Clinical relevance of deferasirox trough levels in β-thalassemia patients

Clin Exp Pharmacol Physiol. 2018 Feb;45(2):213-216. doi: 10.1111/1440-1681.12879. Epub 2017 Dec 4.

Abstract

We evaluated the role of deferasirox therapeutic drug monitoring in order to avoid toxicity or treatment failure. Plasma concentrations, measured between two consecutive liver iron determinations, were determined at the end of dosing interval. Fifty-four β-thalassemic adult patients were enrolled: 50% were males; median age was 32.3 years (IQR 19.1-41.7 years) and median body mass index was 22.25 kg/m2 (IQR 20.24-23.75 kg/m2 ). The mean deferasirox dose was 28.6 ± 6.3 mg/kg/d and mean plasma concentration was 17.3 ± 16.8 μg/mL. Drug levels showed lower results in males. Deferasirox concentration was significantly correlated with serum creatinine levels (P = .01) and serum ferritin (P < .0001). The assessment of deferasirox therapeutic drug monitoring could help clinicians to predict patient responses and to optimize the therapy.

Keywords: creatinine; ferritin; iron overload; therapeutic drug monitoring; β-thalassemia.

Publication types

  • Letter

MeSH terms

  • Adult
  • Cohort Studies
  • Deferasirox / pharmacokinetics*
  • Deferasirox / therapeutic use*
  • Dose-Response Relationship, Drug
  • Female
  • Humans
  • Iron Chelating Agents / pharmacokinetics
  • Iron Chelating Agents / therapeutic use
  • Iron Overload / drug therapy*
  • Male
  • Young Adult
  • beta-Thalassemia / drug therapy*

Substances

  • Iron Chelating Agents
  • Deferasirox