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Hydroxyurea-related toxicity in 3,411 patients with Ph'-negative MPN

  • Elisabetta Antonioli
  • , Paola Guglielmelli
  • , Lisa Pieri
  • , Mariachiara Finazzi
  • , Elisa Rumi
  • , Vincenzo Martinelli
  • , Nicola Vianelli
  • , Maria Luigia Randi
  • , Irene Bertozzi
  • , Valerio De Stefano
  • , Tommaso Za
  • , Elena Rossi
  • , Marco Ruggeri
  • , Elena Elli
  • , Rossella Cacciola
  • , Emma Cacciola
  • , Enrico Pogliani
  • , Francesco Rodeghiero
  • , Michele Baccarani
  • , Francesco Passamonti
  • Guido Finazzi, Alessandro Rambaldi, Alberto Bosi, Mario Cazzola, Tiziano Barbui, Alessandro M. Vannucchi
  • Azienda Ospedaliera Careggi
  • University of Florence
  • Ospedali Riuniti di Bergamo
  • University of Pavia
  • University of Naples Federico II
  • Alma Mater Studiorum University of Bologna
  • University of Padua
  • Azienda Sanitaria Ulss 6 Vicenza
  • University of Milan - Bicocca
  • University of Catania
  • AOU Fondazione Macchi

Risultato della ricerca: Contributo in rivistaArticolo

Abstract

Hydroxyurea (Hydroxycarbamide; HU) is commonly used for the long-term treatment of patients with Philadelphia-chromosome negative chronic myeloproliferative neoplasms (MPNs). It is considered a first-choice agent for the treatment of these disorders as underlined by the European Leukemia Net Consensus Conference [1], although it is formally approved for this indication in some countries only. The drug is reportedly well tolerated in the large majority of subjects, although systemic and/or localized toxicities have been reported. Consensus criteria for definition of "intolerance" to HU have been described;patients who develop intolerance are candidate for second-line therapy and, more recently, for investigational drugs. However, no epidemiologic information about the occurrence of the most clinically significant HU-associated adverse events is yet available. In this study, the authors report on a multicenter series of 3,411 patients who were treated with HU among which 184, accounting for 5% of total, developed significant drug-related toxicities. These data provide an estimate of the frequency and a detailed characterization of clinically significant HU-related toxicities; these information have relevance for the management of MPN patients who require second-line therapy after developing HU-related intolerance.
Lingua originaleInglese
pagine (da-a)552-554
Numero di pagine3
RivistaAmerican Journal of Hematology
Volume87
DOI
Stato di pubblicazionePubblicato - 2012

Keywords

  • MYELOPROLIFERATIVE NEOPLASM

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