Journal article
Substantial susceptibility of chronic lymphocytic leukemia to BCL2 inhibition: Results of a phase I study of navitoclax in patients with relapsed or refractory disease
AW Roberts, JF Seymour, JR Brown, WG Wierda, TJ Kipps, SL Khaw, DA Carney, SZ He, DCS Huang, H Xiong, Y Cui, TA Busman, EM McKeegan, AP Krivoshik, SH Enschede, R Humerickhouse
Journal of Clinical Oncology | Published : 2012
Abstract
Purpose: BCL2 overexpression is a hallmark of chronic lymphocytic leukemia (CLL). The novel BH3 mimetic navitoclax (ABT-263) specifically inhibits BCL2 and related proteins BCL-xL and BCL-w, potently inducing apoptosis of CLL cells in vitro. A phase I trial in patients with CLL was conducted to evaluate the safety, pharmacokinetics, and biologic activity of oral navitoclax. Patients and Methods: Twenty-nine patients with relapsed or refractory CLL received daily navitoclax for 14 days (10, 110, 200, or 250 mg/d; n = 15) or 21 days (125, 200, 250, or 300 mg/d; n = 14) of each 21-day cycle. Dose escalation decisions were informed by continual reassessment methodology. Results: Lymphocytosis wa..
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Awarded by National Cancer Institute
Funding Acknowledgements
Research Funding: Andrew W. Roberts, Abbott Laboratories; Jennifer R. Brown, Celgene, Genzyme; William G. Wierda, GlaxoSmithKline, Abbott Laboratories; Thomas J. Kipps, Abbott LaboratoriesSupported by Abbott Laboratories and Genentech. Additional support for correlative studies was provided by National Health and Medical Research Council of Australia, Victorian Cancer Agency, Leukaemia Foundation Australia, Australian Cancer Research Foundation, and the Leukemia and Lymphoma Society.