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Article

Overview of Current Chelation Practices

Department of Pediatric Hematology, Ege University Medical School, Izmir, Turkey
Thalass. Rep. 2011, 1(s2), e10; https://doi.org/10.4081/thal.2011.s2.e10
Submission received: 1 December 2011 / Revised: 15 December 2011 / Accepted: 28 December 2011 / Published: 30 December 2011

Abstract

Deferoxamine (DFO) is reference standard therapy for transfusional iron overload since the 1980s. Although it is a highly effective iron chelator, the compliance problem to subcutaneous administration of DFO remains as the major problem. The oral chelator Deferiprone (DFP) has no marketing licence in North America, however, it has been licensed in India since 1994 and the European Union (EU) granted marketing approval for DFP in 1999, specifically for patients with thalassemia major when DFO is inadequate, intolerable or unacceptable. There are still limited data available on the use of DFP in children between 6 and 10 years of age, and no data on DFP use in children under 6 years of age. Subsequently the oral chelator Deferasirox (DFX) was approved by FDA and EMA for the treatment of patients with transfusional iron overload -older than 2 years of age- as first line therapy, in 2005 and 2006 respectively. The primary objective of iron chelation is to maintain body iron at safe levels at all times but once iron is accumulated, the objective of iron chelation is to reduce tissue iron to safe levels which is a slow process. The chelation regimen, dose and frequency of administration, of the chelator(s) are mainly determined based on body iron burden, presence of myocardial iron and the transfusional iron loading rate. A proper monitoring of chelation is of importance for measuring the response rate to a particular regimen and providing dose adjustments to enhance chelation efficacy and to avoid toxicity. Efficacy of a chelation regimen may exhibit individual variability resulting from factors such as absorbtion and metabolism of the chelator. Tolerability and compliance are also individual variables effecting the response to chelation. Understanding of advantages and limitations of chelators, accurately determining chelation needs of patients with iron overload and designing individualized chelation regimens with less toxicity but optimum efficacy, should provide long-term survival and quality of life for patients with iron loading anemias. The goal of this review is to summarize current concepts in iron chelation therapies based on the considerable amount of prospective data obtained by clinical studies.
Keywords: thalassemia; oral chelators thalassemia; oral chelators

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MDPI and ACS Style

Aydinok, Y. Overview of Current Chelation Practices. Thalass. Rep. 2011, 1, e10. https://doi.org/10.4081/thal.2011.s2.e10

AMA Style

Aydinok Y. Overview of Current Chelation Practices. Thalassemia Reports. 2011; 1(s2):e10. https://doi.org/10.4081/thal.2011.s2.e10

Chicago/Turabian Style

Aydinok, Y. 2011. "Overview of Current Chelation Practices" Thalassemia Reports 1, no. s2: e10. https://doi.org/10.4081/thal.2011.s2.e10

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