American journal of hematology · 2012
Hydroxyurea-related toxicity in 3,411 patients with Ph'-negative MPN.
СтатьяМногоцентровое исследованиеПоддержка исследования: вне правительства СШАНазвание и аннотация: Перевод пока не подготовлен
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Antonioli Elisabetta, Guglielmelli Paola, Pieri Lisa, Finazzi MariaChiara, Rumi Elisa, Martinelli Vincenzo, Vianelli Nicola, Luigia Randi Maria, Bertozzi Irene, De Stefano Valerio, Za Tommaso, Rossi Elena, Ruggeri Marco, Elli Elena, Cacciola Rossella, Cacciola Emma, Pogliani Enrico, Rodeghiero Francesco, Baccarani Michele, Passamonti Francesco, Finazzi Guido, Rambaldi Alessandro, Bosi Alberto, Cazzola Mario, Barbui Tiziano, Vannucchi Alessandro M, AGIMM Investigators
Аннотация
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.