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Comparison of NNRTI vs PI/r
Study Mexican: EFV vs LPV/r, in combination
with ZDV/3TC
Original article : J Acquir Immune Defic Syndr. 2010 Apr;53(5):582-8 - J Sierra-Madero
Last update : 05/01/2011

Dr Anton Pozniak
Chelsea and Westminster Hospital
London, UK

  • In this very advanced HIV-infected antiretroviral-naïve population with a median CD4 closed to 50/mm3, EFV was virologically superior to LPV/r BID, when combined with ZDV/3TC
  • EFV superiority was due to both a higher rate of virologic failure and of discontinuations due to adverse event in the LPV/r group
  • Limits
    • Single country study, limited sample size (underpowered)
    • LPV/r soft-gel capsules and high pill burden associated with low tolerability and poor adherence in advanced HIV disease
    • NRTI backbone: ZDV/3TC

Design :

Objective :

  • Non inferiority of EFV vs LPV/r at W48: % HIV RNA < 50 c/mL by intention
    to treat, missing equals failure, TLOVR analysis (lower margin of the 2-sided 95% CI for the difference =  - 12%)

Baseline characteristics, patient disposition and primary endpoint at W48 :

Secondary endpoints :

  • HIV RNA < 50 c/mL at W48 according to baseline CD4
    • Baseline CD4 < 100/mm3 : EFV > LPV/r (p = 0.03)
    • Baseline CD4 > 100/mm3 : virologic response to EFV and LPV/r not different (p = 0.11)
  • Similar CD4+ cell count increase in both groups
  • Incidence of grade 2 to 4 adverse events similar between groups: 68%
    • Significantly greater increase in triglyceride levels in LPV/r arm vs EFV (p < 0.01)
    • Changes in total cholesterol, HDL, and LDL similar between groups
  • At virologic failure, only few patients were genotyped:
    • LPV/r, N = 5/17: no PI resistance, NRTI resistance in 1
    • EFV, N = 3/7: NNRTI resistance in 3, NRTI resistance in 2

 

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