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Long-Term Follow-Up of Chronic Hepatitis C Patients Treated with Interferon-Alpha: Risk of Cirrhosis and Hepatocellular Carcinoma in a Single Center over 10 Years

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dc.contributor.authorLee, Hyun Jung-
dc.contributor.authorYeon, Jong Eun-
dc.contributor.authorYoon, Eileen L.-
dc.contributor.authorSuh, Sang Jun-
dc.contributor.authorKang, Keunhee-
dc.contributor.authorKim, Hae Rim-
dc.contributor.authorKang, Seong Hee-
dc.contributor.authorYoo, Yang Jae-
dc.contributor.authorJe, Jihye-
dc.contributor.authorKim, Ji Hoon-
dc.contributor.authorSeo, Yeon Seok-
dc.contributor.authorYim, Hyung Joon-
dc.contributor.authorByun, Kwan Soo-
dc.date.accessioned2021-09-05T01:07:06Z-
dc.date.available2021-09-05T01:07:06Z-
dc.date.created2021-06-15-
dc.date.issued2015-
dc.identifier.issn0300-5526-
dc.identifier.urihttps://scholar.korea.ac.kr/handle/2021.sw.korea/96285-
dc.description.abstractObjectives: Interferon (IFN)-based therapy for chronic hepatitis C (CHC) is cost-effective and is associated with reduced risk of disease progression. We aimed to assess the incidence of cirrhosis and hepatocellular carcinoma (HCC) and to identify risk factors associated with disease progression. Methods: We retrospectively reviewed 280 CHC patients who were registered at our hospital between 2001 and 2010. Results: About 80% of patients received antiviral treatment. The 10-year cumulative incidence of cirrhosis was significantly lower among patients who received antiviral therapy than among those who did not (8.3 vs. 44.0%; p = 0.001). Among them, patients with sustained virological response (SVR) had a significantly lower incidence of cirrhosis than those without SVR (0.6 vs. 33.9%; p < 0.001). Cox proportional hazards regression showed that SVR was the significant independent factor for reducing the risk of cirrhosis (hazard ratio, HR = 0.03; p = 0.034). The 10-year cumulative incidence of HCC was higher among patients who did not receive antiviral therapy than among those who did (43.9 vs. 6.1%; p < 0.001). Multivariate analysis showed that underlying cirrhosis was the only independent risk factor associated with HCC development (HR = 7.70; p = 0.010). Conclusions: SVR secondary to IFN-based therapy could reduce cirrhosis development in CHC patients. Underlying cirrhosis was the strongest predictor of HCC development. (C) 2015 S. Karger AG, Basel-
dc.languageEnglish-
dc.language.isoen-
dc.publisherKARGER-
dc.subjectSUSTAINED VIROLOGICAL RESPONSE-
dc.subjectVIRUS-INFECTION-
dc.subjectANTIVIRAL THERAPY-
dc.subjectPLUS RIBAVIRIN-
dc.subjectLIVER-DISEASE-
dc.subjectEND-POINTS-
dc.subjectMULTICENTER-
dc.subjectPROGRESSION-
dc.subjectFIBROSIS-
dc.subjectCOHORT-
dc.titleLong-Term Follow-Up of Chronic Hepatitis C Patients Treated with Interferon-Alpha: Risk of Cirrhosis and Hepatocellular Carcinoma in a Single Center over 10 Years-
dc.typeArticle-
dc.contributor.affiliatedAuthorYeon, Jong Eun-
dc.contributor.affiliatedAuthorKim, Ji Hoon-
dc.contributor.affiliatedAuthorSeo, Yeon Seok-
dc.contributor.affiliatedAuthorYim, Hyung Joon-
dc.contributor.affiliatedAuthorByun, Kwan Soo-
dc.identifier.doi10.1159/000369206-
dc.identifier.scopusid2-s2.0-84921357817-
dc.identifier.wosid000350267400003-
dc.identifier.bibliographicCitationINTERVIROLOGY, v.58, no.1, pp.14 - 21-
dc.relation.isPartOfINTERVIROLOGY-
dc.citation.titleINTERVIROLOGY-
dc.citation.volume58-
dc.citation.number1-
dc.citation.startPage14-
dc.citation.endPage21-
dc.type.rimsART-
dc.type.docTypeArticle-
dc.description.journalClass1-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.relation.journalResearchAreaVirology-
dc.relation.journalWebOfScienceCategoryVirology-
dc.subject.keywordPlusSUSTAINED VIROLOGICAL RESPONSE-
dc.subject.keywordPlusVIRUS-INFECTION-
dc.subject.keywordPlusANTIVIRAL THERAPY-
dc.subject.keywordPlusPLUS RIBAVIRIN-
dc.subject.keywordPlusLIVER-DISEASE-
dc.subject.keywordPlusEND-POINTS-
dc.subject.keywordPlusMULTICENTER-
dc.subject.keywordPlusPROGRESSION-
dc.subject.keywordPlusFIBROSIS-
dc.subject.keywordPlusCOHORT-
dc.subject.keywordAuthorChronic hepatitis C-
dc.subject.keywordAuthorCirrhosis-
dc.subject.keywordAuthorHepatocellular carcinoma-
dc.subject.keywordAuthorInterferon-
dc.subject.keywordAuthorSustained virological response-
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