Cost-effectiveness of truncated therapy for hepatitis C based on rapid virologic response

Value Health. 2012 Sep-Oct;15(6):876-86. doi: 10.1016/j.jval.2012.06.010. Epub 2012 Aug 9.

Abstract

Background: Shortened courses of treatment with pegylated interferon alfa and ribavirin for patients with hepatitis C virus infection who experience rapid virologic response can be effective in appropriately selected patients. The cost-effectiveness of truncated therapy is not known.

Objective: To assess the cost-effectiveness of response-guided therapy versus standard-duration therapy on the basis of best available evidence.

Methods: We developed a decision model for chronic hepatitis C virus infection representing two treatment strategies: 1) standard-duration therapy with pegylated interferon alfa and ribavirin for 48 weeks in patients with genotype 1 or 4 and for 24 weeks in patients with genotype 2 or 3 and 2) truncated therapy (i.e., 50% decrease in treatment duration) in patients with rapid virologic response. Patients for whom truncated therapy failed began standard-duration therapy guided by genotype. We used a Markov model to estimate lifetime costs and quality-adjusted life-years.

Results: In the base-case analysis, mean lifetime costs were $46,623 ± $2,483 with standard-duration therapy and $42,354 ± $2,489 with truncated therapy. Mean lifetime quality-adjusted life-years were similar between the groups (17.1 ± 0.7 with standard therapy; 17.2 ± 0.7 with truncated therapy). Across model simulations, the probability of truncated therapy being economically dominant (i.e., both cost saving and more effective) was 78.6%. The results were consistent when we stratified the data by genotype. In one-way sensitivity analyses, the results were sensitive only to changes in treatment efficacy.

Conclusion: Truncated therapy based on rapid virologic response is likely to be cost saving for treatment-naive patients with chronic hepatitis C virus infection. Cost-effectiveness varied with small changes in relative treatment efficacy.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adult
  • Antiviral Agents / administration & dosage*
  • Antiviral Agents / economics*
  • Comparative Effectiveness Research
  • Cost-Benefit Analysis
  • Drug Therapy, Combination
  • Female
  • Hepacivirus / drug effects*
  • Hepacivirus / genetics*
  • Hepatitis C, Chronic / drug therapy*
  • Hepatitis C, Chronic / virology*
  • Humans
  • Interferon-alpha / administration & dosage*
  • Interferon-alpha / economics*
  • Interferon-alpha / genetics
  • Interferon-alpha / therapeutic use
  • Male
  • Middle Aged
  • Models, Theoretical
  • Polyethylene Glycols / economics
  • Polyethylene Glycols / therapeutic use
  • Recombinant Proteins / economics
  • Recombinant Proteins / therapeutic use
  • Ribavirin / administration & dosage*
  • Ribavirin / economics*
  • Treatment Outcome
  • Young Adult

Substances

  • Antiviral Agents
  • Interferon-alpha
  • Recombinant Proteins
  • Polyethylene Glycols
  • Ribavirin
  • peginterferon alfa-2a