Simple jQuery Dropdowns
Please use this identifier to cite or link to this item: http://repository.li.mahidol.ac.th/dspace/handle/123456789/29730
Title: Tailoring iron chelation by iron intake and serum ferritin: The prospective EPIC study of deferasirox in 1744 patients with transfusion-dependent anemias
Authors: Maria Domenica Cappellini
John Porter
Amal El-Beshlawy
Chi Kong Li
John F. Seymour
Mohsen Elalfy
Norbert Gattermann
Stéphane Giraudier
Jong Wook Lee
Lee Lee Chan
Kai Hsin Lin
Christian Rose
Ali Taher
Swee Lay Thein
Vip Viprakasit
Dany Habr
Gabor Domokos
Bernard Roubert
Antonis Kattamis
Universita degli Studi di Milano
UCL
Cairo University
Prince of Wales Hospital Hong Kong
Peter Maccallum Cancer Centre
Ain Shams University
Heinrich Heine Universitat
Hopital Henri Mondor
The Catholic University of Korea
University of Malaya Medical Centre
National Taiwan University Hospital
Hopital Saint-Vincent-de-Paul
American University of Beirut
King's College London
Mahidol University
Novartis Pharmaceuticals Corporation
Novartis International AG
University of Athens
Keywords: Medicine
Issue Date: 1-Apr-2010
Citation: Haematologica. Vol.95, No.4 (2010), 557-566
Abstract: Background: Following a clinical evaluation of deferasirox (Exjade®) it was concluded that, in addition to baseline body iron burden, ongoing transfusional iron intake should be considered when selecting doses. The 1-year EPIC study, the largest ever investigation conducted for an iron chelator, is the first to evaluate whether fixed starting doses of deferasirox, based on transfusional iron intake, with dose titration guided by serum ferritin trends and safety markers, provides clinically acceptable chelation in patients (aged ≥2 years) with transfusional hemosiderosis from various types of anemia. Design and Methods: The recommended initial dose was 20 mg/kg/day for patients receiving 2-4 packed red blood cell units/month and 10 or 30 mg/kg/day was recommended for patients receiving less or more frequent transfusions, respectively. Dose adjustments were based on 3-month serum ferritin trends and continuous assessment of safety markers. The primary efficacy end-point was change in serum ferritin after 52 weeks compared with baseline. Results: The 1744 patients enrolled had the following conditions; thalassemia (n=1115), myelodysplastic syndromes (n=341), aplastic anemia (n=116), sickle cell disease (n=80), rare anemias (n=43) and other transfused anemias (n=49). Overall, there was a significant reduction in serum ferritin from baseline (-264 ng/mL; P<0.0001), reflecting dosage adjustments and ongoing iron intake. The most common (>5%) adverse events were gastrointestinal disturbances (28%) and skin rash (10%). Conclusions: Analysis of this large, prospectively collected data set confirms the response to chelation ther- apy across various anemias, supporting initial deferasirox doses based on transfusional iron intake, with subsequent dose titration guided by trends in serum ferritin and safety markers (clinicaltrials.gov identifier: NCT00171821). © 2010 Ferrata Storti Foundation.
URI: https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=77950682176&origin=inward
http://repository.li.mahidol.ac.th/dspace/handle/123456789/29730
ISSN: 15928721
03906078
Appears in Collections:Scopus 2006-2010

Files in This Item:
There are no files associated with this item.


Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.