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• W2080961746 startingPage "275" @default.
• W2080961746 abstract "Polycythemia vera (PV) is a clonal disorder characterized by unwarranted production of red blood cells. In the majority of cases, PV is driven by oncogenic mutations that constitutively activate the JAK-STAT signal transduction pathway, such as JAK2 V617F, or exon 12 mutations or LNK mutations. Diagnosis of PV is based on the WHO criteria. Diagnosis of post-PV myelofibrosis is established according to the International Working Group for Myeloproliferative Neoplasms Research and Treatment criteria. Different clinical presentations of PV are discussed. Prognostication of PV is tailored to the most frequent complication during follow-up, namely, thrombosis. Age older than 60 years and prior history of thrombosis are the 2 main risk factors for disease stratification. Correlations are emerging between leukocytosis, JAK2(V617F) mutation, BM fibrosis, and different outcomes of PV, which need to be confirmed in prospective studies. In my practice, hydroxyurea is still the gold standard when cytoreduction is needed, even though pegylated IFN-alfa-2a and ruxolitinib might be useful in particular settings. Results of phase 1 or 2 studies concerning these latter agents should however be confirmed by the ongoing randomized phase 3 clinical trials. In this paper, I discuss the main problems encountered in daily clinical practice with PV patients regarding diagnosis, prognostication, and therapy." @default.
• W2080961746 created "2016-06-24" @default.
• W2080961746 creator A5009381933 @default.
• W2080961746 date "2012-07-12" @default.
• W2080961746 modified "2023-10-16" @default.
• W2080961746 title "How I treat polycythemia vera" @default.
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• W2080961746 doi "https://doi.org/10.1182/blood-2012-02-366054" @default.
• W2080961746 hasPubMedId "https://pubmed.ncbi.nlm.nih.gov/22611155" @default.
• W2080961746 hasPublicationYear "2012" @default.
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