IDH1 and IDH2 mutations are frequent genetic alterations in acute myeloid leukemia and confer adverse prognosis in cytogenetically normal acute myeloid leukemia with NPM1 mutation without FLT3 internal tandem duplication.

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Summary

IDH1 and IDH2 mutations are recurring genetic changes in AML that constitute a poor prognostic factor in CN-AML with mutated NPM1 without FLT3-ITD, which allows refined risk stratification of this AML subset.

Type
article
Published
2010-08-01
Cited by
811
References
45

Keywords

NPM1, IDH2, CEBPA, Myeloid leukemia, Medicine

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