Fosamprenavir clinical study meta-analysis in ART-naïve subjects: rare occurrence of virologic failure and selection of protease-associated mutations

HIV Clin Trials. 2006 Nov-Dec;7(6):334-8. doi: 10.1310/hct0706-334.

Abstract

Background: In recent ritonavir-boosted protease inhibitor (PI) studies, high efficacy rates have been observed, with few PI mutations detected.

Method: To better understand the types of mutations observed and their phenotypic impact and the likelihood of virologic failure (VF) on a regimen that includes either a ritonavir-boosted or unboosted PI, fosamprenavir, a meta-analysis of three studies (NEAT, SOLO, and KLEAN) of 922 ART-naïve participants receiving boosted (FPV/r) or unboosted fosamprenavir (FPV) plus abacavir/lamivudine was performed. 70% of participants by the missing and discontinuation equals failure analysis and 95% by the observed analysis had HIV-RNA <400 copies/mL through 48 weeks. Paired genotypes (baseline and follow-up) were obtained for 74/85 participants meeting VF analysis criteria.

Results: FPV-associated resistance mutations were detected in 5/74 patients with VF, with 4/5 receiving unboosted FPV; in four patients viruses developed I54L or M and one developed the V32I+I47V combination. No virus from patients with VF receiving FPV/r had reduced FPV susceptibility (RS), whereas virus from 3/4 of participants with VF who received unboosted FPV and who acquired FPV mutations had FPV RS. Little PI cross-resistance was detected in the VF virus; RS was observed for lopinavir, saquinavir, nelfinavir, atazanavir, and indinavir in 0, 0, 2, 0, and 1 of 5 subjects, respectively.

Conclusion: These data suggest that inclusion of FPV as part of an initial HIV-treatment regimen is associated with low rates of VF. Selection of FPV resistance-associated mutations is unlikely, especially for FPV/r-containing regimens. If selection of FPV-associated mutations does occur, a second-line PI-containing regimen can be easily constructed.

Publication types

  • Meta-Analysis

MeSH terms

  • Anti-HIV Agents / pharmacology*
  • Antiretroviral Therapy, Highly Active
  • Carbamates / pharmacology*
  • Drug Interactions
  • Drug Resistance, Viral / genetics*
  • Furans
  • HIV Infections / drug therapy
  • HIV Protease / genetics*
  • HIV Protease / metabolism
  • HIV-1 / drug effects*
  • HIV-1 / genetics
  • Humans
  • Mutation / genetics
  • Organophosphates / pharmacology*
  • Selection, Genetic
  • Sulfonamides / pharmacology*
  • Treatment Outcome

Substances

  • Anti-HIV Agents
  • Carbamates
  • Furans
  • Organophosphates
  • Sulfonamides
  • HIV Protease
  • fosamprenavir