Acute myeloid leukemia with IDH1 and IDH2 mutations: 2021 treatment algorithm

• Published in: Blood cancer journal (New York) Vol. 11; no. 6; pp. 107 - 7
• Main Authors: Issa, Ghayas C., DiNardo, Courtney D.
• Format: Journal Article
• Language: English
• Published: London Nature Publishing Group UK 03.06.2021; Springer Nature B.V; Nature Publishing Group
• Subjects: 45/23; 631/208/68; 692/308/153; 692/699/67/1059; Algorithms; Biomedical and Life Sciences; Biomedicine; Blood cancer; Cancer Research; Chemotherapy; Current Treatment Algorithm; Hematology; Humans; Isocitrate Dehydrogenase - genetics; Leukemia; Leukemia, Myeloid, Acute - enzymology; Leukemia, Myeloid, Acute - genetics; Leukemia, Myeloid, Acute - therapy; Mutation; Neoplasm Proteins - genetics; Oncology
• ISSN: 2044-5385; 2044-5385
• DOI: 10.1038/s41408-021-00497-1

Acute myeloid leukemia is a genetically heterogeneous hematologic malignancy; approximately 20% of AML harbors a mutation in the isocitrate dehydrogenase ( IDH ) genes, IDH1 or IDH2 . These recurrent mutations in key metabolic enzymes lead to the production of the oncometabolite 2-hydroxyglutarate, which promotes leukemogenesis through a block in normal myeloid differentiation. Since this discovery, selective oral inhibitors of mutant IDH1 and IDH2 have subsequently been developed and are now approved as single agent therapy, based on clinical efficacy observed within the original first-in-human trials. The investigation of IDH inhibitors in combination with standard therapies such as azacytidine, with intensive chemotherapy, and with other small molecule targeted therapies in rational combinations are currently under evaluation to further improve upon clinical efficacy.