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Review
. 2016 Sep 15;5(1):1569.
doi: 10.1186/s40064-016-3218-x. eCollection 2016.

Daclatasvir combined with peginterferon-α and ribavirin for the treatment of chronic hepatitis C: a meta-analysis

Affiliations
Review

Daclatasvir combined with peginterferon-α and ribavirin for the treatment of chronic hepatitis C: a meta-analysis

Qin Peng et al. Springerplus. .

Abstract

Daclatasvir, a HCV NS5A inhibitor, is a new direct-acting antiviral drug for chronic hepatitis C (CHC). This study aimed to evaluate the efficacy and safety of daclatasvir combined with peginterferon-α (pegIFN-α) and ribavirin (RBV) for the treatment of CHC. The databases of PUBMED, EMBASE, COCHRANE, WANFANG, and CNKI were retrieved to identify eligible studies. Pooled risk ratio (RR) and 95 % confidence interval (CI) were calculated using random or fixed models. A total of six RCTs including 1100 adult patients with CHC met the inclusion criteria and the patients were infected with HCV genotype 1-4, with the genotype 1 infection accounting for 73.1 %. Meta-analysis showed daclatasvir-based combination therapy yielded a significantly higher probability of achieving the overall RVR (46.43 vs. 18.97 %) with pooled RR of 3.77 (95 % CI 1.95-7.28, p < 0.0001) and a slightly higher probability of achieving the overall SVR24 (65.08 vs. 47.77 %) with pooled RR of 1.41 (95 % CI 1.18-1.68, p < 0.0001), and did not show increased adverse events compared with the pegIFN-α/RBV regimen (control group). Subgroup analysis showed the rate of RVR and SVR24 in high-dose daclatasvir (60 mg/day) group were slightly higher than the overall results; the rate of RVR in low-dose daclatasvir (10 mg/day) group was also higher than the control group, but its SVR24 rate was similar between the two groups. Daclatasvir combined with pegIFN-α/RBV is effective and safe in treating adult patients with CHC, especially HCV genotype 1 infection, and daclatasvir (60 mg/day) is a better choice as compared with daclatasvir (10 mg/day).

Keywords: Chronic; Daclatasvir; Hepatitis C; Meta-analysis; Randomized controlled trials.

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Figures

Fig. 1
Fig. 1
Search strategy and flow of information relative to the meta-analysis
Fig. 2
Fig. 2
Forest plot of RVR rate of DCV + P/R and PBO + P/R for CHC
Fig. 3
Fig. 3
Forest plot of SVR rate of DCV + P/R and PBO + P/R for CHC
Fig. 4
Fig. 4
Forest plot of relapse rate of DCV + P/R and PBO + P/R for CHC
Fig. 5
Fig. 5
Forest plot of TDAE rate of DCV + P/R and PBO + P/R for CHC
Fig. 6
Fig. 6
Forest plot of RVR rate of DCV (60 mg/day) + P/R and PBO + P/R for CHC
Fig. 7
Fig. 7
Forest plot of SVR rate of DCV (60 mg/day) + P/R and PBO + P/R for CHC
Fig. 8
Fig. 8
Forest plot of RVR rate of DCV (10 mg/day) + P/R and PBO + P/R for CHC
Fig. 9
Fig. 9
Forest plot of SVR rate of DCV (10 mg/day) + P/R and PBO + P/R for CHC

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References

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