| Literature DB >> 26898196 |
Alberto Alvarez-Larrán1, Ana Kerguelen2, Juan C Hernández-Boluda3, Manuel Pérez-Encinas4, Francisca Ferrer-Marín5, Abelardo Bárez6, Joaquín Martínez-López7, Beatriz Cuevas8, M Isabel Mata9, Valentín García-Gutiérrez10, Pilar Aragües11, Sara Montesdeoca1, Carmen Burgaleta12, Gonzalo Caballero13, J Angel Hernández-Rivas14, M Antonia Durán15, M Teresa Gómez-Casares16, Carles Besses1.
Abstract
The clinical significance of resistance/intolerance to hydroxycarbamide (HC) was assessed in a series of 890 patients with polycythaemia vera (PV). Resistance/intolerance to HC was recorded in 137 patients (15·4%), consisting of: need for phlebotomies (3·3%), uncontrolled myeloproliferation (1·6%), failure to reduce massive splenomegaly (0·8%), development of cytopenia at the lowest dose of HC to achieve a response (1·7%) and extra-haematological toxicity (9%). With a median follow-up of 4·6 years, 99 patients died, resulting in a median survival of 19 years. Fulfilling any of the resistance/intolerance criteria had no impact on survival but when the different criteria were individually assessed, an increased risk of death was observed in patients developing cytopenia [Hazard ratio (HR): 3·5, 95% confidence interval (CI): 1·5-8·3, P = 0·003]. Resistance/intolerance had no impact in the rate of thrombosis or bleeding. Risk of myelofibrotic transformation was significantly higher in those patients developing cytopenia (HR: 5·1, 95% CI: 1·9-13·7, P = 0·001) and massive splenomegaly (HR: 9·1, 95% CI: 2·3-35·9, P = 0·002). Cytopenia at the lowest dose required to achieve a response was also an independent risk factor for transformation to acute leukaemia (HR: 20·3, 95% CI: 5·4-76·5, P < 0·001). In conclusion, the unified definition of resistance/intolerance to HC delineates a heterogeneous group of PV patients, with those developing cytopenia being associated with an adverse outcome.Entities:
Keywords: hydroxycarbamide; myeloproliferative neoplasms; polycythaemia vera; resistance/intolerance; response criteria
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Year: 2015 PMID: 26898196 DOI: 10.1111/bjh.13886
Source DB: PubMed Journal: Br J Haematol ISSN: 0007-1048 Impact factor: 6.998