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Updated: Apr 28, 2026
![Chemical-Induced Skin Carcinogenesis Model Using Dimethylbenz[a]Anthracene and 12-O-Tetradecanoyl Phorbol-13-Acetate DMBA-TPA](/_next/image?url=https%3A%2F%2Fcloudfront.jove.com%2FCDNSource%2Fteasers%2F60445.jpg&w=3840&q=50)
Chemical-Induced Skin Carcinogenesis Model Using Dimethylbenz[a]Anthracene and 12-O-Tetradecanoyl Phorbol-13-Acetate DMBA-TPA
Published on: December 19, 2019
CDK4/6 Inhibitor-Mediated Cutaneous Toxicity in Breast Cancer
Juan M Alcantar1, Fukai L Chuang2, David D Kim2
1Hematology and Medical Oncology, University of California Los Angeles David Geffen School of Medicine, Los Angeles, USA.
Abstract:
Cyclin-dependent kinase 4 and 6 (CDK4/6) inhibitors are currently in widespread use for the treatment of both advanced metastatic and early-stage hormone receptor (HR)-positive, human epidermal growth factor receptor (HER2)- negative breast cancer. Clinical studies in the metastatic setting have demonstrated a survival benefit with the use of ribociclib. Both abemaciclib and ribociclib have shown significant improvements in invasive disease-free survival in high-risk early-stage breast cancer. Hematologic adverse events are well characterized with the three currently approved CDK4/6 inhibitors, namely palbociclib, abemaciclib, and ribociclib. Among non-hematologic toxicities, there is a paucity of information regarding cutaneous adverse events related to these three medications. In this case report, we seek to describe the incidence, time to onset, and management of CDK4/6-mediated cutaneous adverse events.
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