1. Use of cyclin-dependent kinase (CDK) 4/6 inhibitors for hormone receptor-positive, human epidermal growth factor receptor 2-negative, metastatic breast cancer: a roundtable discussion by The Breast Cancer Therapy Expert Group (BCTEG)
- Author
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Muaiad Kittaneh, Reshma Mahtani, Robert E. Coleman, Kevin Kalinsky, Jame Abraham, Mark D. Pegram, Anthony D. Elias, Charles L. Vogel, Elyse E. Lower, Frankie A. Holmes, and E. Terry Mamounas
- Subjects
0301 basic medicine ,Oncology ,Cancer Research ,medicine.medical_specialty ,Receptor, ErbB-2 ,Breast Neoplasms ,03 medical and health sciences ,0302 clinical medicine ,Breast cancer ,Cyclin-dependent kinase ,Internal medicine ,Antineoplastic Combined Chemotherapy Protocols ,Medicine ,Animals ,Humans ,Dosing ,Molecular Targeted Therapy ,Neoplasm Metastasis ,skin and connective tissue diseases ,Protein Kinase Inhibitors ,Neoplasm Staging ,biology ,business.industry ,Kinase ,Cyclin-Dependent Kinase 4 ,Cyclin-Dependent Kinase 6 ,medicine.disease ,Metastatic breast cancer ,Expert group ,030104 developmental biology ,Receptors, Estrogen ,Hormone receptor ,030220 oncology & carcinogenesis ,biology.protein ,Female ,business ,Receptors, Progesterone ,Biomarkers ,Hormone - Abstract
To provide an overview of clinical data supporting the use of cyclin-dependent kinases 4 and 6 (CDK 4/6) inhibitors in the treatment of hormone receptor-positive (HR+), human epidermal growth factor receptor 2-negative (HER2−), metastatic breast cancer (mBC), from the perspective of the practicing oncologist community. A recent roundtable discussion was convened by The Breast Cancer Therapy Expert Group (BCTEG) to review existing data on this topic and its impact on their current practice. Level 1 evidence now supports use of a CDK 4/6 inhibitor in combination with endocrine therapy for patients with HR+, HER2−, mBC. Currently, there are no biomarkers that reliably define patients who will, or will not, benefit from the addition of a CDK 4/6 inhibitor to their endocrine therapy. Additional research is needed to identify the optimal sequencing of CDK 4/6 inhibitors in relation to other therapies as well as the optimal duration of therapy; at present, evidence suggests that use in the upfront setting is better than waiting for a later line of therapy, or adding after endocrine therapy has started. Thus far, three CDK 4/6 inhibitors—palbociclib, ribociclib, and more recently, abemaciclib—have been approved for use in the setting of HR+, HER2−, mBC. The degrees to which these agents differ in terms of CDK4/6 affinity, side-effect profiles, dosing, degree of central nervous system (CNS) penetration, optimal use in combination with antiestrogen therapy, and across other subsets of breast cancer, remain an active area of investigation.
- Published
- 2018