Economic evaluation of doravirine/tenofovir disoproxil fumarate/lamivudine for HIV-1-infected adults in Russia: a cost-minimization and budget impact analysis

Expert Rev Pharmacoecon Outcomes Res. 2022 Dec;22(8):1215-1220. doi: 10.1080/14737167.2022.2117162. Epub 2022 Oct 5.

Abstract

Background: In Russia, before 2022, the list of vital and essential drugs for HIV-infected patients previously untreated with antiretroviral drugs included the fixed-dose combination rilpivirine/tenofovir disoproxil fumarate/emtricitabine (RPV/TDF/FTC) but not doravirine/tenofovir disoproxil fumarate/lamivudine (DOR/TDF/3TC).

Methods: An indirect comparison of the efficacy of DOR/TDF/3TC and RPV/TDF/FTC defined by virologic suppression (HIV-1 RNA of <50 copies/mL at week 48) was made. The per-patient drug costs over 1 year were compared in a cost-minimization analysis. A budget impact analysis considered the costs to the healthcare system of including DOR/TDF/3TC as a treatment option for eligible patients in Russia over a 3-year time horizon.

Results: The indirect treatment comparison of DOR/TDF/3TC and RPV/TDF/FTC in treatment-naïve patients with baseline HIV-1 RNA 100,000 copies/ml or less showed no statistically significant difference (RR 0.914, 95% CI 0.833-1.003). In the cost-minimization analysis, the per-patient cost of one year of treatment with RPV/TDF/FTC and DOR/TDF/3TC was, respectively, ₽320,975 and ₽151,192, for a saving of ₽169,783. In the budget impact analysis, the adoption of DOR/TDF/3TC into clinical practice is expected to reduce drug costs by ₽333 million (23.8%) in year 3.

Conclusions: Fixed-dose combination DOR/TDF/3TC is equally effective and cost-saving compared to RPV/TDF/FTC from Russian vital and essential drugs list perspective.

Keywords: Antiretroviral therapy; HIV infection; doravirine; fixed-dose combination; human immunodeficiency virus; pharmacoeconomic analysis; rilpivirine.

MeSH terms

  • Adult
  • Anti-HIV Agents* / adverse effects
  • Cost-Benefit Analysis
  • Drug Combinations
  • Drugs, Essential*
  • Emtricitabine / pharmacology
  • Emtricitabine / therapeutic use
  • HIV Infections* / drug therapy
  • HIV Seropositivity* / drug therapy
  • HIV-1* / genetics
  • Humans
  • Lamivudine / adverse effects
  • RNA, Viral / pharmacology
  • RNA, Viral / therapeutic use
  • Tenofovir / pharmacology
  • Tenofovir / therapeutic use
  • Viral Load

Substances

  • Lamivudine
  • Tenofovir
  • Drugs, Essential
  • RNA, Viral
  • Emtricitabine
  • Anti-HIV Agents
  • Drug Combinations