Preclinical and clinical development of palbociclib and future perspectives.
E Martínez de DueñasJ Gavila-GregoriS Olmos-AntónA Santaballa-BertránA Lluch-HernándezE J Espinal-DomínguezM Rivero-SilvaA Llombart-CussacPublished in: Clinical & translational oncology : official publication of the Federation of Spanish Oncology Societies and of the National Cancer Institute of Mexico (2018)
Cyclin-dependent kinases (CDKs) play a key role in cell cycle regulation, which makes them a clear therapeutic target to interfere with cell division and proliferation in cancer patients. Palbociclib, a specific inhibitor of CDK4/6 with outstanding clinical efficacy data and limited toxicity, has been recently approved for the treatment of hormone receptor (HR)-positive human epidermal growth factor receptor 2 (HER2)-negative locally advanced or metastatic breast cancer, either in combination with an aromatase inhibitor or in combination with fulvestrant in women who have received prior endocrine therapy. This review describes the mechanism of action, preclinical experiences and clinical data of palbociclib, with a special focus on integrating this data with the positioning of palbociclib in the current clinical guidelines for advanced HR-positive/HER2-negative breast cancer. Aspects of the ongoing major studies are also presented, as well as future prospects in the development of palbociclib.
Keyphrases
- metastatic breast cancer
- cell cycle
- epidermal growth factor receptor
- electronic health record
- cell proliferation
- cell therapy
- locally advanced
- squamous cell carcinoma
- endothelial cells
- signaling pathway
- current status
- type diabetes
- adipose tissue
- bone marrow
- insulin resistance
- machine learning
- pregnant women
- lymph node
- polycystic ovary syndrome
- radiation therapy
- mesenchymal stem cells
- deep learning
- pi k akt