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Real-world Effectiveness and Safety of Direct-acting Antiviral Agents in Patients with Chronic Hepatitis C Genotype 2 Infection: Korean Multicenter Study

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dc.contributor.authorKang, Yeo Wool-
dc.contributor.authorBaek, Yang Hyun-
dc.contributor.authorLee, Sung Wook-
dc.contributor.authorPark, Sung-Jae-
dc.contributor.authorYoon, Jun Sik-
dc.contributor.authorYoon, Ki Tae-
dc.contributor.authorHong, Youngmi-
dc.contributor.authorHeo, Nae-Yun-
dc.contributor.authorSeo, Kwang Il-
dc.contributor.authorLee, Sang Soo-
dc.contributor.authorCho, Hyun Chin-
dc.contributor.authorShin, Jung Woo-
dc.date.accessioned2022-12-26T10:16:18Z-
dc.date.available2022-12-26T10:16:18Z-
dc.date.issued2021-05-31-
dc.identifier.issn1011-8934-
dc.identifier.issn1598-6357-
dc.identifier.urihttps://scholarworks.gnu.ac.kr/handle/sw.gnu/3689-
dc.description.abstractBackground: The advancement of treatment with direct-acting antiviral (DAA) agents has improved the cure rate of hepatitis C virus (HCV) infection close to 100%. The aim of our study was to assess the real-world effectiveness and safety of DAA regimens for the treatment of patients with chronic HCV genotype 2. Methods: We retrospectively analyzed the clinical data of patients treated with sofosbuvir plus ribavirin (SOF + RBV) or glecaprevir/pibrentasvir (G/P) for chronic HCV genotype 2 infection at seven university hospitals in the Korean southeast region. Results: SOF + RBV therapy produced an 89% and 98.3% sustained virologic response 12 week (SVR12) after treatment completion in the full analysis set and per-protocol set, respectively, and the corresponding values for G/P therapy were 89.5% and 99.2%, respectively. The difference between the treatments was probably because 6.2% (59/953) of patients in the SOF + RBV group did not complete the treatment and 9.8% (14/143) in the G/P group did not test HCV RNA after treatment completion. Adverse events (A/Es) were reported in 59.7% (569/953) and 25.9% (37/143) of the SOF + RBV and G/P groups, respectively. In the SOF + RBV group, 12 (1.26%) patients discontinued treatment owing to A/Es, whereas no patients discontinued treatment because of A/Es in the G/P group. Conclusion: In both treatment groups, SVR was high when treatment was completed. However, there was a high dropout rate in the SOF + RBV group, and the dropout analysis showed that these were patients with liver cirrhosis (LC; 43/285, 15.1%), especially those with decompensated LC (12/32, 37.5%). Therefore, an early initiation of antiviral therapy is recommended for a successful outcome before liver function declines. Furthermore, patients with decompensated LC who are considered candidates for SOF + RBV treatment should be carefully monitored to ensure that their treatment is completed, especially those with low hemoglobin and high alanine transaminase.-
dc.format.extent11-
dc.language영어-
dc.language.isoENG-
dc.publisher대한의학회-
dc.titleReal-world Effectiveness and Safety of Direct-acting Antiviral Agents in Patients with Chronic Hepatitis C Genotype 2 Infection: Korean Multicenter Study-
dc.title.alternativeReal-world Effectiveness and Safety of Direct-acting Antiviral Agents in Patients with Chronic Hepatitis C Genotype 2 Infection: Korean Multicenter Study-
dc.typeArticle-
dc.publisher.location대한민국-
dc.identifier.doi10.3346/jkms.2021.36.e142-
dc.identifier.scopusid2-s2.0-85107455262-
dc.identifier.wosid000657483000003-
dc.identifier.bibliographicCitationJournal of Korean Medical Science, v.36, no.21, pp 1 - 11-
dc.citation.titleJournal of Korean Medical Science-
dc.citation.volume36-
dc.citation.number21-
dc.citation.startPage1-
dc.citation.endPage11-
dc.type.docTypeArticle-
dc.identifier.kciidART002721887-
dc.description.isOpenAccessY-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.description.journalRegisteredClasskci-
dc.relation.journalResearchAreaGeneral & Internal Medicine-
dc.relation.journalWebOfScienceCategoryMedicine, General & Internal-
dc.subject.keywordPlusSOFOSBUVIR PLUS RIBAVIRIN-
dc.subject.keywordPlusVIRUS-INFECTION-
dc.subject.keywordPlusHEPATOCELLULAR-CARCINOMA-
dc.subject.keywordPlusOPEN-LABEL-
dc.subject.keywordPlusTHERAPY-
dc.subject.keywordPlusPIBRENTASVIR-
dc.subject.keywordPlusGLECAPREVIR-
dc.subject.keywordPlusVELPATASVIR-
dc.subject.keywordAuthorChronic Hepatitis C-
dc.subject.keywordAuthorDirect-acting Antiviral-
dc.subject.keywordAuthorEffectiveness-
dc.subject.keywordAuthorSafety-
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