Neutropenia in Children Treated with Deferiprone or Deferasirox: A Report of the Largest Randomized Trial of Oral Chelators in Transfusion-Dependent Pediatric Patients

Introduction: Agranulocytosis/severe neutropenia is an established adverse event during deferiprone (DFP) use. Less is known about milder episodes, which are frequently transient despite continuous deferiprone use. To provide further insight into this topic, we compared the incidence of neutropenia...

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Veröffentlicht in:Blood 2019-11, Vol.134 (Supplement_1), p.3552-3552
Hauptverfasser: Tricta, Fernando, Felisi, Mariagrazia, Della Pasqua, Oscar, El-Beshlawy, Amal, Hassab, Hoda, Kattamis, Antonis, Kreka, Manika, Reggiardo, Giorgio, Sherief, Laila Metwally, Spino, Michael, Tempesta, Bianca, Tsang, Yu-Chung, Ceci, Adriana
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Sprache:eng
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Zusammenfassung:Introduction: Agranulocytosis/severe neutropenia is an established adverse event during deferiprone (DFP) use. Less is known about milder episodes, which are frequently transient despite continuous deferiprone use. To provide further insight into this topic, we compared the incidence of neutropenia during DFP or deferasirox (DFX) treatment in the randomized Deferiprone Evaluation in Paediatrics (DEEP-2) trial, where blood neutrophil count was regularly monitored in patients randomized to be treated with DFP or DFX. Methods: DEEP-2 was a multicenter, randomized, 12-month, open-label trial comparing DFP vs DFX in pediatric (
ISSN:0006-4971
1528-0020
DOI:10.1182/blood-2019-127933