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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BMC
2021-07-01
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Series: | Virology Journal |
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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. |
first_indexed | 2024-12-22T08:35:06Z |
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id | doaj.art-1d837f09573540f19ac3428a40b0427c |
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issn | 1743-422X |
language | English |
last_indexed | 2024-12-22T08:35:06Z |
publishDate | 2021-07-01 |
publisher | BMC |
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series | Virology Journal |
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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