[Evidence-based therapeutic drug monitoring of lopinavir]

Therapie. 2011 May-Jun;66(3):231-8. doi: 10.2515/therapie/2011034. Epub 2011 Aug 9.
[Article in French]

Abstract

The HIV protease inhibitor lopinavir presents a wide inter-individual variability related to liver and intestinal metabolism involving CYP3A. Published studies were analyzed to establish whether there is evidence that therapeutic drug monitoring of lopinavir could improve patient care. In naïve or pretreated HIV-infected patients, no relationship could be evidenced between virological efficacy and trough lopinavir concentration, most likely because concentrations are above inhibitory concentrations. Although data are limited, patients with elevated triglycerides and cholesterol had trough lopinavir concentrations >8 000 ng/mL. These data suggest that the level of evidence of interest of lopinavir therapeutic drug monitoring is may be recommended in some situations such as children, pregnant women, pretreated patients if the number of mutations is <5, when coadministration with drug with metabolizing enzyme inducing properties is warranted and toxicity.

Publication types

  • English Abstract
  • Review

MeSH terms

  • Adult
  • Anti-HIV Agents / adverse effects
  • Anti-HIV Agents / economics
  • Anti-HIV Agents / pharmacokinetics
  • Anti-HIV Agents / therapeutic use*
  • Child
  • Dose-Response Relationship, Drug
  • Drug Interactions
  • Drug Monitoring
  • Evidence-Based Medicine
  • Female
  • HIV Infections / drug therapy*
  • HIV Protease Inhibitors / adverse effects
  • HIV Protease Inhibitors / economics
  • HIV Protease Inhibitors / pharmacokinetics
  • HIV Protease Inhibitors / therapeutic use*
  • Humans
  • Lopinavir / adverse effects
  • Lopinavir / economics
  • Lopinavir / pharmacokinetics
  • Lopinavir / therapeutic use*
  • Pregnancy

Substances

  • Anti-HIV Agents
  • HIV Protease Inhibitors
  • Lopinavir