Cost-effectiveness analysis of roadmap models in chronic hepatitis B using tenofovir as the rescue therapy

Antivir Ther. 2010;15(2):145-55. doi: 10.3851/IMP1496.

Abstract

Background: The roadmap approach is recommended to guide chronic hepatitis B treatment. We evaluated the cost-effectiveness of various treatment strategies in the global market.

Methods: Lamivudine and telbivudine were tested in roadmap models with switch-to tenofovir if HBV was detectable at week 24 or add-on tenofovir if resistance developed at year 1. Tenofovir and entecavir were tested as continuous monotherapy. In the reference arm, lamivudine was used with add-on tenofovir if resistance developed at year 1. The primary measure of effectiveness was undetectable HBV DNA at year 2. Cost-effectiveness was measured by incremental cost-effectiveness ratio (ICER) in US dollars against the reference arm.

Results: In the US and Germany, costs of the reference arms were US $14,486 and US $9,998 for hepatitis B e antigen (HBeAg)-positive and US $11,398 and US $7,531 for HBeAg-negative patients, respectively. In HBeAg-positive patients, the lamivudine roadmap was most cost-effective (ICER US $15,260 in the US and US $29,113 in Germany) with comparable effectiveness (75.1%) to other strategies. In HBeAg-negative patients, tenofovir and entecavir monotherapies were most effective (91-96%) and cost-effective (ICER US $31,297-43,387 in the US and US $53,976-59,822 in Germany). In Asia, where telbivudine cost was lower, both telbivudine and lamivudine roadmaps were cost-effective in HBeAg-positive patients. Tenofovir would be most cost-effective in HBeAg-negative patients if its cost equaled that of telbivudine in Asia.

Conclusions: In HBeAg-positive patients, lamivudine roadmap was most cost-effective; in Asia, telbivudine roadmap had comparable cost-effectiveness to lamivudine roadmap because of the relatively low price of telbivudine. In HBeAg-negative patients, entecavir and tenofovir monotherapies were more cost-effective than the roadmap models.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adenine / administration & dosage
  • Adenine / analogs & derivatives
  • Adenine / economics
  • Antiviral Agents* / administration & dosage
  • Antiviral Agents* / economics
  • Asia
  • Cost-Benefit Analysis
  • DNA, Viral / blood
  • Decision Support Techniques*
  • Drug Administration Schedule
  • Drug Resistance, Viral
  • Drug Therapy, Combination
  • Germany
  • Hepatitis B virus / drug effects
  • Hepatitis B, Chronic* / drug therapy
  • Hepatitis B, Chronic* / economics
  • Hepatitis B, Chronic* / virology
  • Humans
  • Lamivudine / administration & dosage
  • Lamivudine / economics
  • Models, Economic
  • Nucleosides* / administration & dosage
  • Nucleosides* / economics
  • Organophosphonates / administration & dosage
  • Organophosphonates / economics
  • Pyrimidinones* / administration & dosage
  • Pyrimidinones* / economics
  • Salvage Therapy* / economics
  • Telbivudine
  • Tenofovir
  • Thymidine / analogs & derivatives
  • Treatment Outcome
  • United States

Substances

  • Antiviral Agents
  • DNA, Viral
  • Nucleosides
  • Organophosphonates
  • Pyrimidinones
  • Telbivudine
  • Lamivudine
  • Tenofovir
  • Adenine
  • Thymidine