Cyclophosphamide pharmacokinetics in children

Br J Clin Pharmacol. 1996 Jan;41(1):13-19. doi: 10.1111/j.1365-2125.1996.tb00153.x.

Abstract

1. Cyclophosphamide pharmacokinetics were measured in 38 children with cancer. 2. A high degree of inter-patient variation was seen in all pharmacokinetic parameters. Cyclophosphamide half-life varied between 1.1 and 16.8 h, clearance varied between 1.2 and 10.61 h-1 m-2 and volume of distribution varied between 0.26 and 1.48 1 kg-1. 3. The half-life of cyclophosphamide was prolonged at high dose levels (P = 0.008). 4. Children who had received prior treatment with dexamethasone showed a mean increase in clearance of 2.51 h-1 m-2 (P = 0.001) presumably as a result of CYP450 enzyme induction. 5. Treatment with allopurinol or chlorpromazine was associated with a significant increase in cyclophosphamide half-life (P < 0.001 in both cases). 6. Dose and concurrent treatment may influence cyclophosphamide metabolism in vivo and thus potentially alter the drugs therapeutic effect.

Publication types

  • Clinical Trial
  • Comparative Study
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adolescent
  • Age Factors
  • Antineoplastic Agents, Alkylating / pharmacokinetics*
  • Child
  • Child, Preschool
  • Cyclophosphamide / blood
  • Cyclophosphamide / pharmacokinetics*
  • Drug Interactions
  • Female
  • Half-Life
  • Humans
  • Infant
  • Male
  • Neoplasms / blood
  • Neoplasms / drug therapy

Substances

  • Antineoplastic Agents, Alkylating
  • Cyclophosphamide