Deferasirox pharmacokinetics evaluation in a woman with hereditary haemochromatosis and heterozygous β-thalassaemia

Biomed Pharmacother. 2016 Dec:84:1510-1512. doi: 10.1016/j.biopha.2016.11.041. Epub 2016 Nov 20.

Abstract

We present the deferasirox pharmacokinetics evaluation of a female patient on iron chelation, for the interesting findings from her genetic background (hereditary haemochromatosis and heterozygous β-thalassaemia) and clinical history (ileostomy; iron overload from transfusions). Drug plasma concentrations were measured by an HPLC-UV validated method, before and after ileum resection. Area under deferasirox concentration curve over 24h (AUC) values were determined by the mixed log-linear rule, using Kinetica software. AUC was low also with high deferasirox dose as well as tolerability. Non invasive tissue iron quantification by magnetic resonance imaging or superconducting quantum interference device were prevented by a metal hip replacement. Good efficacy and normalisation of iron markers was obtained on long term. Therapeutic drug monitoring in patient in critical conditions may help to understand reasons for non response and set individualised treatment.

Keywords: Deferasirox; Dfx; Haemochromatosis; Ileostomy; Iron chelation; Iron overload.

Publication types

  • Case Reports

MeSH terms

  • Benzoates / blood*
  • Benzoates / pharmacokinetics
  • Benzoates / therapeutic use
  • Deferasirox
  • Female
  • Hemochromatosis / blood*
  • Hemochromatosis / drug therapy
  • Humans
  • Iron Chelating Agents / pharmacokinetics*
  • Iron Chelating Agents / therapeutic use
  • Middle Aged
  • Triazoles / blood*
  • Triazoles / pharmacokinetics
  • Triazoles / therapeutic use
  • beta-Thalassemia / blood*
  • beta-Thalassemia / drug therapy

Substances

  • Benzoates
  • Iron Chelating Agents
  • Triazoles
  • Deferasirox