...
首页> 外文期刊>Current medical research and opinion >Efficacy of telaprevir and boceprevir in treatment-na?ve and treatment-experienced genotype 1 chronic hepatitis C patients: An indirect comparison using Bayesian network meta-analysis
【24h】

Efficacy of telaprevir and boceprevir in treatment-na?ve and treatment-experienced genotype 1 chronic hepatitis C patients: An indirect comparison using Bayesian network meta-analysis

机译:Telaprevir和Boceprevir在治疗中的疗效和治疗经验丰富的基因型1慢性丙型肝炎患者:使用贝叶斯网络荟萃分析的间接比较

获取原文
获取原文并翻译 | 示例
   

获取外文期刊封面封底 >>

       

摘要

Background and aims: To indirectly compare the efficacy of telaprevir (TVR) and boceprevir (BOC) combined with peginterferon/ribavirin ?2a/2b (PR) in achieving sustained viral response (SVR) in treatment-na飗e and treatment-experienced patients with genotype 1 chronic hepatitis C virus (HCV) infection. Methods: A systematic literature review was conducted to identify randomized controlled trials reporting the efficacy of PR-based treatment in genotype 1 chronic HCV patients. A Bayesian network meta-analysis was performed on the endpoint of SVR, assuming fixed study effects. For treatment-experienced patients, only previous relapsers and partial responders were included, as no results in prior null responders were available for boceprevir. Results: Eleven publications were included. In treatment-na飗e patients, the odds ratios (OR) (posterior median [95% credible interval]) for telaprevir (12 weeks response guided treatment [RGT] 24/48 weeks PR) and boceprevir (24 weeks RGT 28/48 weeks PR) versus PR were respectively 3.80 (2.78-5.22) and 2.99 (2.23-4.01). The OR for telaprevir versus boceprevir was 1.42 (0.89-2.25), with a probability for telaprevir being more effective (P[OR>1]) of 0.93. In treatment-experienced patients, the OR of telaprevir (12 weeks 48 weeks PR) and boceprevir (32 weeks RGT 36/48 weeks PR) versus PR were respectively 13.11 (7.30-24.43) and 5.36 (2.90-10.30). The OR for telaprevir versus boceprevir was 2.45 (1.02-5.80), with telaprevir having a probability of 0.98 of being more effective. Limitations: The main limitation of this study is the low number of trials included in the analysis, especially for the treatment-experienced patient population, which only allowed random-effect models to be explored. We tried to identify potential biases due to study heterogeneity. Conclusions: In the absence of direct comparative head-to-head studies between telaprevir and boceprevir for the treatment of chronic HCV genotype 1 patients, an indirect comparison based on Bayesian network meta-analysis suggests better efficacy for telaprevir than boceprevir in both treatment-na飗e and treatment- experienced patients.
机译:背景和目标:间接地比较Telaprevir(TVR)和Boceprevir(Boc)的疗效与Peginterferon /利巴韦林(PR)在治疗持续的病毒反应(SVR)中的治疗中的持续病毒反应(SVR)和治疗经验丰富的患者中的疗效进行比较用基因型1慢性丙型肝炎病毒(HCV)感染。方法:进行系统文献综述,以确定随机对照试验报告PR型治疗在基因型1慢性HCV患者中的疗效。假设固定的研究效果,对SVR的终点进行了贝叶斯网络元分析。对于经验丰富的患者,只有先前的复发者和部分响应者,因为BocePrevir可以获得先前空响应者的结果。结果:包括11个出版物。在治疗中,患者,Telaprevir(12周回复引导治疗PR)和BocePrevir(24周RGT 28/48周PR)与PR分别为3.80(2.78-5.22)和2.99(2.23-4.01)。 Teladrevir与Boceprevir为1.42(0.89-2.25),Teladrevir更有效的概率(p [或> 1])0.93。在治疗经验丰富的患者中,Telaprevir(12周48周PR)和Boceprevir(32周RGT 36/48周PR)与PR分别为PR分别为13.11(7.30-24.43)和5.36(2.90-10.30)。 Telaprevir与Boceprevir为2.45(1.02-5.80),Telaprevir具有0.98更有效的概率。局限性:本研究的主要限制是分析中包含的较少的试验,特别是对于治疗经验丰富的患者人群,这只允许探索随机效果模型。我们试图识别由于研究异质性导致的潜在偏见。结论:在Telaprevir与Boceprevir之间的直接比较头脑研究的情况下,慢性HCV基因型1例患者的间接比较,基于贝叶斯网络荟萃分析的间接比较表明对Teladrevir的疗效比ProcePrevir在治疗中飗e和治疗 - 经验丰富的患者。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号