Efficacy of telaprevir and boceprevir in treatment-naive and treatment-experienced genotype 1 chronic hepatitis C patients: an indirect comparison using Bayesian network meta-analysis

被引:10
作者
Cure, S. [1 ]
Diels, J. [2 ]
Gavart, S. [3 ]
Bianic, F. [1 ]
Jones, E. [1 ]
机构
[1] OptumInsight, Uxbridge UB8 1QG, Middx, England
[2] Janssen Pharmaceut NV, Janssen EMEA Hlth Econ & Market Access, Beerse, Belgium
[3] Janssen Pharmaceut NV, Worldwide Market Access, Janssen Global Serv, Beerse, Belgium
关键词
Bayesian; Boceprevir; Chronic hepatitis C; Indirect comparison; Network meta-analysis; Telaprevir; ISPOR TASK-FORCE; PLUS RIBAVIRIN; PEGINTERFERON ALPHA-2B;
D O I
10.1185/03007995.2012.734798
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background and aims: To indirectly compare the efficacy of telaprevir (TVR) and boceprevir (BOC) combined with peginterferon/ribavirin alpha-2a/2b (PR) in achieving sustained viral response (SVR) in treatment-naive 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-naive 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-naive and treatment-experienced patients.
引用
收藏
页码:1841 / 1856
页数:16
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