Publication: Real-world effectiveness and safety of sofosbuvir and nonstructural protein 5A inhibitors for chronic hepatitis C genotype 1, 2, 3, 4, or 6: A multicentre cohort study
Issued Date
2020-03-05
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ISSN
1471230X
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2-s2.0-85081200562
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Mahidol University
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SCOPUS
Bibliographic Citation
BMC Gastroenterology. Vol.20, No.1 (2020)
Suggested Citation
Phunchai Charatcharoenwitthaya, Virasak Wongpaitoon, Piyawat Komolmit, Wattana Sukeepaisarnjaroen, Pisit Tangkijvanich, Teerha Piratvisuth, Theeranun Sanpajit, Chinnavat Sutthivana, Chalermrat Bunchorntavakul, Abhasnee Sobhonslidsuk, Soonthorn Chonprasertsuk, Chotipong Siripipattanamongkol, Supatsri Sethasine, Tawesak Tanwandee Real-world effectiveness and safety of sofosbuvir and nonstructural protein 5A inhibitors for chronic hepatitis C genotype 1, 2, 3, 4, or 6: A multicentre cohort study. BMC Gastroenterology. Vol.20, No.1 (2020). doi:10.1186/s12876-020-01196-0 Retrieved from: https://repository.li.mahidol.ac.th/handle/20.500.14594/53727
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Title
Real-world effectiveness and safety of sofosbuvir and nonstructural protein 5A inhibitors for chronic hepatitis C genotype 1, 2, 3, 4, or 6: A multicentre cohort study
Author(s)
Phunchai Charatcharoenwitthaya
Virasak Wongpaitoon
Piyawat Komolmit
Wattana Sukeepaisarnjaroen
Pisit Tangkijvanich
Teerha Piratvisuth
Theeranun Sanpajit
Chinnavat Sutthivana
Chalermrat Bunchorntavakul
Abhasnee Sobhonslidsuk
Soonthorn Chonprasertsuk
Chotipong Siripipattanamongkol
Supatsri Sethasine
Tawesak Tanwandee
Virasak Wongpaitoon
Piyawat Komolmit
Wattana Sukeepaisarnjaroen
Pisit Tangkijvanich
Teerha Piratvisuth
Theeranun Sanpajit
Chinnavat Sutthivana
Chalermrat Bunchorntavakul
Abhasnee Sobhonslidsuk
Soonthorn Chonprasertsuk
Chotipong Siripipattanamongkol
Supatsri Sethasine
Tawesak Tanwandee
Other Contributor(s)
Chulalongkorn University
Bhumibol Adulyadej Hospital
Bumrungrad International Hospital
Vajira Hospital
Khon Kaen University
Faculty of Medicine, Ramathibodi Hospital, Mahidol University
Thammasat University
Faculty of Medicine, Siriraj Hospital, Mahidol University
Phramongkutklao College of Medicine
Prince of Songkla University
Rajavithi Hospital
Chiangrai Prachanukroh Hospital
Bhumibol Adulyadej Hospital
Bumrungrad International Hospital
Vajira Hospital
Khon Kaen University
Faculty of Medicine, Ramathibodi Hospital, Mahidol University
Thammasat University
Faculty of Medicine, Siriraj Hospital, Mahidol University
Phramongkutklao College of Medicine
Prince of Songkla University
Rajavithi Hospital
Chiangrai Prachanukroh Hospital
Abstract
© 2020 The Author(s). Background: We investigated real-world effectiveness and safety of sofosbuvir and the nonstructural protein 5A inhibitors in the treatment of patients infected with hepatitis C virus (HCV) genotypes 1, 2, 3, 4, or 6. Methods: We analyzed data from 1021 patients with HCV infection (506 with genotype 1; 16 with genotype 2; 314 with genotype 3; 13 with genotype 4; 166 with genotype 6) who received 12 to 24 weeks of daclatasvir plus sofosbuvir (n = 767), ledipasvir/sofosbuvir (n = 197), or sofosbuvir/velpatasvir (n = 57), with or without ribavirin in 12 centers across Thailand to estimate sustained virologic response at post-treatment week 12 (SVR12). Results: Overall, SVR12 rate was 98.0% (95% confidence interval [CI], 96.7-98.8%) with daclatasvir plus sofosbuvir, 97.9% (95% CI, 94.8-99.2%) with ledipasvir/sofosbuvir, and 96.5% (95% CI, 88.1-99.0%) with sofosbuvir/velpatasvir. SVR12 was achieved by 99.2% (95% CI, 97.9-99.7%) of subjects with genotype 1 infection, 100% (95% CI, 78.5-100%) of those with genotype 2 infection, 96.7% (95% CI, 94.0-98.2%) of those with genotype 3 infection, 90.9% (95% CI, 62.3-98.4%) of those with genotype 4 infection, and 96.7% (95% CI 92.5-98.6%) of those with genotype 6 infection. Patients with advanced liver disease were at risk of treatment failure. Only four patients discontinued treatment before week 4 due to non-hepatic adverse events. Conclusions: In this large cohort of patients with various HCV genotypes managed in the real-world practice setting, daclatasvir plus sofosbuvir, ledipasvir/sofosbuvir, and sofosbuvir/velpatasvir achieved high SVR rates with good safety profile, comparable to those observed in clinical trials.