Low initial trough plasma concentrations of lopinavir are associated with an impairment of virological response in an unselected cohort of HIV-1-infected patients

HIV Med. 2006 Apr;7(3):197-9. doi: 10.1111/j.1468-1293.2006.00354.x.

Abstract

Objectives: The relationship between lopinavir trough plasma concentration at baseline and virological efficacy 3 months after the beginning of the therapy was investigated in an unselected cohort of HIV-1-infected patients

Methods: According to initial trough lopinavir plasma level, patients were classified into three groups: the subtherapeutic group (<3 mg/L, n=18), the therapeutic group (between 3 and 8 mg/L, n=50) and the toxic group (>8 mg/L, n=16). The virological response after 3 months of lopinavir treatment, defined as a viral load <200 HIV-1 RNA copies/mL, was compared amongst these groups.

Results: The virological response was significantly different (P<0.05) between the subtherapeutic group (22.% of patients with viral load<200 copies/mL) and the other groups (56.0% of patients with a viral load<200 copies/mL in the therapeutic group and 56.2% in the toxic group).

Conclusions: A lower virological efficacy should be expected for experienced or naive patients with plasma trough lopinavir concentrations<3 mg/L at the beginning of treatment.

Publication types

  • Comparative Study

MeSH terms

  • Adult
  • Chi-Square Distribution
  • Drug Administration Schedule
  • Female
  • HIV Infections / blood*
  • HIV Infections / drug therapy
  • HIV Protease Inhibitors / blood*
  • HIV Protease Inhibitors / therapeutic use*
  • HIV-1*
  • Humans
  • Lopinavir
  • Male
  • Middle Aged
  • Pyrimidinones / blood*
  • Pyrimidinones / therapeutic use*
  • Retrospective Studies
  • Ritonavir / therapeutic use
  • Time Factors
  • Treatment Outcome
  • Viral Load

Substances

  • HIV Protease Inhibitors
  • Pyrimidinones
  • Lopinavir
  • Ritonavir