TY - JOUR
T1 - Hydroxyurea-related toxicity in 3,411 patients with Ph'-negative MPN
AU - Antonioli, Elisabetta
AU - Guglielmelli, Paola
AU - Pieri, Lisa
AU - Finazzi, Mariachiara
AU - Rumi, Elisa
AU - Martinelli, Vincenzo
AU - Vianelli, Nicola
AU - Luigia Randi, Maria
AU - Bertozzi, Irene
AU - De Stefano, Valerio
AU - Za, Tommaso
AU - Rossi, Elena
AU - Ruggeri, Marco
AU - Elli, Elena
AU - Cacciola, Rossella
AU - Cacciola, Emma
AU - Pogliani, Enrico
AU - Rodeghiero, Francesco
AU - Baccarani, Michele
AU - Passamonti, Francesco
AU - Finazzi, Guido
AU - Rambaldi, Alessandro
AU - Bosi, Alberto
AU - Cazzola, Mario
AU - Barbui, Tiziano
AU - Vannucchi, Alessandro M.
PY - 2012
Y1 - 2012
N2 - 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.
AB - 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.
KW - MYELOPROLIFERATIVE NEOPLASM
KW - MYELOPROLIFERATIVE NEOPLASM
UR - http://hdl.handle.net/10807/39615
U2 - 10.1002/ajh.23160
DO - 10.1002/ajh.23160
M3 - Article
SN - 0361-8609
VL - 87
SP - 552
EP - 554
JO - American Journal of Hematology
JF - American Journal of Hematology
ER -