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Core‐binding factor acute myeloid leukemia: Heterogeneity, monitoring, and therapy
Author(s) -
Solh Melhem,
Yohe Sophia,
Weisdorf Daniel,
Ustun Celalettin
Publication year - 2014
Publication title -
american journal of hematology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.456
H-Index - 105
eISSN - 1096-8652
pISSN - 0361-8609
DOI - 10.1002/ajh.23821
Subject(s) - core binding factor , myeloid leukemia , medicine , leukemia , oncology , minimal residual disease , disease , myeloid , biology , gene , genetics , transcription factor
Core binding factor acute myelogenous leukemia (CBF AML) constitutes 15% of adult AML and carries an overall good prognosis. CBF AML encodes two recurrent cytogentic abnormalities referred to as t(8;21) and inv (16). The two CBF AML entities are usually grouped together but there is a considerable clinical, pathologic and molecular heterogeneity within this group of diseases. Recent and ongoing studies are addressing the molecular heterogeneity, minimal residual disease and targeted therapies to improve the outcome of CBF AML. In this article, we present a comprehensive review about CBF AML with emphasis on molecular heterogeneity and new therapeutic options. Am. J. Hematol. 89:1121–1131, 2014. © 2014 Wiley Periodicals, Inc.

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