Abemaciclib: safety and effectiveness of a unique cyclin-dependent kinase inhibitor.
Aminopyridines
/ administration & dosage
Antineoplastic Combined Chemotherapy Protocols
/ administration & dosage
Aromatase Inhibitors
/ administration & dosage
Benzimidazoles
/ administration & dosage
Breast Neoplasms
/ drug therapy
Cell Cycle Checkpoints
/ drug effects
Cyclin-Dependent Kinase 4
/ antagonists & inhibitors
Cyclin-Dependent Kinase 6
/ antagonists & inhibitors
Female
Fulvestrant
/ administration & dosage
Humans
Protein Kinase Inhibitors
/ administration & dosage
Quality of Life
Abemaciclib
breast cancer
hormonal receptors
metastases
safety
Journal
Expert opinion on drug safety
ISSN: 1744-764X
Titre abrégé: Expert Opin Drug Saf
Pays: England
ID NLM: 101163027
Informations de publication
Date de publication:
Aug 2020
Aug 2020
Historique:
pubmed:
20
6
2020
medline:
28
1
2021
entrez:
20
6
2020
Statut:
ppublish
Résumé
The discovery and the clinical availability of novel cyclin-dependent kinases 4 and 6 inhibitors have profoundly changed the therapeutic scenario of metastatic hormone receptor-positive breast carcinoma. Among these inhibitors, abemaciclib can induce potent and sustained cell cycle arrest and immune system stimulation. This review summarizes the safety profile and clinical efficacy data on abemaciclib alone or in combination with aromatase inhibitors or fulvestrant in metastatic hormone receptor-positive breast carcinoma. The management of patients treated with abemaciclib is the object of this paper. As shown in phase 2 and 3 clinical trials on efficacy and tolerability, abemaciclib is a potentially convenient, safe, and effective agent for the treatment of patients with advanced hormone receptor-positive patients. Orally administered abemaciclib in combination with aromatase inhibitors or fulvestrant has the potential to allow significant improvement in survival outcomes, quality of life, response rate, and duration of response even in poor prognosis subgroups. Adequate patients' information, clinical selection, and prompt, proactive management of side effects are mandatory.
Identifiants
pubmed: 32552035
doi: 10.1080/14740338.2020.1781814
doi:
Substances chimiques
Aminopyridines
0
Aromatase Inhibitors
0
Benzimidazoles
0
Protein Kinase Inhibitors
0
Fulvestrant
22X328QOC4
abemaciclib
60UAB198HK
CDK4 protein, human
EC 2.7.11.22
CDK6 protein, human
EC 2.7.11.22
Cyclin-Dependent Kinase 4
EC 2.7.11.22
Cyclin-Dependent Kinase 6
EC 2.7.11.22
Types de publication
Journal Article
Review
Langues
eng
Sous-ensembles de citation
IM