https://scholars.lib.ntu.edu.tw/handle/123456789/581793
DC 欄位 | 值 | 語言 |
---|---|---|
dc.contributor.author | SHIH-JER HSU | en_US |
dc.contributor.author | Chiu M.-C. | en_US |
dc.contributor.author | YU-JEN FANG | en_US |
dc.contributor.author | Yang T.-H. | en_US |
dc.contributor.author | Yu J.-J. | en_US |
dc.contributor.author | CHIEH-CHANG CHEN | en_US |
dc.contributor.author | Kuo C.-C. | en_US |
dc.contributor.author | Lee J.-Y. | en_US |
dc.contributor.author | CHIEN-HUNG CHEN | en_US |
dc.contributor.author | DING-SHINN CHEN | en_US |
dc.contributor.author | JIA-HORNG KAO | en_US |
dc.date.accessioned | 2021-09-04T05:16:49Z | - |
dc.date.available | 2021-09-04T05:16:49Z | - |
dc.date.issued | 2019 | - |
dc.identifier.issn | 0929-6646 | - |
dc.identifier.uri | https://www.scopus.com/inward/record.uri?eid=2-s2.0-85068205798&doi=10.1016%2fj.jfma.2019.06.014&partnerID=40&md5=3326d5e95c2d9ea32fc8bf019ae3d73c | - |
dc.identifier.uri | https://scholars.lib.ntu.edu.tw/handle/123456789/581793 | - |
dc.description.abstract | Background: Glecaprevir/pibrentasvir (GLE/PIB) is a pangenotypic direct-acting antiviral agent for the treatment of chronic hepatitis C virus (HCV) infection. Real-world data of GLE/PIB in Asian patients other than Japanese are limited. We thus investigated the effectiveness and safety profile of GLE/PIB in Taiwanese patients with chronic hepatitis C (CHC). Methods: CHC patients who received 8, 12, or 16 weeks of GLE/PIB between August and October of 2018 were consecutively enrolled. The treatment duration was determined according to drug label. The hepatic fibrosis was staged according to liver histology, transient elastography, fibrosis index based on 4 factors (FIB-4), or findings of ultrasonography/endoscopy. The primary endpoint was sustained virological response at week 12 off therapy (SVR12). The safety profiles were also assessed. Results: A total of 110 CHC patients with 51% of males were enrolled. The median age was 70 years. A majority (82%) of patients were infected with HCV genotype 2. Forty-six (42%) and 64 (58%) patients had advanced hepatic fibrosis and compensated cirrhosis, respectively. Forty-five (41%) non-cirrhotic patients were treated for 8 weeks. The overall SVR12 rates were 100%, regardless of baseline clinical characteristics. The common adverse events (AEs) were pruritus (12%), anorexia (6%), and fatigue (5%). Nine (8%) serious AEs unrelated to GLE/PIB occurred. Three (2%) patients had Grade 3 elevation of total bilirubin level. None had premature treatment termination, hepatic decompensation, or death. Conclusion: Interferon-free GLE/PIB regimen is highly effective and safe for Asian chronic hepatitis C patients with advanced hepatic fibrosis or compensated cirrhosis. ? 2019 Formosan Medical Association | en_US |
dc.publisher | Elsevier B.V. | en_US |
dc.relation.ispartof | Journal of the Formosan Medical Association | en_US |
dc.subject.classification | [SDGs]SDG3 | - |
dc.subject.other | bilirubin; glecaprevir plus pibrentasvir; ABT-493; antivirus agent; benzimidazole derivative; pibrentasvir; quinoxaline derivative; sulfonamide; abdominal infection; adult; aged; anorexia; antiviral therapy; Article; Asian; bacteremia; chronic hepatitis C; cohort analysis; compensated liver cirrhosis; controlled study; drug efficacy; drug safety; echography; fatigue; female; femur fracture; gastrointestinal hemorrhage; human; liver fibrosis; liver histology; major clinical study; male; pruritus; retrospective study; salmonellosis; side effect; sustained virologic response; Taiwanese; transient elastography; treatment duration; unspecified side effect; chronic hepatitis C; combination drug therapy; drug effect; Hepacivirus; liver cirrhosis; middle aged; pathology; Taiwan; very elderly; virology; Adult; Aged; Aged, 80 and over; Antiviral Agents; Benzimidazoles; Drug Therapy, Combination; Female; Hepacivirus; Hepatitis C, Chronic; Humans; Liver Cirrhosis; Male; Middle Aged; Quinoxalines; Retrospective Studies; Sulfonamides; Sustained Virologic Response; Taiwan | - |
dc.title | Real-world effectiveness and safety of glecaprevir/pibrentasvir in Asian patients with chronic hepatitis C | en_US |
dc.type | journal article | en |
dc.identifier.doi | 10.1016/j.jfma.2019.06.014 | - |
dc.identifier.pmid | 31279502 | - |
dc.identifier.scopus | 2-s2.0-85068205798 | - |
dc.relation.pages | 1187-1192 | en_US |
dc.relation.journalvolume | 118 | en_US |
dc.relation.journalissue | 8 | en_US |
item.openairetype | journal article | - |
item.openairecristype | http://purl.org/coar/resource_type/c_6501 | - |
item.fulltext | no fulltext | - |
item.grantfulltext | none | - |
item.cerifentitytype | Publications | - |
crisitem.author.dept | Internal Medicine-NTUH | - |
crisitem.author.dept | Internal Medicine | - |
crisitem.author.dept | Internal Medicine-NTUHYL | - |
crisitem.author.dept | Internal Medicine | - |
crisitem.author.dept | Internal Medicine-NTUH | - |
crisitem.author.dept | Internal Medicine | - |
crisitem.author.dept | Internal Medicine-NTUH | - |
crisitem.author.dept | National Taiwan University Cancer Center (NTUCC) | - |
crisitem.author.dept | Internal Medicine-NTUH | - |
crisitem.author.dept | Clinical Medicine | - |
crisitem.author.dept | Internal Medicine-NTUH | - |
crisitem.author.orcid | 0000-0001-9399-3889 | - |
crisitem.author.orcid | 0000-0003-2953-210X | - |
crisitem.author.orcid | 0000-0003-4979-3761 | - |
crisitem.author.orcid | 0000-0001-7791-6154 | - |
crisitem.author.orcid | 0000-0002-2442-7952 | - |
crisitem.author.parentorg | National Taiwan University Hospital | - |
crisitem.author.parentorg | College of Medicine | - |
crisitem.author.parentorg | National Taiwan University Hospital Yun-Lin Branch | - |
crisitem.author.parentorg | College of Medicine | - |
crisitem.author.parentorg | National Taiwan University Hospital | - |
crisitem.author.parentorg | College of Medicine | - |
crisitem.author.parentorg | National Taiwan University Hospital | - |
crisitem.author.parentorg | National Taiwan University Hospital | - |
crisitem.author.parentorg | National Taiwan University Hospital | - |
crisitem.author.parentorg | College of Medicine | - |
crisitem.author.parentorg | National Taiwan University Hospital | - |
顯示於: | 臨床醫學研究所 |
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