Efficacy and safety of ledipasvir/sofosbuvir for hepatitis C among drug users: a systematic review and meta-analysis

Abstract Background and aims Limited data is available on the efficacy of direct acting anti-viral drugs on hepatitis C in drug users. The aim of this meta-analysis was to comprehensively analyze the efficacy and safety of LDV/SOF in drug users infected with the hepatitis C virus (HCV). Methods The...

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Main Authors: Xue Yang, Yang Tang, Di Xu, Guang Zhang, Peng Xu, Houlin Tang, Lin Pang
Format: Article
Language:English
Published: BMC 2021-07-01
Series:Virology Journal
Subjects:
Online Access:https://doi.org/10.1186/s12985-021-01625-w
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author Xue Yang
Yang Tang
Di Xu
Guang Zhang
Peng Xu
Houlin Tang
Lin Pang
author_facet Xue Yang
Yang Tang
Di Xu
Guang Zhang
Peng Xu
Houlin Tang
Lin Pang
author_sort Xue Yang
collection DOAJ
description Abstract Background and aims Limited data is available on the efficacy of direct acting anti-viral drugs on hepatitis C in drug users. The aim of this meta-analysis was to comprehensively analyze the efficacy and safety of LDV/SOF in drug users infected with the hepatitis C virus (HCV). Methods The PubMed, Cochrane library, Embase and Web of Science databases were searched for articles published till April 2021 on HCV-positive drug users who were treated with ledipasvir/sofosbuvir (LDV/SOF). The primary endpoint was pooled sustained virological response at 12 weeks (SVR12) with 95% confidence interval (95% CI). Funnel plots and Egger’s test were used to assess the publication bias. Results A total of 12 studies and 711 subjects treated with LDV/SOF-based regimen for HCV were included, and the pooled SVR12 rate was 89.8% (95% CI 85.9–92.7). The pooled SVR12 rate of genotype 1 drug users was 92.4% (95% CI 88.6–95.0). Subgroup analysis showed that pooled SVR12 rates of patients treated with LDV/SOF and LDV/SOF ± RBV were 89.2% (95% CI 83.4–93.1), 90.4% (95% CI 83.6–94.5) respectively. In addition, the SVR12 rates were 88% (95% CI 70.7–95.7) for 8 weeks, 89.9% (95% CI 81.0–94.9) for 12 weeks and 82.2% (95% CI 24.9–98.5) for 24 weeks of treatment. Conclusion LDV/SOF is a safe and relatively effective treatment for hepatitis C in drug users.
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spelling doaj.art-1d837f09573540f19ac3428a40b0427c2022-12-21T18:32:22ZengBMCVirology Journal1743-422X2021-07-0118111310.1186/s12985-021-01625-wEfficacy and safety of ledipasvir/sofosbuvir for hepatitis C among drug users: a systematic review and meta-analysisXue Yang0Yang Tang1Di Xu2Guang Zhang3Peng Xu4Houlin Tang5Lin Pang6National Center for AIDS/STD Control and Prevention, Chinese Center for Disease Control and PreventionNational Center for AIDS/STD Control and Prevention, Chinese Center for Disease Control and PreventionNational Center for AIDS/STD Control and Prevention, Chinese Center for Disease Control and PreventionNational Center for AIDS/STD Control and Prevention, Chinese Center for Disease Control and PreventionNational Center for AIDS/STD Control and Prevention, Chinese Center for Disease Control and PreventionNational Center for AIDS/STD Control and Prevention, Chinese Center for Disease Control and PreventionNational Center for AIDS/STD Control and Prevention, Chinese Center for Disease Control and PreventionAbstract Background and aims Limited data is available on the efficacy of direct acting anti-viral drugs on hepatitis C in drug users. The aim of this meta-analysis was to comprehensively analyze the efficacy and safety of LDV/SOF in drug users infected with the hepatitis C virus (HCV). Methods The PubMed, Cochrane library, Embase and Web of Science databases were searched for articles published till April 2021 on HCV-positive drug users who were treated with ledipasvir/sofosbuvir (LDV/SOF). The primary endpoint was pooled sustained virological response at 12 weeks (SVR12) with 95% confidence interval (95% CI). Funnel plots and Egger’s test were used to assess the publication bias. Results A total of 12 studies and 711 subjects treated with LDV/SOF-based regimen for HCV were included, and the pooled SVR12 rate was 89.8% (95% CI 85.9–92.7). The pooled SVR12 rate of genotype 1 drug users was 92.4% (95% CI 88.6–95.0). Subgroup analysis showed that pooled SVR12 rates of patients treated with LDV/SOF and LDV/SOF ± RBV were 89.2% (95% CI 83.4–93.1), 90.4% (95% CI 83.6–94.5) respectively. In addition, the SVR12 rates were 88% (95% CI 70.7–95.7) for 8 weeks, 89.9% (95% CI 81.0–94.9) for 12 weeks and 82.2% (95% CI 24.9–98.5) for 24 weeks of treatment. Conclusion LDV/SOF is a safe and relatively effective treatment for hepatitis C in drug users.https://doi.org/10.1186/s12985-021-01625-wHepatitis CLedipasvir and sofosbuvirDrug usersSVR12Meta-analysis
spellingShingle Xue Yang
Yang Tang
Di Xu
Guang Zhang
Peng Xu
Houlin Tang
Lin Pang
Efficacy and safety of ledipasvir/sofosbuvir for hepatitis C among drug users: a systematic review and meta-analysis
Virology Journal
Hepatitis C
Ledipasvir and sofosbuvir
Drug users
SVR12
Meta-analysis
title Efficacy and safety of ledipasvir/sofosbuvir for hepatitis C among drug users: a systematic review and meta-analysis
title_full Efficacy and safety of ledipasvir/sofosbuvir for hepatitis C among drug users: a systematic review and meta-analysis
title_fullStr Efficacy and safety of ledipasvir/sofosbuvir for hepatitis C among drug users: a systematic review and meta-analysis
title_full_unstemmed Efficacy and safety of ledipasvir/sofosbuvir for hepatitis C among drug users: a systematic review and meta-analysis
title_short Efficacy and safety of ledipasvir/sofosbuvir for hepatitis C among drug users: a systematic review and meta-analysis
title_sort efficacy and safety of ledipasvir sofosbuvir for hepatitis c among drug users a systematic review and meta analysis
topic Hepatitis C
Ledipasvir and sofosbuvir
Drug users
SVR12
Meta-analysis
url https://doi.org/10.1186/s12985-021-01625-w
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