Enasidenib

Enasidenib is an orally available, selective, potent, small molecule inhibitor of mutant isocitrate dehydrogenase 2 (IDH2). Neomorphic mutations in IDH2 are frequently found in both hematologic malignancies and solid tumors and lead to the production of the oncometabolite (R)-2-hydroxyglutarate. Inc...

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Bibliographic Details
Main Authors: Krämer, Alwin (Author) , Bochtler, Tilmann (Author)
Format: Chapter/Article
Language:English
Published: 02 August 2018
In: Small molecules in hematology
Year: 2018, Pages: 187-197
DOI:10.1007/978-3-319-91439-8_9
Online Access:Verlag, Volltext: https://doi.org/10.1007/978-3-319-91439-8_9
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Author Notes:Alwin Krämer, Tilmann Bochtler
Description
Summary:Enasidenib is an orally available, selective, potent, small molecule inhibitor of mutant isocitrate dehydrogenase 2 (IDH2). Neomorphic mutations in IDH2 are frequently found in both hematologic malignancies and solid tumors and lead to the production of the oncometabolite (R)-2-hydroxyglutarate. Increased levels of (R)-2-hydroxyglutarate cause histone and DNA hypermethylation associated with blocked differentiation and tumorigenesis. In PDX mice transplanted with human IDH2-mutant acute myeloid leukemia cells, enasidenib treatment led to normalization of (R)-2-hydroxyglutarate serum levels, differentiation of leukemic blasts and increased survival. Early clinical data in patients with relapsed/refractory IDH2-mutant acute myeloid leukemia show that enasidenib is well tolerated and induces durable complete remissions as a single agent in about 20% of cases. One notable drug-related adverse effect is differentiation syndrome. On the basis of these results the compound has recently been approved for the treatment of relapsed/refractory IDH2-mutant acute myeloid leukemia in the USA. Although no data are available yet, clinical trials on the treatment of patients with several types of IDH2-mutant solid tumors including gliomas, chondrosarcomas and cholangiocarcinomas are currently being performed.
Item Description:Gesehen am 28.10.2019
Physical Description:Online Resource
ISBN:9783319914398
DOI:10.1007/978-3-319-91439-8_9