Journal article
Enasidenib in mutant IDH2 relapsed or refractory acute myeloid leukemia
- Abstract:
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Recurrent mutations in isocitrate dehydrogenase 2 (IDH2) occur in ∼12% of patients with acute myeloid leukemia (AML). Mutated IDH2 proteins neomorphically synthesize 2-hydroxyglutarate resulting in DNA and histone hypermethylation, which leads to blocked cellular differentiation. Enasidenib (AG-221/CC-90007) is a first-in-class, oral, selective inhibitor of mutant-IDH2 enzymes. This first-in-human phase 1/2 study assessed the maximum tolerated dose (MTD), pharmacokinetic and pharmacodynamic p...
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- Publication status:
- Published
- Peer review status:
- Peer reviewed
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Access Document
- Files:
-
-
(Accepted manuscript, pdf, 158.7KB)
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- Publisher copy:
- 10.1182/blood-2017-04-779405
Authors
Bibliographic Details
- Publisher:
- American Society of Hematology Publisher's website
- Journal:
- Blood Journal website
- Volume:
- 130
- Issue:
- 6
- Pages:
- 722-731
- Publication date:
- 2017-06-06
- Acceptance date:
- 2017-05-19
- DOI:
- EISSN:
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1528-0020
- ISSN:
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0006-4971
- Pmid:
-
28588020
- Source identifiers:
-
699355
Item Description
- Language:
- English
- Pubs id:
-
pubs:699355
- UUID:
-
uuid:0d4137c0-dbff-4bfc-ad82-78cecc6ca2bb
- Local pid:
- pubs:699355
- Deposit date:
- 2019-01-31
Terms of use
- Copyright holder:
- American Society of Hematology
- Copyright date:
- 2017
- Notes:
- © 2017 by The American Society of Hematology. This is the accepted manuscript version of the article. The final version is available online from American Society of Hematology at: https://doi.org/10.1182/blood-2017-04-779405
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