Literature DB >> 20950401

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

Vassilis Ladis1, Helen Berdousi, Efstathios Gotsis, Antonis Kattamis.   

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.
© 2010 Blackwell Publishing Ltd.

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Year:  2010        PMID: 20950401     DOI: 10.1111/j.1365-2141.2010.08346.x

Source DB:  PubMed          Journal:  Br J Haematol        ISSN: 0007-1048            Impact factor:   6.998


  13 in total

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Review 10.  Reducing the iron burden and improving survival in transfusion-dependent thalassemia patients: current perspectives.

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Journal:  J Blood Med       Date:  2016-08-08
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