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Use of Deferasirox Film-Coated Tablets in Pediatric Patients with Transfusion Dependent Thalassemia: A Single Center Experience

SIMPLE SUMMARY: Thalassemia is a hereditary anemia characterized by defect in hemoglobin synthesis. Patients with severe forms of the disease require regular blood transfusions, as well as iron chelation. Available chelators have demonstrated long-term efficacy and safety, but present various limita...

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Detalles Bibliográficos
Autores principales: Adramerina, Alkistis, Printza, Nikoleta, Hatzipantelis, Emmanouel, Symeonidis, Symeon, Tarazi, Labib, Teli, Aikaterini, Economou, Marina
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8869542/
https://www.ncbi.nlm.nih.gov/pubmed/35205113
http://dx.doi.org/10.3390/biology11020247
Descripción
Sumario:SIMPLE SUMMARY: Thalassemia is a hereditary anemia characterized by defect in hemoglobin synthesis. Patients with severe forms of the disease require regular blood transfusions, as well as iron chelation. Available chelators have demonstrated long-term efficacy and safety, but present various limitations. A new deferasirox film-coated tablet (DFX FCT) was designed to offer a more convenient mode of administration and better tolerability. The present study aimed to assess the efficacy and safety of DFX FCT in thalassemic pediatric patients. DFX FCT proved safe for older patients, but demonstrated increased frequency of adverse events in younger patients, resulting in drug discontinuation. As for efficacy, DFX FCT succeeded in maintaining a stable iron load, though it required use of relatively high doses. ABSTRACT: Thalassemic syndromes are characterized by clinical heterogenicity. For severe disease forms, lifelong blood transfusions remain the mainstay of therapy, while iron overload monitoring and adequate chelation treatment are required in order to ensure effective disease management. Compared to previous chelators, the new deferasirox film-coated tablet (DFX FCT) is considered to offer a more convenient and well-tolerated treatment scheme, aiming at better treatment-related and patient-related outcomes. The present study’s objective was to prospectively evaluate the safety and efficacy of DFX FCT in children and adolescents with transfusion-dependent thalassemia. Data collected included patient demographics, hematology and biochemistry laboratory work up, magnetic resonance imaging of heart and liver for iron load, as well as ophthalmological and audiological examination prior to and a year following drug administration. Study results confirmed DFX FCT safety in older children in a manner similar to adults, but demonstrated increased frequency of adverse events in younger patients, mainly, involving liver function. With regards to efficacy, study results confirmed the preventive role of DFX FCT in iron loading of liver and heart, however, higher doses than generally recommended were required in order to ensure adequate chelation.