
doi: 10.2217/fon.15.342
pmid: 26759179
Mantle cell lymphoma (MCL) is a rare and aggressive form of non-Hodgkin lymphoma. Ibrutinib is a first-in-class, oral inhibitor of Bruton's tyrosine kinase which acts by downstream inhibition of the B-cell receptor. Early clinical trials have demonstrated excellent tolerability and a modest side-effect profile in relapsed/refractory MCL. Although the majority of disease responses are partial, efficacy data are impressive with more than two-thirds of patients demonstrating a durable response. This article focuses on all aspects of ibrutinib in the context of MCL, including a summary of the basic pharmacology and pharmacokinetics; a review of the safety and efficacy data published to date and a discussion of the future implications in MCL.
Clinical Trials as Topic, Adenine, Drug Evaluation, Preclinical, Receptors, Antigen, B-Cell, Antineoplastic Agents, Lymphoma, Mantle-Cell, Protein-Tyrosine Kinases, Pyrimidines, Treatment Outcome, Piperidines, Drug Resistance, Neoplasm, Recurrence, Antineoplastic Combined Chemotherapy Protocols, Agammaglobulinaemia Tyrosine Kinase, Animals, Humans, Pyrazoles, Protein Kinase Inhibitors
Clinical Trials as Topic, Adenine, Drug Evaluation, Preclinical, Receptors, Antigen, B-Cell, Antineoplastic Agents, Lymphoma, Mantle-Cell, Protein-Tyrosine Kinases, Pyrimidines, Treatment Outcome, Piperidines, Drug Resistance, Neoplasm, Recurrence, Antineoplastic Combined Chemotherapy Protocols, Agammaglobulinaemia Tyrosine Kinase, Animals, Humans, Pyrazoles, Protein Kinase Inhibitors
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