CDK4/6 Inhibition as a therapeutic strategy in breast cancer: palbociclib, ribociclib, and abemaciclib.

Bahar Laderian, Tito Fojo

Journal: Seminars in oncology 2019;44(6):395-403

PMID: 29935901

Abstract

With 40,920 American women expected to die from breast cancer in 2018 and global health estimates that more than 508,000 women died in 2011 from this disease, the identification of novel therapeutic strategies for the treatment of breast cancer cannot be ignored. A breakthrough class of cancer drugs that has emerged in recent years and has had an impact in the treatment of breast cancer are the cyclin-dependent kinase 4 and 6 (CDK4/6) inhibitors, with palbociclib the first in class to have received regulatory approval for breast cancer. In this article we will compare and contrast three CDK4/6 inhibitors - palbociclib, ribociclib and abemaciclib - that have received regulatory approval for the treatment of metastatic breast cancer. Ribociclib and abemaciclib developed after the success of palbociclib represent examples of "me-too" therapies increasingly being deployed in oncology.

Copyright © 2017. Published by Elsevier Inc.

Address: Division of Hematology Oncology, Department of Medicine, Columbia University Medical Center, New York, NY.; Division of Hematology Oncology, Department of Medicine, Columbia University Medical Center, New York, NY; James J. Peters VAMC, Bronx, NY. Electronic address: [email protected].
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