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Iron chelation therapy for children with transfusion-dependent β-thalassemia: How young is too young?

  • Gian Luca Forni
  • , Antonis Kattamis
  • , Kevin H.M. Kuo
  • , Aurelio Maggio
  • , Sujit Sheth
  • , Ali T. Taher
  • , Vip Viprakasit
  • ForAnemia Foundation
  • University of Athens
  • University of Toronto
  • AOOR Villa Sofia-V. Cervello
  • Weill Cornell Medicine
  • American University of Beirut

Research output: Contribution to journalReview articlepeer-review

9 Citations (Scopus)

Abstract

In this review, we provide a summary of evidence on iron overload in young children with transfusion-dependent β-thalassemia (TDT) and explore the ideal timing for intervention. Key data from clinical trials and observational studies of the three available iron chelators deferoxamine, deferiprone, and deferasirox are also evaluated for inclusion of subsets of young children, especially those less than 6 years of age. Evidence on the efficacy and safety of iron chelation therapy for children ≥2 years of age with transfusional iron overload is widely available. New data exploring the risks and benefits of early-start iron chelation in younger patients with minimal iron overload are also emerging.

Original languageEnglish
Article numbere31035
JournalPediatric Blood and Cancer
Volume71
Issue number8
DOIs
Publication statusPublished - Aug 2024

Keywords

  • ferritin
  • heart
  • iron chelation
  • iron overload
  • liver
  • thalassemia

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