TY - JOUR
T1 - Acute myeloid leukemia
T2 - current progress and future directions
AU - Kantarjian, Hagop
AU - Kadia, Tapan
AU - DiNardo, Courtney
AU - Daver, Naval
AU - Borthakur, Gautam
AU - Jabbour, Elias
AU - Garcia-Manero, Guillermo
AU - Konopleva, Marina
AU - Ravandi, Farhad
N1 - Publisher Copyright:
© 2021, The Author(s).
PY - 2021/2
Y1 - 2021/2
N2 - Progress in the understanding of the biology and therapy of acute myeloid leukemia (AML) is occurring rapidly. Since 2017, nine agents have been approved for various indications in AML. These included several targeted therapies like venetoclax, FLT3 inhibitors, IDH inhibitors, and others. The management of AML is complicated, highlighting the need for expertise in order to deliver optimal therapy and achieve optimal outcomes. The multiple subentities in AML require very different therapies. In this review, we summarize the important pathophysiologies driving AML, review current therapies in standard practice, and address present and future research directions.
AB - Progress in the understanding of the biology and therapy of acute myeloid leukemia (AML) is occurring rapidly. Since 2017, nine agents have been approved for various indications in AML. These included several targeted therapies like venetoclax, FLT3 inhibitors, IDH inhibitors, and others. The management of AML is complicated, highlighting the need for expertise in order to deliver optimal therapy and achieve optimal outcomes. The multiple subentities in AML require very different therapies. In this review, we summarize the important pathophysiologies driving AML, review current therapies in standard practice, and address present and future research directions.
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U2 - 10.1038/s41408-021-00425-3
DO - 10.1038/s41408-021-00425-3
M3 - Review article
C2 - 33619261
AN - SCOPUS:85101404837
SN - 2044-5385
VL - 11
JO - Blood cancer journal
JF - Blood cancer journal
IS - 2
M1 - 41
ER -