Population pharmacokinetics of abacavir and lamivudine in severely malnourished human immunodeficiency virus-infected children in relation to treatment outcomes

Br J Clin Pharmacol. 2019 Sep;85(9):2066-2075. doi: 10.1111/bcp.13998. Epub 2019 Jul 7.

Abstract

Aims: Describe the pharmacokinetics (PK) of the antiretroviral drugs abacavir and lamivudine in malnourished paediatric patients and relate to viral load outcomes after 12 and 48 weeks of treatment.

Methods: Severely malnourished human immunodeficiency virus-infected children were randomized to early (within 14 days) or delayed (after nutritional recovery) initiation of antiretroviral treatment (ART) using World Health Organization weight-band dosages. Abacavir and lamivudine concentrations were measured as a secondary objective on day 1 and day 14 and patients were followed-up to week 48. Population PK of abacavir and lamivudine were described using NONMEM.

Results: In total, 623 abacavir and 627 lamivudine concentrations were collected from 75 paediatric patients aged 0.1-10.8 (median 1.4) years. Abacavir PK was described by a 2-compartment model, patients randomized to early ART showed increased bioavailability of 31%. Apparent clearance (CL/F, L/h/7 kg) of abacavir increased from day 1 to day 14 from 3.33 (95% confidence interval 2.71-4.12) to 5.86 (95% confidence interval 4.78-7.3). A 1-compartment model described lamivudine PK, variability on CL/F was explained by maturation with age, with age at half-matured CL/F being 4 months. For both drugs allometrically scaled total body weight was related to CL/F and apparent volume of distribution. PK exposure did not correlate with virological outcomes or death at 12 or 48 weeks.

Conclusion: Increases in Abacavir's CL/F between day 1 to day 14, bioavailability and PK variability with early start of ART was found in this cohort of severely malnourished children; however, these changes did not influence virological outcomes. The study supports the use of weight-band dosage tables.

Keywords: abacavir; children; human immunodeficiency virus; lamivudine; population pharmacokinetics; severe acute malnutrition.

Publication types

  • Randomized Controlled Trial
  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Anti-HIV Agents / administration & dosage
  • Anti-HIV Agents / adverse effects
  • Anti-HIV Agents / pharmacokinetics*
  • Biological Availability
  • Body Weight
  • Child
  • Child Nutrition Disorders / diagnosis
  • Child Nutrition Disorders / etiology
  • Child Nutrition Disorders / metabolism*
  • Child Nutrition Disorders / rehabilitation
  • Child, Preschool
  • Dideoxynucleosides / administration & dosage
  • Dideoxynucleosides / adverse effects
  • Dideoxynucleosides / pharmacokinetics*
  • Dose-Response Relationship, Drug
  • Drug Administration Schedule
  • Drug Dosage Calculations
  • Female
  • Follow-Up Studies
  • HIV / isolation & purification
  • HIV Infections / blood
  • HIV Infections / complications
  • HIV Infections / drug therapy*
  • HIV Infections / mortality
  • Humans
  • Infant
  • Lamivudine / administration & dosage
  • Lamivudine / adverse effects
  • Lamivudine / pharmacokinetics*
  • Male
  • Models, Biological
  • Nutritional Support
  • Severity of Illness Index
  • South Africa / epidemiology
  • Time Factors
  • Time-to-Treatment
  • Treatment Outcome
  • Viral Load

Substances

  • Anti-HIV Agents
  • Dideoxynucleosides
  • Lamivudine
  • abacavir