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Hemorrhagic events are a life-threatening complication that occur in 3–8% of patients with PV.1 A retrospective analysis assessed the association of clinical characteristics and hemorrhagic events in 267 patients with PV.1 Results from this analysis were published in Hematology by Furuya et al.1 |
Key learnings |
At a median follow-up of 4.8 years, post-diagnosis hemorrhagic events occurred in 8.6% of patients. There was a higher rate of hemorrhagic events in patients aged <60 years vs patients aged ≥60 years (16.7% vs 5.8%; p = 0.0012). |
In the univariate analysis, WBC count ≥15.0 × 109/L (p = 0.002), palpable splenomegaly (p = 0.029), and JAK2V617F allele burden ≥80% (p = 0.003) were associated with hemorrhagic events among patients aged <60 years. |
Multivariate analysis showed that JAK2V617F allele burden ≥80% in patients aged <60 years was associated with an increased risk of hemorrhagic events (HR, 9.394; 95% CI, 1.046–84.380; p = 0.046). |
Results from this analysis identify potential risk factors for hemorrhagic events in younger patients with PV. Further studies are warranted to explore if therapies that reduce JAK2V617F allele burden may reduce the incidence of hemorrhagic events. |
Abbreviations: CI, confidence interval; HR, hazard ratio; PV, polycythemia vera; WBC, white blood cell.
References
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