Acalabrutinib for adults with mantle cell lymphoma.
Adenine
/ analogs & derivatives
Adult
Agammaglobulinaemia Tyrosine Kinase
/ antagonists & inhibitors
Animals
Antineoplastic Agents
/ administration & dosage
Benzamides
/ administration & dosage
Humans
Lymphoma, Mantle-Cell
/ drug therapy
Piperidines
Protein Kinase Inhibitors
/ administration & dosage
Pyrazines
/ administration & dosage
Pyrazoles
/ administration & dosage
Pyrimidines
/ administration & dosage
Survival Rate
Acalabrutinib
Bruton tyrosine kinase inhibitors
adverse events
mantle cell lymphoma
Journal
Expert review of clinical pharmacology
ISSN: 1751-2441
Titre abrégé: Expert Rev Clin Pharmacol
Pays: England
ID NLM: 101278296
Informations de publication
Date de publication:
Mar 2019
Mar 2019
Historique:
pubmed:
15
1
2019
medline:
28
2
2019
entrez:
15
1
2019
Statut:
ppublish
Résumé
Although advances in mantle cell lymphoma (MCL) therapy have improved overall survival (OS), managing relapsed/refractory (R/R) cases remains a great challenge. Bruton tyrosine kinase (BTK) inhibitors have broadened therapeutic options in MCL and became the backbone of second-line strategies. Areas covered: Ibrutinib, the first-in-class BTK inhibitor registered for MCL therapy, is efficient, with clear benefits of its use. However, ibrutinib-related adverse events due to off-target inhibition of other kinases led to the development of more selective molecules with comparable efficacy and better safety profiles. Expert commentary: Acalabrutinib, a new BTK inhibitor, currently being evaluated in numerous clinical studies is approved by FDA in relapsing/refractory MCL. Its role will evolve over the next few years. Efficacy and good tolerability of acalabrutinib gives even greater opportunity for potential upfront use and new therapeutic combinations, including monoclonal antibodies, antibody-drug conjugates, immune checkpoint inhibitors, bcl-2 (B-cell lymphoma-2) or IP3K (phosphoinositide 3-kinase) inhibitors.
Identifiants
pubmed: 30638402
doi: 10.1080/17512433.2019.1568868
doi:
Substances chimiques
Antineoplastic Agents
0
Benzamides
0
Piperidines
0
Protein Kinase Inhibitors
0
Pyrazines
0
Pyrazoles
0
Pyrimidines
0
ibrutinib
1X70OSD4VX
Agammaglobulinaemia Tyrosine Kinase
EC 2.7.10.2
BTK protein, human
EC 2.7.10.2
acalabrutinib
I42748ELQW
Adenine
JAC85A2161
Types de publication
Journal Article
Review
Langues
eng
Sous-ensembles de citation
IM