Literature DB >> 18274978

Ethical issues and risk/benefit assessment of iron chelation therapy: advances with deferiprone/deferoxamine combinations and concerns about the safety, efficacy and costs of deferasirox.

George J Kontoghiorghes1.   

Abstract

New developments in the area of iron and other metal metabolism and toxicity and the effects and uses of chelators have been presented at the 16th International Conference on Chelation (ICOC), Limassol, Cyprus in October 2006. Marketing practices by pharmaceutical companies, contradictory policies by regulatory authorities and ineffective policies by health authorities deprive thousands of thalassemia and other transfused patients of life saving iron chelating drugs and of efficacious chelation treatments. Thousands of patients were using deferasirox (DFRA) worldwide a few months after the European Union (EU) authorities, and about 1 year after the Food and Drugs Administration (FDA), proceeded to its accelerated approval with no sufficient evidence that the drug was efficacious, especially for clearing excess cardiac iron, and also safe. Cases of fatal, acute, irreversible renal and liver failure, fatal agranulocytosis and other toxicities have recently been reported with DFRA. The FDA has not yet approved deferiprone (L1) depriving thousands of patients of potentially life saving treatment. The high cost of DFRA at 60 euros/g, L1 at 5.5 euros/g and deferoxamine (DFO) at 8.3 euros/g, diminishes the prospects of universal chelation therapy, especially for patients in developing countries. The safety and efficacy record of L1, DFO, and their combination in particular, appear to provide universal solutions in the treatment of transfusional iron overload, and also in reducing mortality because of their ability to clear rapidly and effectively excess cardiac iron.

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Year:  2008        PMID: 18274978     DOI: 10.1080/03630260701726533

Source DB:  PubMed          Journal:  Hemoglobin        ISSN: 0363-0269            Impact factor:   0.849


  9 in total

1.  New developments and controversies in iron metabolism and iron chelation therapy.

Authors:  Christina N Kontoghiorghe; George J Kontoghiorghes
Journal:  World J Methodol       Date:  2016-03-26

Review 2.  World health dilemmas: Orphan and rare diseases, orphan drugs and orphan patients.

Authors:  Christina N Kontoghiorghe; Nicholas Andreou; Katerina Constantinou; George J Kontoghiorghes
Journal:  World J Methodol       Date:  2014-09-26

Review 3.  The relevance of iron overload and the appropriateness of iron chelation therapy for patients with myelodysplastic syndromes: a dialogue and debate.

Authors:  David P Steensma
Journal:  Curr Hematol Malig Rep       Date:  2011-06       Impact factor: 3.952

Review 4.  Transition of Thalassaemia and Friedreich ataxia from fatal to chronic diseases.

Authors:  Annita Kolnagou; Christina N Kontoghiorghe; George J Kontoghiorghes
Journal:  World J Methodol       Date:  2014-12-26

5.  Refractive errors and ocular biometry components in thalassemia major patients.

Authors:  Samira Heydarian; Reza Jafari; Hosein Karami
Journal:  Int Ophthalmol       Date:  2015-12-08       Impact factor: 2.031

6.  TLc-A, the leading nanochelating-based nanochelator, reduces iron overload in vitro and in vivo.

Authors:  Somayeh Kalanaky; Maryam Hafizi; Sepideh Safari; Kazem Mousavizadeh; Mahboubeh Kabiri; Alireza Farsinejad; Saideh Fakharzadeh; Mohammad Hassan Nazaran
Journal:  Int J Hematol       Date:  2016-02-01       Impact factor: 2.490

Review 7.  Efficacy and safety of iron-chelation therapy with deferoxamine, deferiprone, and deferasirox for the treatment of iron-loaded patients with non-transfusion-dependent thalassemia syndromes.

Authors:  Christina N Kontoghiorghe; George J Kontoghiorghes
Journal:  Drug Des Devel Ther       Date:  2016-01-29       Impact factor: 4.162

8.  Questioning Established Theories and Treatment Methods Related to Iron and Other Metal Metabolic Changes, Affecting All Major Diseases and Billions of Patients.

Authors:  George J Kontoghiorghes
Journal:  Int J Mol Sci       Date:  2022-01-25       Impact factor: 5.923

9.  Ocular abnormalities in multi-transfused beta-thalassemia patients.

Authors:  Reza Jafari; Samira Heydarian; Hosein Karami; Mohammad Momeni Shektaei; Kiumars Noruzpour Dailami; Ahmad Ahmadzadeh Amiri; Majid Reza Sheikh Rezaee; Asad Allah Farrokh Far
Journal:  Indian J Ophthalmol       Date:  2015-09       Impact factor: 1.848

  9 in total

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