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Ruxolitinib in elderly patients with myelofibrosis: impact of age and genotype. A multicentre study on 291 elderly patients

Authors :
G. Semenzato
Massimiliano Bonifacio
Mario Tiribelli
Daniela Bartoletti
Lucia Catani
Bruno Martino
Micaela Bergamaschi
Florian H. Heidel
Giuseppe A. Palumbo
Gianni Binotto
Francesca Palandri
Antonio Cuneo
Mariella D'Adda
Michele Cavo
Alessandra Iurlo
Massimo Breccia
Alessandro Isidori
Elena Sabattini
Maria Rosaria Sapienza
Nicola Polverelli
Giulia Benevolo
Roberto M. Lemoli
Nicola Sgherza
Umberto Vitolo
Monica Crugnola
Elisabetta Abruzzese
Adalberto Ibatici
Nicola Vianelli
Costanza Bosi
Franco Aversa
Roberto Latagliata
Francesco Cavazzini
Alessia Tieghi
Giovanni Martinelli
Francesca Palandri
Lucia Catani
Massimiliano Bonifacio
Giulia Benevolo
Florian Heidel
Giuseppe A. Palumbo
Monica Crugnola
Elisabetta Abruzzese
Daniela Bartoletti
Nicola Polverelli
Micaela Bergamaschi
Mario Tiribelli
Alessandra Iurlo
Massimo Breccia
Francesco Cavazzini
Alessia Tieghi
Gianni Binotto
Alessandro Isidori
Bruno Martino
Mariella D'Adda
Costanza Bosi
Elena Sabattini
Umberto Vitolo
Franco Aversa
Adalberto Ibatici
Roberto M. Lemoli
Nicola Sgherza
Antonio Cuneo
Giovanni Martinelli
Giampietro Semenzato
Michele Cavo
Nicola Vianelli
Maria R. Sapienza
Roberto Latagliata
Source :
British journal of haematology. 183(1)
Publication Year :
2018

Abstract

Ruxolitinib is a JAK1/2 inhibitor that may control myelofibrosis (MF)-related splenomegaly and symptoms and can be prescribed regardless of age. While aging is known to correlate with worse prognosis, no specific analysis is available to confirm that ruxolitinib is suitable for use in older populations. A clinical database was created in 23 European Haematology Centres and retrospective data on 291 MF patients treated with ruxolitinib when aged ≥65 years were analysed in order to assess the impact of age and molecular genotype on responses, toxicities and survival. Additional mutations were evaluated by a next generation sequencing (NGS) approach in 69 patients with available peripheral blood samples at the start of ruxolitinib treatment. Compared to older (age 65-74 years) patients, elderly (≥75 years) showed comparable responses to ruxolitinib, but higher rates of drug-induced anaemia and thrombocytopenia and worse survival. Nonetheless, the ruxolitinib discontinuation rate was comparable in the two age groups. Number and types of molecular abnormalities were comparable across age groups. However, the presence of high molecular risk (HMR) mutations significantly affected survival, counterbalancing the effect of aging. Indeed, elderly patients with

Details

ISSN :
13652141
Volume :
183
Issue :
1
Database :
OpenAIRE
Journal :
British journal of haematology
Accession number :
edsair.doi.dedup.....e5fcba8eb0dec4f4376af60ab94b819d