Advances in targeted therapy for acute myeloid leukemia
- PMID: 32477567
- PMCID: PMC7238648
- DOI: 10.1186/s40364-020-00196-2
Advances in targeted therapy for acute myeloid leukemia
Abstract
Acute myeloid leukemia (AML) is a clonal malignancy characterized by genetic heterogeneity due to recurrent gene mutations. Treatment with cytotoxic chemotherapy has been the standard of care for more than half of a century. Although much progress has been made toward improving treatment related mortality rate in the past few decades, long term overall survival has stagnated. Exciting developments of gene mutation-targeted therapeutic agents are now changing the landscape in AML treatment. New agents offer more clinical options for patients and also confer a more promising outcome. Since Midostaurin, a FLT3 inhibitor, was first approved by US FDA in 2017 as the first gene mutation-targeted therapeutic agent, an array of new gene mutation-targeted agents are now available for AML treatment. In this review, we will summarize the recent advances in gene mutation-targeted therapies for patients with AML.
Keywords: Acute myeloid leukemia (AML); Gene mutation; Targeted therapy.
© The Author(s) 2020.
Conflict of interest statement
Competing interestsThe authors declare that they have no competing interests.
References
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- Tallman M. Prognostic significance of molecular markers and targeted regimens in the Management of Acute Myeloid Leukemia. J Natl Compr Cancer Netw. 2018;16(5S):656–659. - PubMed
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