Medicine

S. Goldberg, P. Fenaux, M. Craig, E. Gyan, J. Lister, J. Kassis, A. Pigneux, G. Schiller, JungAh Jung, E. Jane Leonard, H. Fingert, P. Westervelt

2014.7.5Leukemia Research Reports

DOI: 10.1016/j.lrr.2014.06.003

tlooto Summary

Results suggest modest activity in AML, supporting further research to better understand how AAK inhibition may induce leukemic cell senescence.

Abstract

Alisertib (MLN8237) is an investigational, oral, selective, Aurora A kinase (AAK) inhibitor. In this phase 2 trial, 57 patients with acute myeloid leukemia (AML) or high-grade myelodysplastic syndrome received alisertib 50 mg BID for 7 days in 21-day cycles. Responses in 6/35 AML patients (17% response rate with an additional 49% stable disease, 34% transfusion independence) included 1 complete response lasting >1 year. No responses were observed in MDS patients. Adverse events >30% included diarrhea, fatigue, nausea, febrile neutropenia, and stomatitis. Results suggest modest activity in AML, supporting further research to better understand how AAK inhibition may induce leukemic cell senescence.

Citation format

GOLDBERG, S., et al. An exploratory phase 2 study of investigational aurora a kinase inhibitor alisertib (MLN8237) in acute myelogenous leukemia and myelodysplastic syndromes. Leukemia Research Reports, 2014, 3: 58–61.