Deferasirox administration for the treatment of non-transfusional iron overload in patients with thalassaemia intermedia

Br J Haematol. 2010 Dec;151(5):504-8. doi: 10.1111/j.1365-2141.2010.08346.x. Epub 2010 Oct 18.

Abstract

Abnormal iron regulation in patients with thalassaemia intermedia may lead to iron overload even in the absence of transfusions. There are limited data on iron chelator use in patients with thalassaemia intermedia and no guidelines exist for the management of iron overload. We present data from 11 patients with thalassaemia intermedia treated with deferasirox (Exjade(®) , 10-20 mg/kg/d) for 24 months. Liver iron concentration and serum ferritin levels significantly decreased over the first 12 months (P = 0·005) and continued to decrease over the remainder of the study (P = 0·005). This small-scale study indicated that deferasirox may be suitable for controlling iron levels in patients with thalassaemia intermedia.

Publication types

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

MeSH terms

  • Adult
  • Benzoates / adverse effects
  • Benzoates / therapeutic use*
  • Deferasirox
  • Female
  • Ferritins / blood
  • Humans
  • Iron / metabolism
  • Iron Chelating Agents / adverse effects
  • Iron Chelating Agents / therapeutic use*
  • Iron Overload / diagnosis
  • Iron Overload / drug therapy*
  • Iron Overload / etiology
  • Iron Overload / metabolism
  • Liver / metabolism
  • Magnetic Resonance Imaging
  • Male
  • Treatment Outcome
  • Triazoles / adverse effects
  • Triazoles / therapeutic use*
  • Young Adult
  • beta-Thalassemia / complications*
  • beta-Thalassemia / metabolism

Substances

  • Benzoates
  • Iron Chelating Agents
  • Triazoles
  • Ferritins
  • Iron
  • Deferasirox