Mechanisms of resistance to targeted therapies for relapsed or refractory acute myeloid leukemia
被引:8
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作者:
Kropp, Erin M.
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Univ Michigan Ann Arbor, Dept Internal Med, Ann Arbor, MI USAUniv Michigan Ann Arbor, Dept Internal Med, Ann Arbor, MI USA
Kropp, Erin M.
[1
]
Li, Qing
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Univ Michigan Ann Arbor, Dept Internal Med, Ann Arbor, MI USA
Univ Michigan Ann Arbor, 109 Zina Pitcher Pl,BSRB1520, Ann Arbor, MI 48109 USAUniv Michigan Ann Arbor, Dept Internal Med, Ann Arbor, MI USA
Li, Qing
[1
,2
]
机构:
[1] Univ Michigan Ann Arbor, Dept Internal Med, Ann Arbor, MI USA
[2] Univ Michigan Ann Arbor, 109 Zina Pitcher Pl,BSRB1520, Ann Arbor, MI 48109 USA
Acute myeloid leukemia (AML) is an aggressive disease of clonal hematopoiesis with a high rate of relapse and refractory disease despite intensive therapy. Traditionally, relapsed or refractory AML has increased therapeutic resistance and poor long-term survival. In recent years, advancements in the mechanistic understanding of leukemogenesis have allowed for the development of targeted therapies. These therapies offer novel alternatives to intensive chemotherapy and have prolonged survival in relapsed or refractory AML. Unfortunately, a significant portion of patients do not respond to these therapies and relapse occurs in most patients who initially responded. This review focuses on the mechanisms of resistance to targeted therapies in relapsed or refractory AML.(c) 2022 ISEH - Society for Hematology and Stem Cells. Published by Elsevier Inc. All rights reserved.
机构:
Mem Sloan Kettering Canc Ctr, Leukemia Serv, 1275 York Ave, New York, NY 10065 USAMem Sloan Kettering Canc Ctr, Leukemia Serv, 1275 York Ave, New York, NY 10065 USA