A meta-analysis platform methodology for determining the comparative effectiveness of antihepatitis C virus regimens

J Comp Eff Res. 2015 Mar;4(2):101-14. doi: 10.2217/cer.14.69.

Abstract

Aim: Many hepatitis C virus regimens are unlikely to be compared head to head. In more difficult to treat populations where there is no standard of care, trials are single arm. We describe a flexible meta-analysis platform in this setting.

Methods: Our meta-analysis is literature based. We illustrate our methodology and show how inference can be extended to single-arm trials.

Results: As an example, in the single arm setting, a regimen with response rates of 84, 72 and 54% in genotype 1a across treatment naive, previous partial responders and previous null responders, respectively, would have 95% probability of superiority to IFN-α + RBV + TPV.

Conclusion: This is a rigorous approach to comparative effectiveness that accounts for varying patient populations and plans for the incorporation of emerging treatments.

Keywords: Bayesian hierarchical model; boceprevir; comparative effectiveness; hepatitis C; meta-analysis; sustained virologic response; telaprevir.

Publication types

  • Meta-Analysis
  • Research Support, Non-U.S. Gov't
  • Review

MeSH terms

  • Algorithms
  • Antiviral Agents / therapeutic use*
  • Bayes Theorem
  • Comparative Effectiveness Research
  • Drug Therapy, Combination
  • Hepacivirus
  • Hepatitis C / drug therapy*
  • Humans
  • Interferon-alpha / therapeutic use*
  • Oligopeptides / therapeutic use*
  • Proline / analogs & derivatives*
  • Proline / therapeutic use
  • Ribavirin / therapeutic use*
  • Treatment Outcome

Substances

  • Antiviral Agents
  • Interferon-alpha
  • Oligopeptides
  • Ribavirin
  • telaprevir
  • N-(3-amino-1-(cyclobutylmethyl)-2,3-dioxopropyl)-3-(2-((((1,1-dimethylethyl)amino)carbonyl)amino)-3,3-dimethyl-1-oxobutyl)-6,6-dimethyl-3-azabicyclo(3.1.0)hexan-2-carboxamide
  • Proline