The role of Bruton's tyrosine kinase inhibitors in the management of mantle cell lymphoma.
Adenine
/ analogs & derivatives
Agammaglobulinaemia Tyrosine Kinase
/ antagonists & inhibitors
Antineoplastic Agents
/ therapeutic use
Benzamides
/ administration & dosage
Humans
Immunotherapy
Lymphoma, Mantle-Cell
/ drug therapy
Piperidines
/ administration & dosage
Protein Kinase Inhibitors
/ therapeutic use
Pyrazines
/ administration & dosage
Pyrazoles
/ administration & dosage
Pyrimidines
/ administration & dosage
Acalabrutinib
B-cell lymphomas
ibrutinib
mantle cell lymphoma
zanubrutinib
Journal
Journal of oncology pharmacy practice : official publication of the International Society of Oncology Pharmacy Practitioners
ISSN: 1477-092X
Titre abrégé: J Oncol Pharm Pract
Pays: England
ID NLM: 9511372
Informations de publication
Date de publication:
Jul 2020
Jul 2020
Historique:
pubmed:
14
4
2020
medline:
28
10
2020
entrez:
14
4
2020
Statut:
ppublish
Résumé
Mantle cell lymphoma is a rare subtype of B-cell non-Hodgkin's lymphomas that is generally classified as an aggressive lymphoma requiring front-line chemo-immunotherapy with stem cell rescue. Despite effective treatment, many patients relapse or are refractory to front-line therapy. In addition, these patients may also develop drug resistance requiring novel modalities for subsequent lines. Bruton's tyrosine kinase inhibitors have demonstrated a well-tolerated safety and efficacy profile across several B-cell malignancies. Ibrutinib, acalabrutinib, and zanubrutinib are FDA-approved as treatment options for patients with Mantle cell lymphoma following one prior line of therapy. Various factors should be considered which include the adverse event profile of these agents and ability to adhere to therapy. In this article, we review the role of Bruton's tyrosine kinase inhibitors for the management of Mantle cell lymphoma and review the clinical pharmacology, pharmacokinetics, safety and efficacy, and future directions.
Identifiants
pubmed: 32279595
doi: 10.1177/1078155220915956
doi:
Substances chimiques
Antineoplastic Agents
0
Benzamides
0
Piperidines
0
Protein Kinase Inhibitors
0
Pyrazines
0
Pyrazoles
0
Pyrimidines
0
ibrutinib
1X70OSD4VX
zanubrutinib
AG9MHG098Z
Agammaglobulinaemia Tyrosine Kinase
EC 2.7.10.2
acalabrutinib
I42748ELQW
Adenine
JAC85A2161
Types de publication
Journal Article
Review
Langues
eng
Sous-ensembles de citation
IM