From the Faculty of Medicine, University of British Columbia, Vancouver, British Columbia, Canada, Redwood Outcomes, Vancouver, British Columbia, Canada and Stanford Prevention Research Centre, Stanford University, Stanford, California, USA From the Faculty of Medicine, University of British Columbia, Vancouver, British Columbia, Canada, Redwood Outcomes, Vancouver, British Columbia, Canada and Stanford Prevention Research Centre, Stanford University, Stanford, California, USA
From the Faculty of Medicine, University of British Columbia, Vancouver, British Columbia, Canada, Redwood Outcomes, Vancouver, British Columbia, Canada and Stanford Prevention Research Centre, Stanford University, Stanford, California, USA.
QJM. 2015 Apr;108(4):299-306. doi: 10.1093/qjmed/hcu202. Epub 2014 Sep 19.
To conduct a network meta-analysis (NMA) to determine the comparative efficacy, as measured by sustained virological response (SVR), between boceprevir (BOC), telaprevir (TEL), faldaprevir (FAL), simeprevir (SIM) and sofosbuvir (SOF) in combination with peginterferon-ribavirin (PR) against a control of PR.
A literature search was conducted to identify randomized controlled trials (RCTs) including adult patients with hepatitis C virus genotype 1 who were naive to any prior therapy. RCTs assessing standard duration therapy (SDT) or response-guided therapy (RGT) BOC, TEL, FAL, SIM or SOF in combination with PR against a control of PR were eligible for inclusion. All RCTs must have provided SVR at either 12 or 24 weeks post-therapy cessation.
We included nine RCTs. All direct-acting antivirals (DAAs) were found to perform better than PR. Additionally, SDT FAL was found to be better than the 240 mg RGT FAL regimen with the PR lead-in. A sensitivity analysis excluding RCTs with only SVR at 12 weeks was consistent with the results of the primary analysis. A sensitivity analysis removing an RCT assessing SIM that reported SVR of >60% in the PR control group additionally found that RGT SIM was superior to the 240 mg RGT FAL regimen with the PR lead-in.
Our analyses indicate that SDT and RGT regimens of DAAs plus PR do not differ greatly in terms of SVR among treatment-naive hepatitis C genotype 1 patients. More advanced Bayesian network meta-analyses are likely needed to incorporate a comprehensive evidence base, expanding beyond randomized clinical trials.
通过网络荟萃分析(NMA)来确定博赛匹韦(BOC)、特拉匹韦(TEL)、法地昔洛韦(FAL)、西美瑞韦(SIM)和索磷布韦(SOF)联合聚乙二醇干扰素-利巴韦林(PR)与 PR 对照相比,在持续病毒学应答(SVR)方面的疗效比较。
进行文献检索,以确定包括初治丙型肝炎病毒基因型 1 成年患者的随机对照试验(RCT)。评估标准持续时间治疗(SDT)或应答指导治疗(RGT)BOC、TEL、FAL、SIM 或 SOF 联合 PR 与 PR 对照的 RCT 符合纳入标准。所有 RCT 必须在治疗停止后 12 或 24 周提供 SVR。
我们纳入了 9 项 RCT。所有直接作用抗病毒药物(DAA)均优于 PR。此外,与 PR 先导的 240mg RGT FAL 方案相比,SDT FAL 也表现更好。排除仅在 12 周时具有 SVR 的 RCT 的敏感性分析与主要分析结果一致。一项排除评估 SIM 的 RCT 的敏感性分析,该 RCT 报告 PR 对照组的 SVR >60%,另外发现 RGT SIM 优于 PR 先导的 240mg RGT FAL 方案。
我们的分析表明,在初治丙型肝炎基因型 1 患者中,DAA 联合 PR 的 SDT 和 RGT 方案在 SVR 方面没有太大差异。可能需要更先进的贝叶斯网络荟萃分析来纳入全面的证据基础,扩展到随机临床试验之外。