4.5 Article Proceedings Paper

Updates in the Management of Newly Diagnosed Acute Myeloid Leukemia

Journal

JOURNAL OF THE NATIONAL COMPREHENSIVE CANCER NETWORK
Volume 19, Issue 11.5, Pages 1358-1361

Publisher

HARBORSIDE PRESS
DOI: 10.6004/jnccn.2021.5101

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For newly diagnosed AML patients, treatment strategies depend on disease subtype and genetic mutations. While most patients with TP53 mutations do not respond well to current therapies, the emergence of targeted agents like venetoclax and glasdegib provides new options for those ineligible for intensive induction regimens.
For patients with newly diagnosed acute myeloid leukemia (AML) who are candidates for intensive induction regimens, all therapies include anthracycline- and cytarabine-based backbones. Core-binding factor AML is typically treated with gemtuzumab ozogamicin and 7 + 3 chemotherapy. Patients with FLT3-mutated (ITD or TKD ) disease should have midostaurin + 7 + 3 and consolidation, and those with secondary or therapy-related AML should be considered for CPX-351. For patients ineligible for intensive induction regimens, venetoclax has changed the game and should be used in combination with hypomethylating agents or cytarabine. Glasdegib is also approved in combination with low-dose cytarabine. Patients with IDH1/2-mutated disease can be treated with ivosidenib and enasidenib, respectively. Although enasidenib has yet to secure its spot in the up-front setting, data support its use in newly diagnosed AML. An ongoing question in the field concerns how to treat patients with TP53-mutated AML, because most patients do not respond well to currently available therapies and continue to have poor overall outcomes.

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