Elevated plasma ferritin and busulfan pharmacodynamics during high-dose chemotherapy regimens in children with malignant solid tumors

Clin Pharmacol Ther. 2007 Oct;82(4):402-9. doi: 10.1038/sj.clpt.6100168. Epub 2007 Mar 28.

Abstract

Hepatic veno-occlusive disease (HVOD) is a frequent complication during hematopoietic stem-cell transplantation (HSCT). A strong relationship has been demonstrated between busulfan exposure and HVOD for busulfan-cyclophosphamide and allogeneic HSCT in adults. Busulfan disposition after the first intake was studied in 77 children treated for solid malignancies with high-dose busulfan-containing regimens and autologous HSCT. Busulfan was combined with cyclophosphamide and melphalan (n=30), melphalan (n=27), and thiotepa (n=20). No relationship was observed between busulfan exposure and HVOD. In contrast, plasma ferritin at baseline was higher in patients with HVOD (750 ng/ml (20-3,110)) compared with those without HVOD (189 ng/ml (8-3,967), P=0.012). Multivariate analysis showed that a ferritin level exceeding 300 ng/ml was the only risk factor for HVOD with an odds ratio of 4.0 (confidence interval 95% (1.5-11.2), P=0.0071). A high ferritin level at baseline was explained by the diagnosis of neuroblastoma, related treatments and transfusions.

Publication types

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

MeSH terms

  • Adolescent
  • Antineoplastic Combined Chemotherapy Protocols / adverse effects
  • Antineoplastic Combined Chemotherapy Protocols / pharmacokinetics
  • Antineoplastic Combined Chemotherapy Protocols / therapeutic use*
  • Busulfan / administration & dosage
  • Busulfan / adverse effects
  • Busulfan / pharmacokinetics
  • Child
  • Child, Preschool
  • Cyclophosphamide / administration & dosage
  • Female
  • Ferritins / blood*
  • Hematopoietic Stem Cell Transplantation / adverse effects*
  • Hepatic Veno-Occlusive Disease / blood
  • Hepatic Veno-Occlusive Disease / epidemiology
  • Hepatic Veno-Occlusive Disease / etiology*
  • Humans
  • Incidence
  • Infant
  • Iron / blood
  • Male
  • Melphalan / administration & dosage
  • Neoplasms / blood
  • Neoplasms / drug therapy*
  • Neoplasms / surgery
  • Odds Ratio
  • Prospective Studies
  • Risk Assessment
  • Risk Factors
  • Severity of Illness Index
  • Thiotepa / administration & dosage
  • Transferrin / metabolism
  • Transplantation, Homologous
  • Treatment Outcome

Substances

  • Transferrin
  • Cyclophosphamide
  • Ferritins
  • Thiotepa
  • Iron
  • Busulfan
  • Melphalan