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Clinical and molecular response of AML harboring non-canonical <i>FLT3</i> N676K driver mutations to contemporary FLT3 inhibitors

2022-09-19

Abstract excerpt

<h4>ABSTRACT</h4> The treatment of acute myeloid leukemia (AML) has been enhanced by the development and regulatory approval of a series of novel agents, including midostaurin and gilteritinib (FLT3 inhibitors), venetoclax (BCL2 inhibitor), ivosidenib (IDH1 inhibitor), and enasidenib (IDH2 inhibitor). A difficulty that has arisen in the era of molecular therapies, however, is determining the efficacy of these agen...

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Literature Corpus work
4b03ccca-2585-525b-995b-002c3571854f
DOI
10.1101/2022.09.15.22279953
Open publication

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Clinical and molecular response of AML harboring non-canonical <i>FLT3</i> N676K driver mutations to contemporary FLT3 inhibitorsDOI 10.1101/2022.09.15.22279953
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