Erschienen in:
26.07.2019 | Molecular Testing and Diagnostics (J Khoury, Section Editor)
Acute Myeloid Leukemia: from Mutation Profiling to Treatment Decisions
verfasst von:
Courtney DiNardo, Curtis Lachowiez
Erschienen in:
Current Hematologic Malignancy Reports
|
Ausgabe 5/2019
Einloggen, um Zugang zu erhalten
Abstract
Purpose of Review
Awareness of the molecular landscape of AML has improved AML care over the last 5 years. This review summarizes updates regarding the diagnostic and therapeutic relevance of key mutations in AML.
Recent Findings
Molecular mutations in genes including NPM1, CEBPA, FLT3, IDH1/2, TP53, RUNX1, and ASXL1 provide important prognostic and/or therapeutic information in AML, including best treatment strategies, transplant recommendations, and significance of MRD detection. Mutational analysis has led to the recognition of new entities including hereditary leukemia syndromes and clonal hematopoiesis of indeterminate potential (CHIP). FLT3 and IDH1/2 mutations are the focus of targeted therapies in the treatment of AML.
Summary
Advances in the molecular characterization of AML have provided an improved understanding of leukemogenesis and AML risk stratification, improved disease monitoring techniques, optimized therapeutic strategies, and have led to the development of novel molecular-targeted therapeutics. Ongoing genomic advances will continue to improve upon the outcome of patients with AML.