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Does erythropoietin have a role in the treatment of β-hemoglobinopathies?

Abstract
This review presents the indications and contraindications (pros and cons) for the potential use of erythropoietin (Epo) as a treatment in β-thalassemia and sickle cell anemia (SCA). Its high cost and route of administration (by injection) are obvious obstacles, especially in underdeveloped countries, where thalassemia is prevalent. We believe that from the data summarized in this review, the time has come to define, by studying in vitro and in vivo models, as well as by controlled clinical trials, the rationale for treating patients with various forms of thalassemia and SCA with Epo alone or in combination with other medications.
AuthorsEitan Fibach, Eliezer A Rachmilewitz
JournalHematology/oncology clinics of North America (Hematol Oncol Clin North Am) Vol. 28 Issue 2 Pg. 249-63 (Apr 2014) ISSN: 1558-1977 [Electronic] United States
PMID24589265 (Publication Type: Journal Article, Review)
CopyrightCopyright © 2014 Elsevier Inc. All rights reserved.
Chemical References
  • Erythropoietin
Topics
  • Anemia, Sickle Cell (drug therapy)
  • Drug Therapy, Combination
  • Erythropoietin (therapeutic use)
  • Hemoglobinopathies (drug therapy)
  • Humans
  • Treatment Outcome
  • beta-Thalassemia (drug therapy)

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