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Impact of 2016 WHO diagnosis of early and overt primary myelofibrosis on presentation and outcome of 232 patients treated with ruxolitinib
Authors:Francesca Palandri  Giuseppe A Palumbo  Elisabetta Abruzzese  Alessandra Iurlo  Nicola Polverelli  Elena Elli  Massimiliano Bonifacio  Micaela Bergamaschi  Bruno Martino  Mario Tiribelli  Giulia Benevolo  Alessia Tieghi  Nicola Sgherza  Alessandro Isidori  Gianni Binotto  Monica Crugnola  Florian Heidel  Francesco Cavazzini  Costanza Bosi  Giuseppe Auteri  Daniele Cattaneo  Robin Fo  Roberto M Lemoli  Antonio Cuneo  Mauro Krampera  Daniela Bartoletti  Michele Cavo  Nicola Vianelli  Massimo Breccia  Roberto Latagliata
Institution:Francesca Palandri,Giuseppe A. Palumbo,Elisabetta Abruzzese,Alessandra Iurlo,Nicola Polverelli,Elena Elli,Massimiliano Bonifacio,Micaela Bergamaschi,Bruno Martino,Mario Tiribelli,Giulia Benevolo,Alessia Tieghi,Nicola Sgherza,Alessandro Isidori,Gianni Binotto,Monica Crugnola,Florian Heidel,Francesco Cavazzini,Costanza Bosi,Giuseppe Auteri,Daniele Cattaneo,Robin Foà,Roberto M. Lemoli,Antonio Cuneo,Mauro Krampera,Daniela Bartoletti,Michele Cavo,Nicola Vianelli,Massimo Breccia,Roberto Latagliata
Abstract:The 2016 WHO criteria identified early primary myelofibrosis (PMF) as an individual entity with milder clinical features and better outcome compared with overt PMF. Here, we compared early and overt PMF patients treated with ruxolitinib in terms of baseline clinical/laboratory characteristics, response, and toxicity to treatment. We observed that early‐PMF patients achieve better and more stable spleen and symptoms responses, with significantly lower rates of hematological toxicities. No differences in overall and leukemia‐free survival were detected between the two cohorts. The application of 2016 WHO criteria is crucial to identify those PMF patients who deserve a stricter monitoring during treatment.
Keywords:MYELOFIBROSIS  RUXOLITINIB  EARLY PMF  OVERT PMF
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