| Literature DB >> 30143968 |
Marie Robert1, Jean-Sébastien Frenel2, Emmanuelle Bourbouloux2, Dominique Berton Rigaud2, Anne Patsouris3, Paule Augereau3, Carole Gourmelon2, Mario Campone2,4.
Abstract
Deregulated cell division, resulting in aberrant cell proliferation, is one of the key hallmarks of cancer. Cyclin-dependent kinases (CDKs) play a central role in cell cycle progression in cancer, and the clinical development of the CDK4/6 inhibitors palbociclib, ribociclib, and abemaciclib has changed clinical practice in the setting of endocrine-receptor positive breast cancer. Results of pivotal phase II and III trials investigating these CDK4/6 inhibitors in patients with endocrine receptor-positive, advanced breast cancer have demonstrated a significant improvement in progression-free survival, with a safe toxicity profile. No validated biomarkers of sensitivity or resistance exist at the moment. Future development of CDK4/6 inhibitors in breast cancer should focus on the identification of predictive biomarkers, the development of drug combinations to overcome resistance, and the application of CDK4/6 inhibitors to other breast cancer subtypes.Entities:
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Year: 2018 PMID: 30143968 DOI: 10.1007/s40265-018-0972-9
Source DB: PubMed Journal: Drugs ISSN: 0012-6667 Impact factor: 9.546