Borba Helena H, Wiens Astrid, Steimbach Laiza M, Perlin Cassio M, Tonin Fernanda S, Pedroso Maria L A, Fernandez-Llimos Fernando, Pontarolo Roberto
Department of Pharmacy, Pharmaceutical Sciences Postgraduate Research Program, Federal University of Paraná, Campus III, Av. Pref. Lothário Meissner, 632, Jardim Botânico, Curitiba, PR, 80210-170, Brazil.
Gastroenterology Service, Hospital de Clínicas, Federal University of Paraná, Curitiba, Brazil.
Eur J Clin Pharmacol. 2017 Jan;73(1):1-14. doi: 10.1007/s00228-016-2146-6. Epub 2016 Oct 19.
This study aimed to compare the efficacy among direct-acting antiviral agents (first and second-generation direct-acting antiviral agents (DAAs)) with placebo and with standard dual therapy (pegylated interferon + ribavirin (Peg-IFN + RBV)) in terms of rapid virologic response (RVR) and sustained virologic response (SVR) in chronic hepatitis C genotype 1 treatment.
We performed a systematic review of randomized controlled trials (RCTs) in MEDLINE, International Pharmaceutical Abstracts, Cochrane Library, SCIELO, and Scopus and conducted a network meta-analysis to compare the efficacy of boceprevir (BOC), daclatasvir (DCV), grazoprevir, simeprevir (SMV) and telaprevir (TVR), in treatment-naive and treatment-experienced patients.
Sixteen studies encompassing 7171 patients were analysed. Associations between DAAs therapies (IFN-free regimens) could not be addressed since no common comparator was found in the RCTs among these associations and the other agents included in the present analysis. All agents were more efficacious than placebo or Peg-IFN + RBV in terms of RVR, while only BOC and SMV showed statistically significant superiority for the SVR outcome when compared to placebo or standard dual therapy. No significant differences between the DAAs were observed. The analysis prioritized treatment with DCV for both efficacy outcomes. Node-splitting analysis showed that our networks are robust (p > 0.05).
The superiority of DAAs over placebo or standard dual therapy with Peg-IFN + RBV was confirmed, indicating the greater efficacy of DCV. This study is the first network meta-analysis that included RVR as an outcome in the evaluation of these agents via indirect comparison. Further investigation should be carried out addressing safety and tolerability outcomes.
本研究旨在比较直接作用抗病毒药物(第一代和第二代直接作用抗病毒药物(DAA))与安慰剂以及标准双重疗法(聚乙二醇干扰素+利巴韦林(Peg-IFN + RBV))在慢性丙型肝炎基因1型治疗中快速病毒学应答(RVR)和持续病毒学应答(SVR)方面的疗效。
我们对MEDLINE、国际药学文摘、考克兰图书馆、科学电子图书馆在线(SCIELO)和Scopus中的随机对照试验(RCT)进行了系统评价,并进行了网状Meta分析,以比较博赛匹韦(BOC)、达卡他韦(DCV)、格卡瑞韦、西米普明(SMV)和特拉匹韦(TVR)在初治和经治患者中的疗效。
分析了16项研究,共7171例患者。由于在这些关联的RCT中未找到共同对照,且本分析中包含的其他药物也未找到共同对照,因此无法探讨DAA疗法(不含干扰素方案)之间的关联。就RVR而言,所有药物都比安慰剂或Peg-IFN + RBV更有效,而与安慰剂或标准双重疗法相比,只有BOC和SMV在SVR结果上显示出统计学上的显著优势。未观察到DAA之间的显著差异。对于这两个疗效结果,分析优先选择DCV治疗。节点拆分分析表明我们的网络是稳健的(p>0.05)。
证实了DAA优于安慰剂或Peg-IFN + RBV的标准双重疗法,表明DCV疗效更佳。本研究是第一项将RVR作为通过间接比较评估这些药物疗效的网状Meta分析。应进一步研究安全性和耐受性结果。