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Abemaciclib, a potent cyclin-dependent kinase 4 and 6 inhibitor, for treatment of ER-positive metastatic breast cancer.
- Source :
-
Future oncology (London, England) [Future Oncol] 2019 Oct; Vol. 15 (29), pp. 3309-3326. Date of Electronic Publication: 2019 Aug 29. - Publication Year :
- 2019
-
Abstract
- CDK 4/6 inhibitors have given patients with estrogen receptor (ER)-positive/HER2-negative (ER+/HER2рвд) advanced metastatic breast cancer important new therapeutic options. Abemaciclib is different to the other two licensed and approved CDK 4/6 inhibitors, palbociclib and ribociclib, both in dosing schedule (continuous vs intermittent) and toxicity profile (less neutropenia, more diarrhea), yet the magnitude of clinical benefit seen in first- and second-line studies is very similar. One of the key issues for clinicians is when to use these therapies. Ultimately, the biggest impact of abemaciclib could be in the adjuvant setting if the current MONARCH-E trial in high-risk node-positive patients is positive. The emerging biomarker work in the early breast cancer setting (i.e., neoMONARCH) may determine which tumors are most sensitive to abemaciclib.
- Subjects :
- Aminopyridines administration & dosage
Animals
Benzimidazoles administration & dosage
Breast Neoplasms metabolism
Breast Neoplasms pathology
Drug Evaluation
Female
Follow-Up Studies
Humans
Mice
Neoplasm Metastasis
Piperazines administration & dosage
Prognosis
Purines administration & dosage
Pyridines administration & dosage
Survival Rate
Tumor Cells, Cultured
Xenograft Model Antitumor Assays
Antineoplastic Combined Chemotherapy Protocols therapeutic use
Breast Neoplasms drug therapy
Cyclin-Dependent Kinase 4 antagonists & inhibitors
Cyclin-Dependent Kinase 6 antagonists & inhibitors
Molecular Targeted Therapy
Receptors, Estrogen metabolism
Subjects
Details
- Language :
- English
- ISSN :
- 1744-8301
- Volume :
- 15
- Issue :
- 29
- Database :
- MEDLINE
- Journal :
- Future oncology (London, England)
- Publication Type :
- Academic Journal
- Accession number :
- 31464525
- Full Text :
- https://doi.org/10.2217/fon-2019-0169