Literature DB >> 22176640

Deferasirox: pharmacokinetics and clinical experience.

Renzo Galanello1, Simona Campus, Raffaella Origa.   

Abstract

INTRODUCTION: Iron overload is an inevitable consequence of transfusion therapy for a variety of underlying anemias. Iron overload, without effective chelation, will lead to significant morbidity and mortality. Deferasirox (Exjade®) is an oral tridentate iron chelator used for reducing iron overload. AREAS COVERED: In addition to the pharmacokinetic and pharmacodynamic profile of deferasirox, this review examines the efficacy and safety data from pivotal studies with deferasirox in iron-overloaded patients with various anemias, including thalassemia, sickle cell disease and myelodysplastic syndromes. A qualitative literature search for deferasirox was performed using PubMed and recent key congress publications (EHA and ASH); key search terms were deferasirox, pharmacokinetic, pharmacodynamic, efficacy and safety. EXPERT OPINION: Based on the current available data, deferasirox treatment is effective with a clinically manageable safety profile although appropriate dosing according to the severity of iron burden and iron intake, together with the careful monitoring of laboratory parameters and adverse events, is recommended. However, despite advances made in the treatment of iron overload, some patients still do not respond adequately to iron chelators, and increased awareness, understanding and further research are still needed.

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Year:  2011        PMID: 22176640     DOI: 10.1517/17425255.2012.640674

Source DB:  PubMed          Journal:  Expert Opin Drug Metab Toxicol        ISSN: 1742-5255            Impact factor:   4.481


  9 in total

Review 1.  Opportunities for model-based precision dosing in the treatment of sickle cell anemia.

Authors:  Min Dong; Tomoyuki Mizuno; Alexander A Vinks
Journal:  Blood Cells Mol Dis       Date:  2017-08-09       Impact factor: 3.039

Review 2.  Deferasirox: a review of its use for chronic iron overload in patients with non-transfusion-dependent thalassaemia.

Authors:  Matt Shirley; Greg L Plosker
Journal:  Drugs       Date:  2014-06       Impact factor: 9.546

3.  Clinically approved iron chelators influence zebrafish mortality, hatching morphology and cardiac function.

Authors:  Jasmine L Hamilton; Azadeh Hatef; Muhammad Imran ul-Haq; Neelima Nair; Suraj Unniappan; Jayachandran N Kizhakkedathu
Journal:  PLoS One       Date:  2014-10-16       Impact factor: 3.240

4.  Polymeric nanocarriers for the treatment of systemic iron overload.

Authors:  Jasmine L Hamilton; Jayachandran N Kizhakkedathu
Journal:  Mol Cell Ther       Date:  2015-03-24

5.  Jadenu® Substituting Exjade® in Iron Overloaded β-Thalassemia Major (BTM) Patients: A Preliminary Report of the Effects on the Tolerability, Serum Ferritin Level, Liver Iron Concentration and Biochemical Profiles.

Authors:  Mohamed A Yassin; Ashraf T Soliman; Vincenzo De Sanctis; Radwa M Hussein; Randa Al-Okka; Nancy Kassem; Rula Ghasoub; Ahmed Basha; Abdulqadir J Nashwan; Ahmad M Adel
Journal:  Mediterr J Hematol Infect Dis       Date:  2018-11-01       Impact factor: 2.576

6.  Genetic Modifiers at the Crossroads of Personalised Medicine for Haemoglobinopathies.

Authors:  Coralea Stephanou; Stella Tamana; Anna Minaidou; Panayiota Papasavva; Marina Kleanthous; Petros Kountouris
Journal:  J Clin Med       Date:  2019-11-09       Impact factor: 4.241

7.  Transfusion-dependent low-risk myelodysplastic patients receiving deferasirox: Long-term follow-up.

Authors:  Salvatore Improta; Maria Rosaria Villa; Antonio Volpe; Angela Lombardi; Paola Stiuso; Nicola Cantore; Lucia Mastrullo
Journal:  Oncol Lett       Date:  2013-10-10       Impact factor: 2.967

8.  Safety and tolerability of deferasirox in pediatric hematopoietic stem cell transplant recipients: one facility's five years' experience of chelation treatment.

Authors:  Natalia Maximova; Massimo Gregori; Roberto Simeone; Aurelio Sonzogni; Giulia Boz; Carmen Fucile; Valeria Marini; Antonietta Martelli; Francesca Mattioli
Journal:  Oncotarget       Date:  2017-06-28

Review 9.  Atrial Fibrillation in β-Thalassemia: Overview of Mechanism, Significance and Clinical Management.

Authors:  Michele Malagù; Federico Marchini; Alessio Fiorio; Paolo Sirugo; Stefano Clò; Elisa Mari; Maria Rita Gamberini; Claudio Rapezzi; Matteo Bertini
Journal:  Biology (Basel)       Date:  2022-01-17
  9 in total

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