Abstract | BACKGROUND AND AIM:
Sofosbuvir is a hepatitis C virus (HCV) NS5B polymerase inhibitor. The objective of this study was to explore the efficacy and safety of sofosbuvir for HCV genotype (GT) 2 and 3 infected patients. METHOD: We searched randomized controlled trials (RCTs) which analyzed the efficacy and safety of sofosbuvir-containing regimens for HCV GT 2/3 infected patients and collected data. The endpoints were sustained virological response 12- and 24-weeks after the cessation of therapy (SVR12 and SVR24), the adverse events (AEs) and the severe adverse events (SAEs). RESULTS: Eighteen trials comprising 2,975 HCV GT 2/3 infected patients were included. The pooled estimate SVR12, SVR24, AEs and SAEs rates were 84.6% (95% CI: 83.2-86.0), 83.7% (95% CI: 82.0-85.2), 83.8 (95% CI: 82.3-85.3) and 3.9 (95% CI: 3.2-4.8). The SVR12 rate of sofosbuvir-containing regimens for HCV GT 2 infection was higher than that for HCV GT 3 infection (95.7% vs. 80.8%). The sofosbuvir combined with velpatasvir (with or without ribavirin) regimen presented a higher SVR12 rate and lower AEs rate than the sofosbuvir combined with ribavirin (with or without peg-IFN) regimen (94.9% vs. 80.7% for SVR12 rate; 69.3% vs. 87.7% for AEs rate). CONCLUSIONS:
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Authors | Haozhi Fan, Peng Huang, Ting Tian, Jingjing Wu, Xueshan Xia, Yue Feng, Jie Wang, Rongbin Yu, Yun Zhang, Ming Yue |
Journal | Journal of gastrointestinal and liver diseases : JGLD
(J Gastrointestin Liver Dis)
Vol. 27
Issue 2
Pg. 159-168
(Jun 2018)
ISSN: 1842-1121 [Electronic] Romania |
PMID | 29922761
(Publication Type: Meta-Analysis)
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Chemical References |
- Antiviral Agents
- Sofosbuvir
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Topics |
- Antiviral Agents
(adverse effects, pharmacology, therapeutic use)
- Drug Therapy, Combination
- Genotype
- Hepacivirus
(drug effects, genetics)
- Hepatitis C, Chronic
(drug therapy, virology)
- Humans
- Randomized Controlled Trials as Topic
- Sofosbuvir
(adverse effects, pharmacology, therapeutic use)
- Sustained Virologic Response
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