Abstract |
We report a 55 year old woman with post-ET PV for 12 years, who experienced resolution of severe constitutional symptoms within 3 days, a marked reduction in splenomegaly and a rapid decline in the JAK2V617F allele burden during combination therapy with interferon-alpha2a and ruxolitinib. Within 4 weeks the patient achieved complete hematological remission with normalization of peripheral blood counts and within 10 months the JAK2V617F-allele burden was reduced from 90% to 28%. Such a rapid decline in the JAK2V617F allele burden is highly unusual in PV-patients during low-dose IFN-alpha2 monotherapy and this finding warrants a prospective study with combination therapy.
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Authors | M E Bjørn, K de Stricker, L Kjær, K Ellemann, H C Hasselbalch |
Journal | Leukemia research reports
(Leuk Res Rep)
Vol. 3
Issue 2
Pg. 73-5
( 2014)
ISSN: 2213-0489 [Print] England |
PMID | 25379406
(Publication Type: Journal Article)
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