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  4. Glecaprevir/pibrentasvir for patients with chronic hepatitis C virus infection: Real-world effectiveness and safety in Taiwan
 
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Glecaprevir/pibrentasvir for patients with chronic hepatitis C virus infection: Real-world effectiveness and safety in Taiwan

Journal
Liver International
Journal Volume
40
Journal Issue
4
Pages
758-768
Date Issued
2020
Author(s)
CHEN-HUA LIU  
CHUN-JEN LIU  
CHIEN-CHING HUNG  
SZU-MIN HSIEH  
TUNG-HUNG SU  
HSIN-YUN SUN  
TAI-CHUNG TSENG  
PEI-JER CHEN  
DING-SHINN CHEN  
JIA-HORNG KAO  
DOI
10.1111/liv.14295
URI
https://www.scopus.com/inward/record.uri?eid=2-s2.0-85075444848&doi=10.1111%2fliv.14295&partnerID=40&md5=1992f80b8028d8d13b0a6600fe97e78d
https://scholars.lib.ntu.edu.tw/handle/123456789/535382
Abstract
Background & Aims: Large-scale data regarding the real-world effectiveness and safety of glecaprevir/pibrentasvir (GLE/PIB) for patients with chronic hepatitis C virus (HCV) infection were limited in East Asia. We aimed to evaluate the clinical performance of GLE/PIB in different HCV populations in Taiwan. Methods: A total of 658 chronic HCV patients with compensated liver diseases receiving GLE/PIB for 8 (n?=?549), 12 (n?=?103) or 16 (n?=?6) weeks were retrospectively enrolled. The effectiveness was determined by sustained virologic response at off-therapy 12?weeks (SVR12). Patient characteristics potentially related to SVR12 and the safety profiles were also assessed. Results: By evaluable population (EP) and per-protocol (PP) analyses, the overall SVR12 rate was 98.2% (95% confidence interval (CI): 96.8%-99.0%) and 99.4% (95% CI: 98.4%-99.8%). The SVR12 rates were 98.9% (95% CI: 97.6%-99.5%), 94.2% (95% CI: 87.9%-97.3%) and 100% (95% CI: 60.1%-100%) in patients receiving 8, 12 and 16?weeks of treatment respectively. A total of 656 (99.7%) patients completed the scheduled treatment. The SVR12 rates were comparable regardless of baseline characteristics or week 4 viral decline. Twenty (3.0%) patients had serious adverse events (AEs), but none were not related to GLE/PIB. The two most common AEs were pruritus (7.8%) and fatigue (5.5%). Two (0.3%) and no patients had ?3-fold upper limit of normal (ULN) for total bilirubin and alanine aminotransferase (ALT) levels. Conclusions: GLE/PIB for 8-16?weeks is effective and well-tolerated for patients with chronic HCV infection in Taiwan. ? 2019 John Wiley & Sons A/S. Published by John Wiley & Sons Ltd
SDGs

[SDGs]SDG3

Other Subjects
alanine aminotransferase; bilirubin; glecaprevir plus pibrentasvir; adult; alanine aminotransferase blood level; Article; bilirubin blood level; chronic hepatitis C; clinical effectiveness; drug safety; fatigue; female; human; major clinical study; male; middle aged; patient compliance; pruritus; retrospective study; sustained virologic response; Taiwan
Publisher
Blackwell Publishing Ltd
Type
journal article

臺大位居世界頂尖大學之列,為永久珍藏及向國際展現本校豐碩的研究成果及學術能量,圖書館整合機構典藏(NTUR)與學術庫(AH)不同功能平台,成為臺大學術典藏NTU scholars。期能整合研究能量、促進交流合作、保存學術產出、推廣研究成果。

To permanently archive and promote researcher profiles and scholarly works, Library integrates the services of “NTU Repository” with “Academic Hub” to form NTU Scholars.

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