Abstract
In a series of 105 patients with polycythemia vera, we retrospectively determined whether the JAK2V617F mutation correlated with severity of disease phenotype. Higher JAK2V617F allele burden correlated with more advanced myelofibrosis, greater splenomegaly, and higher white blood cell count, but not with age, gender, hematocrit level, or frequency of phlebotomy prior to cytoreductive therapy. Although a subgroup at increased risk for thrombosis was not clearly defined, there was a suggestion that frequency of thrombosis increased as the JAK2V617F allele burden increased. The JAK2V617F allele burden did not change significantly in treated patients with serial JAK2 analyses.
| Original language | English |
|---|---|
| Pages (from-to) | 177-182 |
| Number of pages | 6 |
| Journal | Leukemia Research |
| Volume | 35 |
| Issue number | 2 |
| DOIs | |
| State | Published - Feb 2011 |
Keywords
- Adult
- Aged
- Alleles
- DNA Mutational Analysis
- Female
- Humans
- Immunosuppressive Agents/therapeutic use
- Janus Kinase 2/genetics
- Male
- Middle Aged
- Polycythemia Vera/complications
- Primary Myelofibrosis/drug therapy
- Retrospective Studies
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