hepatocellular carcinoma after 5-year entecavir treatment than PAGE-B

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dc.contributor.authorChon, Hye Yeon-
dc.contributor.authorLee, Han Ah-
dc.contributor.authorPark, Soo Young-
dc.contributor.authorSeo, Yeon Seok-
dc.contributor.authorKim, Sang Gyune-
dc.contributor.authorLee, Chang Hun-
dc.contributor.authorLee, Tae Hee-
dc.contributor.authorAhn, Sang Hoon-
dc.contributor.authorWong, Vincent Wai-Sun-
dc.contributor.authorYip, Terry Cheuk-Fung-
dc.contributor.authorLiang, Lilian Yan-
dc.contributor.authorKim, In Hee-
dc.contributor.authorWong, Grace Lai-Hung-
dc.contributor.authorKim, Seung Up-
dc.date.accessioned2023-08-09T07:01:01Z-
dc.date.available2023-08-09T07:01:01Z-
dc.date.created2023-11-02-
dc.date.issued2023-02-
dc.identifier.issn1751-2972-
dc.identifier.urihttps://ir.ymlib.yonsei.ac.kr/handle/22282913/196031-
dc.description.abstractObjectives: The PAGE-B model consists of variables at the initiation of antiviral therapy (AVT), whereas the SAGE-B and CAGE-B models consist of variables after 5 years of AVT. We aimed to compare the predictive accuracy of three risk prediction models for hepatocellular carcinoma (HCC) development after 5 years of AVT in patients with chronic hepatitis B (CHB). Methods: A total of 1335 patients who initiated entecavir (ETV) treatment between 2006 and 2011 and were followed up for more than 5 years were enrolled in the study. Results: At ETV initiation, the median age was 49 years and the median score of the PAGE-B model was 14. After 5 years of ETV treatment, the median SAGE-B and CAGE-B scores were 6 and 6. During the study period, 93 (7.0%) patients developed HCC after 5-year treatment. In multivariate analysis, PAGE-B (hazard ratio [HR] 1.151, 95% confidence interval [CI] 1.087-1.219), SAGE-B (HR 1.340, 95% CI 1.2281.463), and CAGE-B (HR 1.327, 95% CI 1.223-1.440) models independently predicted HCC development after 5 years of treatment (all P < 0.001). The high-risk groups of the three risk prediction models showed a significantly higher risk of HCC development compared to the medium- and low-risk groups (both P < 0.05). The AUROC of the SAGE-B (0.772-0.844) and CAGE-B (0.785-0.838) models was significantly higher than those of the PAGE-B model (0.696-0.745) in predicting HCC development after 5 years of treatment (both P < 0.05). Conclusion: The SAGE-B and CAGE-B models might be better than the PAGE-B model in predicting HCC development after 5 years of ETV treatment.-
dc.description.statementOfResponsibilityrestriction-
dc.languageEnglish-
dc.publisherBlackwell Pub. Asia-
dc.relation.isPartOfJOURNAL OF DIGESTIVE DISEASES-
dc.relation.isPartOfJOURNAL OF DIGESTIVE DISEASES-
dc.rightsCC BY-NC-ND 2.0 KR-
dc.titleCAGE-B and SAGE-B models better predict the hepatitis B virus-related hepatocellular carcinoma after 5-year entecavir treatment than PAGE-B-
dc.typeArticle-
dc.contributor.collegeCollege of Medicine (의과대학)-
dc.contributor.departmentDept. of Internal Medicine (내과학교실)-
dc.contributor.googleauthorChon, Hye Yeon-
dc.contributor.googleauthorLee, Han Ah-
dc.contributor.googleauthorPark, Soo Young-
dc.contributor.googleauthorSeo, Yeon Seok-
dc.contributor.googleauthorKim, Sang Gyune-
dc.contributor.googleauthorLee, Chang Hun-
dc.contributor.googleauthorLee, Tae Hee-
dc.contributor.googleauthorAhn, Sang Hoon-
dc.contributor.googleauthorWong, Vincent Wai-Sun-
dc.contributor.googleauthorYip, Terry Cheuk-Fung-
dc.contributor.googleauthorLiang, Lilian Yan-
dc.contributor.googleauthorKim, In Hee-
dc.contributor.googleauthorWong, Grace Lai-Hung-
dc.contributor.googleauthorKim, Seung Up-
dc.identifier.doi10.1111/1751-2980.13172-
dc.relation.journalcodeJ03012-
dc.identifier.eissn1751-2980-
dc.identifier.pmid37057685-
dc.subject.keywordCAGE-B-
dc.subject.keywordhepatitis B-
dc.subject.keywordPAGE-B-
dc.subject.keywordrisk prediction-
dc.subject.keywordSAGE-B-
dc.contributor.alternativeNameKim, Seung Up-
dc.contributor.affiliatedAuthorChon, Hye Yeon-
dc.contributor.affiliatedAuthorAhn, Sang Hoon-
dc.contributor.affiliatedAuthorKim, Seung Up-
dc.identifier.scopusid2-s2.0-85158996097-
dc.identifier.wosid000985654700001-
dc.citation.volume24-
dc.citation.number2-
dc.citation.startPage113-
dc.citation.endPage121-
dc.identifier.bibliographicCitationJOURNAL OF DIGESTIVE DISEASES, Vol.24(2) : 113-121, 2023-02-
dc.identifier.rimsid81065-
dc.type.rimsART-
dc.description.journalClass1-
dc.description.journalClass1-
dc.subject.keywordAuthorCAGE-B-
dc.subject.keywordAuthorhepatitis B-
dc.subject.keywordAuthorPAGE-B-
dc.subject.keywordAuthorrisk prediction-
dc.subject.keywordAuthorSAGE-B-
dc.subject.keywordPlusCLINICAL-PRACTICE GUIDELINES-
dc.subject.keywordPlusRISK-
dc.subject.keywordPlusCAUCASIANS-
dc.subject.keywordPlusMANAGEMENT-
dc.subject.keywordPlusTENOFOVIR-
dc.subject.keywordPlusTHERAPY-
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

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