Background:
Acute myeloid leukemia is the collective name for different types of leukemias of
myeloid origin affecting blood and bone marrow. The overproduction of immature myeloblasts (white blood
cells) is the characteristic feature of AML, thus flooding the bone marrow and reducing its capacity to produce
normal blood cells. USFDA on August 1, 2017, approved a drug named Enasidenib formerly known as AG-221
which is being marketed under the name Idhifa to treat R/R AML with IDH2 mutation. The present review
depicts the broad profile of enasidenib including various aspects of chemistry, preclinical, clinical studies,
pharmacokinetics, mode of action and toxicity studies.
Methods:
Various reports and research articles have been referred to summarize different aspects related to
chemistry and pharmacokinetics of enasidenib. Clinical data was collected from various recently published
clinical reports including clinical trial outcomes.
Result:
The various findings of enasidenib revealed that it has been designed to allosterically inhibit mutated
IDH2 to treat R/R AML patients. It has also presented good safety and efficacy profile along with 9.3 months
overall survival rates of patients in which disease has relapsed. The drug is still under study either in combination
or solely to treat hematological malignancies. Molecular modeling studies revealed that enasidenib binds to
its target through hydrophobic interaction and hydrogen bonding inside the binding pocket. Enasidenib is found
to be associated with certain adverse effects like elevated bilirubin level, diarrhea, differentiation syndrome,
decreased potassium and calcium levels, etc.
Conclusion:
Enasidenib or AG-221was introduced by FDA as an anticancer agent which was developed as a
first in class, a selective allosteric inhibitor of the tumor target i.e. IDH2 for Relapsed or Refractory AML. Phase
1/2 clinical trial of Enasidenib resulted in the overall survival rate of 40.3% with CR of 19.3%. Phase III trial on
the Enasidenib is still under process along with another trial to test its potency against other cell lines.
Edasidenib is associated with certain adverse effects, which can be reduced by investigators by designing its
newer derivatives on the basis of SAR studies. Hence, it may come in the light as a potent lead entity for anticancer
treatment in the coming years.
Combinatorial targeting of XPO1 and FLT3 exerts synergistic anti-leukemia effects through induction of differentiation and apoptosis in FLT3-mutated acute myeloid leukemias: from concept to clinical trial
