@article{abf4774103e04fefb856b241b0ced96e,
title = "Ledipasvir/sofosbuvir for HCV genotype 1, 2, 4–6 infection: Real-world evidence from a nationwide registry in Taiwan",
abstract = "Background/purpose: The Taiwan Association for the Study of the Liver (TASL) HCV Registry (TACR) is a nationwide registry of chronic hepatitis C patients in Taiwan. This study evaluated antiviral effectiveness of ledipasvir (LDV)/sofosbuvir (SOF) in patients in the TACR. Methods: Patients enrolled in TACR from 2017–2020 treated with LDV/SOF were eligible. The primary outcome was the proportion of patients with sustained virologic response 12 weeks after end of treatment (SVR12). Results: 5644 LDV/SOF ± ribavirin-treated patients were included (mean age: 61.4 years; 54.4% female). Dominant viral genotypes were GT1 (50.8%) and GT2 (39.3%). 1529 (27.1%) patients had liver cirrhosis, including 201 (3.6%) with liver decompensation; 686 (12.2%) had chronic kidney disease. SVR12 was achieved in 98.6% of the overall population and in 98.2% and 98.7% of patients with and without cirrhosis, respectively. SVR12 rates in patients with compensated cirrhosis treated with LDV/SOF without RBV were >98%, regardless of prior treatment experience. SVR12 was 98.6%, 98.4%, 100%, 100%, and 98.7% among those with GT1, GT2, GT4, GT5, and GT6 infections, respectively. Although patient numbers were relatively small, SVR12 rates of 100% were reported in patients infected with HCV GT2, GT5, and GT6 with decompensated cirrhosis and 98% in patients with severely compromised renal function. LDV/SOF adherence ≤60% (P < 0.001) was the most important factor associated with treatment failure. Incidence of adverse events was 15.8%, with fatigue being the most common. Conclusion: LDV/SOF is effective and well tolerated in routine clinical practice in Taiwan. Cure rates were high across patient populations.",
keywords = "Direct-acting antiviral, Hepatitis C virus, Ledipasvir, Real-world, Sofosbuvir",
author = "{TACR investigators} and Lo, {Ching Chu} and Huang, {Chung Feng} and Cheng, {Pin Nan} and Tseng, {Kuo Chih} and Chen, {Chi Yi} and Kuo, {Hsing Tao} and Huang, {Yi Hsiang} and Tai, {Chi Ming} and Peng, {Cheng Yuan} and Bair, {Ming Jong} and Chen, {Chien Hung} and Yeh, {Ming Lun} and Lin, {Chih Lang} and Lin, {Chun Yen} and Lee, {Pei Lun} and Chong, {Lee Won} and Hung, {Chao Hung} and Chang, {Te Sheng} and Huang, {Jee Fu} and Yang, {Chi Chieh} and Hu, {Jui Ting} and Lin, {Chih Wen} and Chen, {Chun Ting} and Wang, {Chia Chi} and Su, {Wei Wen} and Hsieh, {Tsai Yuan} and Lin, {Chih Lin} and Tsai, {Wei Lun} and Lee, {Tzong Hsi} and Chen, {Guei Ying} and Wang, {Szu Jen} and Chang, {Chun Chao} and Mo, {Lein Ray} and Yang, {Sheng Shun} and Wu, {Wen Chih} and Huang, {Chia Sheng} and Hsiung, {Chou Kwok} and Kao, {Chien Neng} and Tsai, {Pei Chien} and Liu, {Chen Hua} and Lee, {Mei Hsuan} and Liu, {Chun Jen} and Dai, {Chia Yen} and Chuang, {Wan Long} and Lin, {Han Chieh} and Kao, {Jia Horng} and Yu, {Ming Lung}",
note = "Funding Information: The authors would like to thank the Taiwan Association for the Study of Liver (TASL) , the TASL Foundation , and the Taiwan Liver Research Foundation for grant support and the TACR study group for data collection. We also thank the Center for Medical Informatics and Statistics of Kaohsiung Medical University for providing administrative and funding support. We acknowledge medical writing assistance from Julia Heagerty, PhD, associated with Obsidian Healthcare Group, Westerham, UK, funded by Gilead Sciences Hong Kong Ltd . Gilead Sciences had no control over the final content of this manuscript. Funding Information: The study was supported by grants from Kaohsiung Medical University ( MOST 109-2314-B-037-044 ; Center for Liquid Biopsy , KMU-TC108B06 ; Cohort Research Center , KMU-TC108B07 , KMU-DK109002 ; Center for Cancer Research KMU Global Networking Talent Plan Grant 105KMUOR08 ; Center for Liquid Biopsy and Cohort Research , KMU-TC109B05 ) and Kaohsiung Medical University Hospital ( KMUH-DK109005∼1 , KMUH-DK109002 , KMUH108-8R05 , KMUH108-8R09 , MOHW109-TDU-B-212-114006 ). Funding Information: M-L.Y. reports research support from AbbVie, Abbott, BMS, Gilead Sciences, Merck, and Roche; consultancy for AbbVie, Abbott, Ascletis, BMS, Gilead Sciences, J&J, Merck, Novartis, Pharmaessential, and Roche; speaker fees for AbbVie, Abbott, Ascletis, BMS, Gilead Sciences, Merck, Pharmaessential, and Roche. C–F.H. reports speaker fees for AbbVie, BMS, Gilead Sciences, Merck, and Roche. C–H.L. reports participation in advisory boards for AbbVie, Gilead Sciences, and Merck Sharp & Dohme; speaker fees for Abbott, AbbVie, Gilead Sciences, and Merck Sharp & Dohme; research grants from AbbVie, Gilead Sciences, and Merck Sharp & Dohme. All other authors have no conflicts of interest to declare. P–N C reports participation in advisory board for AbbVie, Gilead Sciences, and Merck Sharp & Dohme. Speaker for Abbott, AbbVie, Gilead Sciences, and Merck Sharp & Dohme. Research grants from Gilead Sciences and Merck Sharp & Dohme. J-H K reports participation in speaker, consultant and/or advisory board member for AbbVie, Arbutus Biopharma, Bristol Myers Squibb, Fujirebio, Gilead Sciences, Johnson & Johnson, MSD, Polaris, Sysmex and Roche. Publisher Copyright: {\textcopyright} 2022 Formosan Medical Association",
year = "2022",
doi = "10.1016/j.jfma.2022.01.012",
language = "English",
volume = "121",
pages = "1567--1578",
journal = "Journal of the Formosan Medical Association",
issn = "0929-6646",
publisher = "Elsevier Science Publishers B.V.",
number = "8",
}