Clinical features and outcomes of JAK2 V617F-positive polycythemia vera and essential thrombocythemia according to the JAK2 V617F allele burden
mutation status is a well-known risk factor for thrombosis in patients with myeloproliferative neoplasms. However, the clinical usefulness of V617F allele burden is under investigation. We retrospectively evaluated the impact of the V617F allele burden on clinical characteristics and outcomes of V61...
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Published in | Blood research Vol. 56; no. 4; pp. 259 - 265 |
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Main Authors | , , , , , |
Format | Journal Article |
Language | English |
Published |
Korea (South)
Korean Society of Hematology; Korean Society of Blood and Marrow Transplantation; Korean Society of Pediatric Hematology-Oncology; Korean Society on Thrombosis and Hemostasis
31.12.2021
대한혈액학회 |
Subjects | |
Online Access | Get full text |
ISSN | 2287-979X 2288-0011 |
DOI | 10.5045/br.2021.2021089 |
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Summary: | mutation status is a well-known risk factor for thrombosis in patients with myeloproliferative neoplasms. However, the clinical usefulness of
V617F allele burden is under investigation.
We retrospectively evaluated the impact of the
V617F allele burden on clinical characteristics and outcomes of
V617F-positive polycythemia vera (PV) and essential thrombocythemia (ET). The
V617F allele burden was measured using sequencing.
Altogether, 127 patients with
V617F mutation (PV, N=61; ET, N=66) were included in this study.
V617F allele burdens were positively correlated with white blood cell counts, hemoglobin values, lactate dehydrogenase levels, and platelet counts. The median values of
V617F allele burden in patients with PV and ET were 58% and 30%, respectively. A
V617F allele burden of ≥30%, older age, and a higher hemoglobin level were risk factors for thrombotic events in ET. In patients with PV, older age was the only thrombotic risk factor. The 8-year probabilities of overall survival (OS) were 82.9% in all patients. A high
V617F allele burden (≥58%) was associated with poor OS in patients with PV. For the patients with ET, the difference in 8-year OS based on the
V617F allele burden was not significant.
The
V617F allele burden was correlated with hematologic parameters and clinical outcomes. Assessing the
V617F allele burden can be helpful in predicting the thrombotic risk and disease course in patients with
V617F-positive PV and ET. |
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Bibliography: | ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 23 |
ISSN: | 2287-979X 2288-0011 |
DOI: | 10.5045/br.2021.2021089 |