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Blood, 15 November 2005, Vol. 106, No. 10, pp. 3377-3379.
Prepublished online as a Blood First Edition Paper on August 4, 2005; DOI 10.1182/blood-2005-05-1898.
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CLINICAL TRIALS AND OBSERVATIONS Brief report
The JAK2V617F activating mutation occurs in chronic myelomonocytic leukemia and acute myeloid leukemia, but not in acute lymphoblastic leukemia or chronic lymphocytic leukemia
Ross L. Levine,
Marc Loriaux,
Brian J. P. Huntly,
Mignon L. Loh,
Miroslav Beran,
Eric Stoffregen,
Roland Berger,
Jennifer J. Clark,
Stephanie G. Willis,
Kim T. Nguyen,
Nikki J. Flores,
Elihu Estey,
Norbert Gattermann,
Scott Armstrong,
A. Thomas Look,
James D. Griffin,
Olivier A. Bernard,
Michael C. Heinrich,
D. Gary Gilliland,
Brian Druker, and
Michael W. N. Deininger
From the Brigham and Women's Hospital, Harvard Medical School, Boston, MA; the Oregon Health and Science University (OHSU), Cancer Institute, Portland, OR; OHSU Cancer Center, Howard Hughes Medical Institute, Portland, OR; the Department of Pediatrics, University of California, San Francisco (UCSF), CA; the Department of Leukemia, University of Texas M. D. Anderson Cancer Center, Houston, TX; Mayo Medical School, Rochester MN; Institut National de la Santé et de la Recherche Médicale (INSERM) E0210, Institut Fédératif de Recherche Necker Enfants-Malades (IRNEM), Hôpital Necker, Paris, France; the Department of Hematology, Oncology, and Clinical Immunology, Heinrich-Heine-University, Düsseldorf, Germany; and the Dana-Farber Cancer Institute, Harvard Medical School, Boston, MA.
Activating mutations in tyrosine kinases have been identified in hematopoietic and nonhematopoietic malignancies. Recently, we and others identified a single recurrent somatic activating mutation (JAK2V617F) in the Janus kinase 2 (JAK2) tyrosine kinase in the myeloproliferative disorders (MPDs) polycythemia vera, essential thrombocythemia, and myeloid metaplasia with myelofibrosis. We used direct sequence analysis to determine if the JAK2V617F mutation was present in acute myeloid leukemia (AML), chronic myelomonocytic leukemia (CMML)/atypical chronic myelogenous leukemia (aCML), myelodysplastic syndrome (MDS), B-lineage acute lymphoblastic leukemia (ALL), T-cell ALL, and chronic lymphocytic leukemia (CLL). Analysis of 222 patients with AML identified JAK2V617F mutations in 4 patients with AML, 3 of whom had a preceding MPD. JAK2V617F mutations were identified in 9 (7.8%) of 116 CMML/a CML samples, and in 2 (4.2%) of 48 MDS samples. We did not identify the JAK2V617F disease allele in B-lineage ALL (n = 83), T-cell ALL (n = 93), or CLL (n = 45). These data indicate that the JAK2V617F allele is present in acute and chronic myeloid malignancies but not in lymphoid malignancies.

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