A pharmacogenomic approach validates AG-221 as an effective and on-target therapy in IDH2 mutant AML

Leukemia. 2017 Jun;31(6):1466-1470. doi: 10.1038/leu.2017.84. Epub 2017 Mar 10.
No abstract available

Publication types

  • Research Support, Non-U.S. Gov't
  • Validation Study

MeSH terms

  • Aminopyridines / pharmacology
  • Aminopyridines / therapeutic use*
  • Antineoplastic Agents / pharmacology
  • Antineoplastic Agents / therapeutic use*
  • Enzyme Inhibitors / pharmacology
  • Enzyme Inhibitors / therapeutic use*
  • Humans
  • Isocitrate Dehydrogenase / antagonists & inhibitors*
  • Isocitrate Dehydrogenase / genetics
  • Leukemia, Myeloid, Acute / drug therapy*
  • Leukemia, Myeloid, Acute / enzymology
  • Leukemia, Myeloid, Acute / pathology
  • Mutation*
  • Pharmacogenetics*
  • Triazines / pharmacology
  • Triazines / therapeutic use*

Substances

  • Aminopyridines
  • Antineoplastic Agents
  • Enzyme Inhibitors
  • Triazines
  • enasidenib
  • IDH2 protein, human
  • Isocitrate Dehydrogenase