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Hepatitis C Virus Cure Rates Are Reduced in Patients With Active but Not Inactive Hepatocellular Carcinoma: A Practice Implication

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dc.contributor.authorOgawa, Eiichi-
dc.contributor.authorToyoda, Hidenori-
dc.contributor.authorIio, Etsuko-
dc.contributor.authorJun, Dae Won-
dc.contributor.authorHuang, Chung-Feng-
dc.contributor.authorEnomoto, Masaru-
dc.contributor.authorHsu, Yao-Chun-
dc.contributor.authorHaga, Hiroaki-
dc.contributor.authorIwane, Shinji-
dc.contributor.authorWong, Grace-
dc.contributor.authorLee, Dong Hyun-
dc.contributor.authorTada, Toshifumi-
dc.contributor.authorLiu, Chen-Hua-
dc.contributor.authorChuang, Wan-Long-
dc.contributor.authorHayashi, Jun-
dc.contributor.authorCheung, Ramsey-
dc.contributor.authorYasuda, Satoshi-
dc.contributor.authorTseng, Cheng-Hao-
dc.contributor.authorTakahashi, Hirokazu-
dc.contributor.authorTran, Sally-
dc.contributor.authorYeo, Yee Hui-
dc.contributor.authorHenry, Linda-
dc.contributor.authorBarnett, Scott D.-
dc.contributor.authorNomura, Hideyuki-
dc.contributor.authorNakamuta, Makoto-
dc.contributor.authorDai, Chia-Yen-
dc.contributor.authorHuang, Jee-Fu-
dc.contributor.authorYang, Hwai-, I-
dc.contributor.authorLee, Mei-Hsuan-
dc.contributor.authorJun, Mi Jung-
dc.contributor.authorKao, Jia-Horng-
dc.contributor.authorEguchi, Yuichiro-
dc.contributor.authorUeno, Yoshiyuki-
dc.contributor.authorTamori, Akihiro-
dc.contributor.authorFurusyo, Norihiro-
dc.contributor.authorYu, Ming-Lung-
dc.contributor.authorTanaka, Yasuhito-
dc.contributor.authorNguyen, Mindie H.-
dc.date.accessioned2021-08-02T08:28:33Z-
dc.date.available2021-08-02T08:28:33Z-
dc.date.created2021-05-12-
dc.date.issued2020-12-
dc.identifier.issn1058-4838-
dc.identifier.urihttps://scholarworks.bwise.kr/hanyang/handle/2021.sw.hanyang/8165-
dc.description.abstractBackground. Cure rates of hepatitis C virus (HCV) treatment with direct-acting antivirals (DAAs) for patients with active and inactive hepatocellular carcinoma (HCC) may differ, but well-controlled studies are limited. We aimed to evaluate DAA outcomes in a large East Asian HCV/HCC population compared with HCV/non-HCC patients. Methods. Using data from the Real-World Evidence from the Asia Liver Consortium (REAL-C) registry (Hong Kong, Japan, South Korea, and Taiwan), we used propensity score matching (PSM) to match HCC and non-HCC (1:1) groups for age, sex, cirrhosis, prior treatment, HCV genotype, treatment regimen, baseline platelet count, HCV RNA, total bilirubin, alanine aminotransferase, and albumin levels to evaluate DAA treatment outcomes in a large population of HCV/HCC compared with HCV/non-HCC patients. Results. We included 6081 patients (HCC, n = 465; non-HCC, n = 5 616) treated with interferon-free DAAs. PSM of the entire study population yielded 436 matched pairs with similar baseline characteristics. There was no statistically significant difference in the overall SVR rate of HCC (92.7%) and non-HCC (95.0%) groups. Rates of treatment discontinuation, adverse effects, and death were also similar between HCC and non-HCC groups. Among patients with HCC, those with active HCC had a lower SVR than inactive HCC cases (85.5% vs 93.7%; P = .03). On multivariable analysis, active HCC, but not inactive HCC, was significantly associated with lower SVR (OR, 0.28; P = .01) when compared with non-HCC. Conclusions. Active HCC but not inactive HCC was independently associated with lower SVR compared with non-HCC patients undergoing DAA therapy, although cure rate was still relatively high (85%) in active HCC patients.-
dc.language영어-
dc.language.isoen-
dc.publisherOXFORD UNIV PRESS INC-
dc.titleHepatitis C Virus Cure Rates Are Reduced in Patients With Active but Not Inactive Hepatocellular Carcinoma: A Practice Implication-
dc.typeArticle-
dc.contributor.affiliatedAuthorJun, Dae Won-
dc.identifier.doi10.1093/cid/ciz1160-
dc.identifier.scopusid2-s2.0-85099326545-
dc.identifier.wosid000607829500013-
dc.identifier.bibliographicCitationCLINICAL INFECTIOUS DISEASES, v.71, no.11, pp.2840 - 2848-
dc.relation.isPartOfCLINICAL INFECTIOUS DISEASES-
dc.citation.titleCLINICAL INFECTIOUS DISEASES-
dc.citation.volume71-
dc.citation.number11-
dc.citation.startPage2840-
dc.citation.endPage2848-
dc.type.rimsART-
dc.type.docTypeArticle-
dc.description.journalClass1-
dc.description.isOpenAccessN-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.relation.journalResearchAreaImmunology-
dc.relation.journalResearchAreaInfectious Diseases-
dc.relation.journalResearchAreaMicrobiology-
dc.relation.journalWebOfScienceCategoryImmunology-
dc.relation.journalWebOfScienceCategoryInfectious Diseases-
dc.relation.journalWebOfScienceCategoryMicrobiology-
dc.subject.keywordPlusGENOTYPE DISTRIBUTION-
dc.subject.keywordPlusTHERAPY-
dc.subject.keywordPlusINFECTION-
dc.subject.keywordPlusANTIVIRALS-
dc.subject.keywordPlusOUTCOMES-
dc.subject.keywordAuthorhepatitis C virus-
dc.subject.keywordAuthorhepatocellular carcinoma-
dc.subject.keywordAuthordirect-acting antivirals-
dc.subject.keywordAuthorAsian-
dc.subject.keywordAuthorpropensity score matching-
dc.identifier.urlhttps://academic.oup.com/cid/article/71/11/2840/5645107-
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