Journal article
Venetoclax in patients with previously treated chronic lymphocytic leukemia
AW Roberts, S Stilgenbauer, JF Seymour, DCS Huang
Clinical Cancer Research | AMER ASSOC CANCER RESEARCH | Published : 2017
Abstract
Venetoclax is the first BCL2 inhibitor to enter routine clinical practice. It is an orally bioavailable small molecule that binds BCL2 very specifically. Acting as a pharmacologic mimic of the proteins that initiate apoptosis (a so-called BH3 mimetic), venetoclax rapidly induces apoptosis in chronic lymphocytic leukemia (CLL) cells, which express high levels of BCL2 and rely on it to maintain their survival. As a single agent, daily venetoclax treatment induced durable responses in 79% of patients with relapsed or refractory CLL or small lymphocytic lymphoma in a phase I study, including complete remissions in 20% of patients. Its use was approved by the FDA in April 2016 for patients with p..
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Awarded by Roche
Funding Acknowledgements
Research by A.W. Roberts and D.C.S. Huang is supported by fellowships and grants from the National Health and Medical Research Council of Australia (1079560, 1043149), the Leukemia & Lymphoma Society (7001-13), the Victorian Cancer Agency (TRP13041), and the Australian Cancer Research Foundation. S. Stilgenbauer received support from EC TransCan program (FIRE CLL), DFG (SFB1074 subproject B1), and BMBF (PReCISE).