| Literature DB >> 28351937 |
Paola Guglielmelli1,2, Annalisa Pacilli1,2, Giada Rotunno1,2, Elisa Rumi3,4, Vittorio Rosti5, Federica Delaini6, Margherita Maffioli7,8, Tiziana Fanelli1,2,9, Alessandro Pancrazzi1,2, Daniela Pietra10, Silvia Salmoiraghi6, Carmela Mannarelli1,2, Annalisa Franci1,2, Chiara Paoli1,2, Alessandro Rambaldi6,11, Francesco Passamonti7,8, Giovanni Barosi5, Tiziano Barbui12, Mario Cazzola3,4, Alessandro M Vannucchi1,2.
Abstract
The 2016 revision of the World Health Organization (WHO) classification of myeloproliferative neoplasms defines 2 stages of primary myelofibrosis (PMF): prefibrotic/early (pre-PMF) and overt fibrotic (overt PMF) phase. In this work, we studied the clinical and molecular features of patients belonging to these categories of PMF. The diagnosis of 661 PMF patients with a bone marrow biopsy at presentation was revised according to modern criteria; clinical information and annotation of somatic mutations in both driver and selected nondriver myeloid genes were available for all patients. Compared with pre-PMF, overt PMF was enriched in patients with anemia, thrombocytopenia, leukopenia, higher blast count, symptoms, large splenomegaly, and unfavorable karyotype. The different types of driver mutations were similarly distributed between the 2 categories, whereas selected mutations comprising the high mutation risk (HMR) category (any mutations in ASXL1, SRSF2, IDH1/2, EZH2) were more represented in overt PMF. More patients with overt PMF were in higher International Prognostic Scoring System risk categories at diagnosis, and the frequency increased during follow-up, suggesting greater propensity to disease progression compared with pre-PMF. Median survival was significantly shortened in overt PMF (7.2 vs 17.6 years), with triple negativity for driver mutations and presence of HMR mutations representing independent predictors of unfavorable outcome. The findings of this "real-life" study indicate that adherence to 2016 WHO criteria allows for identification of 2 distinct categories of patients with PMF where increased grades of fibrosis are associated with more pronounced disease manifestations, adverse mutation profile, and worse outcome, overall suggesting they might represent a phenotypic continuum.Entities:
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Year: 2017 PMID: 28351937 DOI: 10.1182/blood-2017-01-761999
Source DB: PubMed Journal: Blood ISSN: 0006-4971 Impact factor: 25.476