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induces a good molecular response in a patient with chronic eosinophilic leukemia (CEL) carrying the JAK2V617F point mutation
1 Departament of Haematology and Bone Marrow Transplantation, Silesian Medical University, Katowice, Poland;
2 Institute of Hematology and Transfusion Medicine, Warsaw, Poland
Correspondence: Grzegorz Helbig, MD. Departament of Haematology and Bone Marrow Transplantation, Silesian Medical University, 40-027 Katowice, Dabrowski str. 25, Poland Tel: +48.322591236, Fax: +48.322554985. E-mail: ghelbig{at}o2.pl
The JAK2 V617F point mutation is very rare in hypereosinophilic syndome and/or chronic eosinophilic leukemia. Here we report on a patient with chronic eosinophilic leukemia and detectable JAK2 mutant clone, who achieved a good molecular response to interferon
-2a after 4 months of treatment. The molecular response correlated with only moderate haematological improvement
Key words: JAK2 V617F mutation, interferon
, hypereosinophilic syndrome, chronic eosinophilic leukemia, molecular response.
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