articleJournal of Clinical OncologyApr 6, 2010BRONZE OA

IDH1 and IDH2 Gene Mutations Identify Novel Molecular Subsets Within De Novo Cytogenetically Normal Acute Myeloid Leukemia: A Cancer and Leukemia Group B Study

Roswell Park Comprehensive Cancer Center · University of Iowa · +10 more institutions

PubMed
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Abstract

PURPOSE To analyze the frequency and associations with prognostic markers and outcome of mutations in IDH genes encoding isocitrate dehydrogenases in adult de novo cytogenetically normal acute myeloid leukemia (CN-AML). PATIENTS AND METHODS Diagnostic bone marrow or blood samples from 358 patients were analyzed for IDH1 and IDH2 mutations by DNA polymerase chain reaction amplification/sequencing. FLT3, NPM1, CEBPA, WT1, and MLL mutational analyses and gene- and microRNA-expression profiling were performed centrally. Results IDH mutations were found in 33% of the patients. IDH1 mutations were detected in 49 patients (14%; 47 with R132). IDH2 mutations, previously unreported in AML, were detected in 69 patients…

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764
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100%
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Authors

20

Topics & keywords

Keywords
  • IDH2
  • NPM1
  • CEBPA
  • Myeloid leukemia
  • IDH1
  • Cancer research
  • Leukemia
  • Biology
UN Sustainable Development Goals
  • Good health and well-being
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