Class-sparing regimens for initial treatment of HIV-1 infection. Academic Article uri icon

Overview

abstract

  • BACKGROUND: The use of either efavirenz or lopinavir-ritonavir plus two nucleoside reverse-transcriptase inhibitors (NRTIs) is recommended for initial therapy for patients with human immunodeficiency virus type 1 (HIV-1) infection, but which of the two regimens has greater efficacy is not known. The alternative regimen of lopinavir-ritonavir plus efavirenz may prevent toxic effects associated with NRTIs. METHODS: In an open-label study, we compared three regimens for initial therapy: efavirenz plus two NRTIs (efavirenz group), lopinavir-ritonavir plus two NRTIs (lopinavir-ritonavir group), and lopinavir-ritonavir plus efavirenz (NRTI-sparing group). We randomly assigned 757 patients with a median CD4 count of 191 cells per cubic millimeter and a median HIV-1 RNA level of 4.8 log10 copies per milliliter to the three groups. RESULTS: At a median follow-up of 112 weeks, the time to virologic failure was longer in the efavirenz group than in the lopinavir-ritonavir group (P=0.006) but was not significantly different in the NRTI-sparing group from the time in either of the other two groups. At week 96, the proportion of patients with fewer than 50 copies of plasma HIV-1 RNA per milliliter was 89% in the efavirenz group, 77% in the lopinavir-ritonavir group, and 83% in the NRTI-sparing group (P=0.003 for the comparison between the efavirenz group and the lopinavir-ritonavir group). The groups did not differ significantly in the time to discontinuation because of toxic effects. At virologic failure, antiretroviral resistance mutations were more frequent in the NRTI-sparing group than in the other two groups. CONCLUSIONS: Virologic failure was less likely in the efavirenz group than in the lopinavir-ritonavir group. The virologic efficacy of the NRTI-sparing regimen was similar to that of the efavirenz regimen but was more likely to be associated with drug resistance. (ClinicalTrials.gov number, NCT00050895 [ClinicalTrials.gov].).

authors

  • Gulick, Roy M
  • Riddler, Sharon A
  • Haubrich, Richard
  • DiRienzo, A Gregory
  • Peeples, Lynne
  • Powderly, William G
  • Klingman, Karin L
  • Garren, Kevin W
  • George, Tania
  • Rooney, James F
  • Brizz, Barbara
  • Lalloo, Umesh G
  • Murphy, Robert L
  • Swindells, Susan
  • Havlir, Diane
  • Mellors, John W

publication date

  • May 15, 2008

Research

keywords

  • Benzoxazines
  • HIV Infections
  • HIV Protease Inhibitors
  • HIV-1
  • Pyrimidinones
  • Reverse Transcriptase Inhibitors
  • Ritonavir

Identity

PubMed Central ID

  • PMC3885902

Scopus Document Identifier

  • 43549094732

Digital Object Identifier (DOI)

  • 10.1056/NEJMoa074609

PubMed ID

  • 18480202

Additional Document Info

volume

  • 358

issue

  • 20