Preclinical activity of abemaciclib alone or in combination with antimitotic and targeted therapies in breast cancer

N O'Brien, D Conklin, R Beckmann, T Luo… - Molecular cancer …, 2018 - AACR
N O'Brien, D Conklin, R Beckmann, T Luo, K Chau, J Thomas, A Mc Nulty, C Marchal…
Molecular cancer therapeutics, 2018AACR
Abstract The cyclinD: CDK4/6: Rb axis is dysregulated in a variety of human cancers.
Targeting this pathway has proven to be a successful therapeutic approach in ER+ breast
cancer. In this study, in vitro and in vivo preclinical breast cancer models were used to
investigate the expanded use of the CDK4/6 inhibitor, abemaciclib. Using a panel of 44
breast cancer cell lines, differential sensitivity to abemaciclib was observed and was seen
predominately in the luminal ER+/HER2− and ER+/HER2+ subtypes. However, a subset of …
Abstract
The cyclinD:CDK4/6:Rb axis is dysregulated in a variety of human cancers. Targeting this pathway has proven to be a successful therapeutic approach in ER+ breast cancer. In this study, in vitro and in vivo preclinical breast cancer models were used to investigate the expanded use of the CDK4/6 inhibitor, abemaciclib. Using a panel of 44 breast cancer cell lines, differential sensitivity to abemaciclib was observed and was seen predominately in the luminal ER+/HER2 and ER+/HER2+ subtypes. However, a subset of triple-negative breast cancer (TNBC) cell lines with intact Rb signaling were also found to be responsive. Equivalent levels of tumor growth inhibition were observed in ER+/HER2, ER+/HER2+ as well as biomarker selected TNBC xenografts in response to abemaciclib. In addition, abemaciclib combined with hormonal blockade and/or HER2-targeted therapy induced significantly improved antitumor activity. CDK4/6 inhibition with abemaciclib combined with antimitotic agents, both in vitro and in vivo, did not antagonize the effect of either agent. Finally, we identified a set of Rb/E2F-regulated genes that consistently track with growth inhibitory response and constitute potential pharmacodynamic biomarkers of response to abemaciclib. Taken together, these data represent a comprehensive analysis of the preclinical activity of abemaciclib, used alone or in combination, in human breast cancer models. The subtypes most likely to respond to abemaciclib-based therapies can be identified by measurement of a specific set of biomarkers associated with increased dependency on cyclinD:CDK4/6:Rb signaling. These data support the clinical development of abemaciclib as monotherapy or as a combination partner in selected ER+/HER2, HER2+/ER+, and TNBCs. Mol Cancer Ther; 17(5); 897–907. ©2018 AACR.
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