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The evolving landscape in the therapy of acute myeloid leukemia
Protein & Cell ; (12): 735-746, 2013.
Article in English | WPRIM | ID: wpr-757764
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 significant 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.
Subject(s)
Full text: Available Index: WPRIM (Western Pacific) Main subject: Pathology / Leukemia, Myeloid, Acute / Therapeutic Uses / Drug Therapy / Proto-Oncogene Proteins c-pim-1 / Elafin / Histone Deacetylase Inhibitors / TOR Serine-Threonine Kinases / Antibodies, Monoclonal, Humanized / Genetics Type of study: Prognostic study Limits: Humans Language: English Journal: Protein & Cell Year: 2013 Type: Article

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Full text: Available Index: WPRIM (Western Pacific) Main subject: Pathology / Leukemia, Myeloid, Acute / Therapeutic Uses / Drug Therapy / Proto-Oncogene Proteins c-pim-1 / Elafin / Histone Deacetylase Inhibitors / TOR Serine-Threonine Kinases / Antibodies, Monoclonal, Humanized / Genetics Type of study: Prognostic study Limits: Humans Language: English Journal: Protein & Cell Year: 2013 Type: Article