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Protein & Cell

ISSN 1674-800X

ISSN 1674-8018(Online)

CN 11-5886/Q

Postal Subscription Code 80-984

2018 Impact Factor: 7.575

Prot Cell    2013, Vol. 4 Issue (10) : 735-746    https://doi.org/10.1007/s13238-013-3057-2      PMID: 23982740
REVIEW
The evolving landscape in the therapy of acute myeloid leukemia
Grace L. Peloquin, Yi-Bin Chen, Amir T. Fathi()
Massachusetts General Hospital Cancer Center, Harvard Medical School, Boston, MA 02114, USA
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Abstract

Acute myeloid leukemia (AML) is a heterogeneous clonal disorder of myeloid precursors arrested in their maturation, creating a diverse disease entity with a wide range of responses to historically standard treatment approaches. While signifi cant progress has been made in characterizing and individualizing the disease at diagnosis to optimally inform those affected, progress in treatment to reduce relapse and induce remission has been limited thus far. In addition to a brief summary of the factors that shape prognostication at diagnosis, this review attempts to expand on the current therapies under investigation that have shown promise in treating AML, including hypomethylating agents, gemtuzumab ozogamicin, FLT3 tyrosine kinase inhibitors, antisense oligonucleotides, and other novel therapies, including aurora kinases, mTOR and PI3 kinase inhibitors, PIM kinase inhibitors, HDAC inhibitors, and IDH targeted therapies. With these, and undoubtedly many others in the future, it is the hope that by combining more accurate prognostication with more effective therapies, patients will begin to have a different, and more complete, outlook on their disease that allows for safer and more successful treatment strategies.

Keywords acute myeloid leukemia      hypomethylating      FLT3      gemtuzumab ozogamicin     
Corresponding Author(s): Fathi Amir T.,Email:afathi@partners.org   
Issue Date: 01 October 2013
 Cite this article:   
Grace L. Peloquin,Yi-Bin Chen,Amir T. Fathi. The evolving landscape in the therapy of acute myeloid leukemia[J]. Prot Cell, 2013, 4(10): 735-746.
 URL:  
https://academic.hep.com.cn/pac/EN/10.1007/s13238-013-3057-2
https://academic.hep.com.cn/pac/EN/Y2013/V4/I10/735
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[1] Yan Jiang,Yanping Zhu,Zhi-Jie Liu,Songying Ouyang. The emerging roles of the DDX41 protein in immunity and diseases[J]. Protein Cell, 2017, 8(2): 83-89.
[2] Perry M. Chan. Differential signaling of Flt3 activating mutations in acute myeloid leukemia: a working model[J]. Prot Cell, 2011, 2(2): 108-115.
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