Thromboses and hemorrhages are common in MPN patients with high JAK2V617F allele burden
Autor: | Fabrizio Fabris, Irene Bertozzi, Anna Maria Lombardi, Giulia Bogoni, Elena Duner, Giacomo Biagetti, Maria Luigia Randi |
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Rok vydání: | 2017 |
Předmět: |
Male
Kaplan-Meier Estimate Gastroenterology Myeloproliferative neoplasms Essential 0302 clinical medicine Polycythemia vera Gene Frequency Risk Factors 80 and over Thrombocythemia Polycythemia Vera Aged 80 and over Hemorrhage JAK2V617F allele burden Thrombosis Adult Aged Alleles Female Humans Janus Kinase 2 Middle Aged Multivariate Analysis Myeloproliferative Disorders Primary Myelofibrosis Proportional Hazards Models Risk Assessment Thrombocythemia Essential Mutation Missense Hematology Incidence (epidemiology) General Medicine Quartile 030220 oncology & carcinogenesis medicine.medical_specialty 03 medical and health sciences Internal medicine medicine Allele Myelofibrosis Allele frequency Essential thrombocythemia business.industry Proportional hazards model medicine.disease Surgery Mutation Missense business 030215 immunology |
Zdroj: | Annals of Hematology. 96:1297-1302 |
ISSN: | 1432-0584 0939-5555 |
DOI: | 10.1007/s00277-017-3040-8 |
Popis: | The most common causes of morbidity and mortality in myeloproliferative neoplasms (MPN) are thrombotic and hemorrhagic complications. The JAK2V617F mutation, commonly found in MPN, correlates with several clinical and laboratory characteristics even if the relevance of JAK2V617F allele burden in the natural history of these diseases is unclear. In this study we searched, a relation between thrombotic and hemorrhagic complications and JAK2V617F allele burden level in MPN patients. We evaluated 253 consecutive MPN [121 essential thrombocythemia (ET), 124 polycythemia vera (PV), and 8 primary myelofibrosis (PMF)] patients in whom the JAK2V617F allele burden was available, all studied and followed (median 8.8 years) in our department. Patients were stratified accordingly to their JAK2V617F allele burden, into four quartiles (1st25%, 2nd 26-50%, 3rd 51-75%, and 4th75%). Significantly higher incidence of thromboses (p = 0.001) and hemorrhages (p 0.001) during follow-up has been observed in higher quartiles when compared to lower ones. Thrombosis- and hemorrhage-free survivals were poorer in patients belonging to the highest quartile. Our data suggest that MPN patients with JAK2V617F allele burden higher than 75% have to be considered as high risk patients, being prone to develop thrombo-hemorrhagic complications during the disease course. |
Databáze: | OpenAIRE |
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