Real-world Effectiveness and Safety of Direct-acting Antiviral Agents in Patients with Chronic Hepatitis C Genotype 2 Infection: Korean Multicenter Study
DC Field | Value | Language |
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dc.contributor.author | Kang, Yeo Wool | - |
dc.contributor.author | Baek, Yang Hyun | - |
dc.contributor.author | Lee, Sung Wook | - |
dc.contributor.author | Park, Sung-Jae | - |
dc.contributor.author | Yoon, Jun Sik | - |
dc.contributor.author | Yoon, Ki Tae | - |
dc.contributor.author | Hong, Youngmi | - |
dc.contributor.author | Heo, Nae-Yun | - |
dc.contributor.author | Seo, Kwang Il | - |
dc.contributor.author | Lee, Sang Soo | - |
dc.contributor.author | Cho, Hyun Chin | - |
dc.contributor.author | Shin, Jung Woo | - |
dc.date.accessioned | 2022-12-26T10:16:18Z | - |
dc.date.available | 2022-12-26T10:16:18Z | - |
dc.date.issued | 2021-05-31 | - |
dc.identifier.issn | 1011-8934 | - |
dc.identifier.issn | 1598-6357 | - |
dc.identifier.uri | https://scholarworks.gnu.ac.kr/handle/sw.gnu/3689 | - |
dc.description.abstract | Background: 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.extent | 11 | - |
dc.language | 영어 | - |
dc.language.iso | ENG | - |
dc.publisher | 대한의학회 | - |
dc.title | Real-world Effectiveness and Safety of Direct-acting Antiviral Agents in Patients with Chronic Hepatitis C Genotype 2 Infection: Korean Multicenter Study | - |
dc.title.alternative | Real-world Effectiveness and Safety of Direct-acting Antiviral Agents in Patients with Chronic Hepatitis C Genotype 2 Infection: Korean Multicenter Study | - |
dc.type | Article | - |
dc.publisher.location | 대한민국 | - |
dc.identifier.doi | 10.3346/jkms.2021.36.e142 | - |
dc.identifier.scopusid | 2-s2.0-85107455262 | - |
dc.identifier.wosid | 000657483000003 | - |
dc.identifier.bibliographicCitation | Journal of Korean Medical Science, v.36, no.21, pp 1 - 11 | - |
dc.citation.title | Journal of Korean Medical Science | - |
dc.citation.volume | 36 | - |
dc.citation.number | 21 | - |
dc.citation.startPage | 1 | - |
dc.citation.endPage | 11 | - |
dc.type.docType | Article | - |
dc.identifier.kciid | ART002721887 | - |
dc.description.isOpenAccess | Y | - |
dc.description.journalRegisteredClass | scie | - |
dc.description.journalRegisteredClass | scopus | - |
dc.description.journalRegisteredClass | kci | - |
dc.relation.journalResearchArea | General & Internal Medicine | - |
dc.relation.journalWebOfScienceCategory | Medicine, General & Internal | - |
dc.subject.keywordPlus | SOFOSBUVIR PLUS RIBAVIRIN | - |
dc.subject.keywordPlus | VIRUS-INFECTION | - |
dc.subject.keywordPlus | HEPATOCELLULAR-CARCINOMA | - |
dc.subject.keywordPlus | OPEN-LABEL | - |
dc.subject.keywordPlus | THERAPY | - |
dc.subject.keywordPlus | PIBRENTASVIR | - |
dc.subject.keywordPlus | GLECAPREVIR | - |
dc.subject.keywordPlus | VELPATASVIR | - |
dc.subject.keywordAuthor | Chronic Hepatitis C | - |
dc.subject.keywordAuthor | Direct-acting Antiviral | - |
dc.subject.keywordAuthor | Effectiveness | - |
dc.subject.keywordAuthor | Safety | - |
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