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Enasidenib: An Oral IDH2 Inhibitor for the Treatment of Acute Myeloid Leukemia.
Myers, Rebecca A; Wirth, Scott; Williams, Sherry; Kiel, Patrick J.
Afiliación
  • Myers RA; Indiana University Simon Cancer Center-IU Health, Indianapolis, Indiana.
  • Wirth S; University of Illinois at Chicago Cancer Center and University of Illinois at Chicago College of Pharmacy, Chicago, Illinois.
  • Williams S; Department of Pharmacy, The James Cancer Hospital and Solove Research Institute, Columbus, Ohio.
  • Kiel PJ; Indiana University School of Medicine, Indianapolis, Indiana.
J Adv Pract Oncol ; 9(4): 435-440, 2018.
Article en En | MEDLINE | ID: mdl-30719396
ABSTRACT
Acute myeloid leukemia (AML) is a hematologic malignancy that affects predominantly older patients, with a median age of diagnosis around 67. Overall prognosis is poor; however, novel targeted therapies that can potentially improve outcomes in these patients have emerged in recent years. Mutations in isocitrate dehydrogenase (IDH) occur in 20% of AML diagnoses. IDH2 performs a crucial role in cellular metabolism, and when this enzyme is inhibited, the cell cannot rid itself of endogenous products and is thus marked for apoptosis. The US Food and Drug Administration (FDA) approved the first mutant IDH2 inhibitor, enasidenib, for patients with relapsed or refractory IDH2-mutated AML detected by an FDA-approved test.

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Idioma: En Revista: J Adv Pract Oncol Año: 2018 Tipo del documento: Article

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Idioma: En Revista: J Adv Pract Oncol Año: 2018 Tipo del documento: Article