In this issue of Blood, Zimmerman and colleagues demonstrate that the tyrosine kinase inhibitor (TKI) crenolanib effectively suppresses growth of leukemic cells harboring both FLT3-ITD and FLT3-TKD mutations, the latter of which are increasingly seen to emerge as resistant mutations after FMS-like tyrosine kinase 3 (FLT3) inhibitor therapy. © 2013 by The American Society of Hematology.
CITATION STYLE
Fathi, A. T. (2013, November 21). Emergence of crenolanib for FLT3-mutant AML. Blood. American Society of Hematology. https://doi.org/10.1182/blood-2013-10-528992
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