Inhibiting CDK4/6 in Breast Cancer with Palbociclib, Ribociclib, and Abemaciclib: Similarities and Differences

Drugs - Tập 81 - Trang 317-331 - 2020
C. Louwrens Braal1, Elisabeth M. Jongbloed1, Saskia M. Wilting1, Ron H. J. Mathijssen1, Stijn L. W. Koolen1,2, Agnes Jager1
1Department of Medical Oncology, Erasmus University MC Cancer Institute, Rotterdam, The Netherlands
2Department of Hospital Pharmacy, Erasmus University Medical Center, Rotterdam, the Netherlands

Tóm tắt

The cyclin-dependent kinase (CDK) 4/6 inhibitors belong to a new class of drugs that interrupt proliferation of malignant cells by inhibiting progression through the cell cycle. Three such inhibitors, palbociclib, ribociclib, and abemaciclib were recently approved for breast cancer treatment in various settings and combination regimens. On the basis of their impressive efficacy, all three CDK4/6 inhibitors now play an important role in the treatment of patients with HR+, HER2− breast cancer; however, their optimal use still needs to be established. The three drugs have many similarities in both pharmacokinetics and pharmacodynamics. However, there are some differences on the basis of which the choice for a particular CDK4/6 inhibitor for an individual patient can be important. In this article, the clinical pharmacokinetic and pharmacodynamic profiles of the three CDK4/6 inhibitors are reviewed and important future directions of the clinical applicability of CDK4/6 inhibitors will be discussed.

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