TY - JOUR
T1 - Use of acalabrutinib in patients with mantle cell lymphoma
AU - Awan, Farrukh T.
AU - Jurczak, Wojciech
N1 - Funding Information:
FT Awan has served in an advisory role for Pharmacyclics, Gilead, AbbVie and has received research funding from Pharmacyclics and Innate Pharma. W Jurczak has received grants from Acerta, Gilead, Janssen, Merck, Pfizer, Sandoz, Takeda, and TG Therapeutics. Anja Becher, PhD, of Oxford PharmaGenesis, Oxford, UK, provided medical writing support, which was in accordance with Good Publication Practice (GPP3) guidelines and funded by AstraZeneca (Wilmington, DE, USA). The authors have no other relevant affiliations or financial involvement with any organization or entity with a financial interest in or financial conflict with the subject matter or materials discussed in the manuscript apart from those disclosed. Peer reviewers on this manuscript have no relevant financial or other relationships to disclose.
Funding Information:
This work was supported by AstraZeneca (Wilmington, DE, USA).
Publisher Copyright:
© 2018, © 2018 Informa UK Limited, trading as Taylor & Francis Group.
Copyright:
Copyright 2019 Elsevier B.V., All rights reserved.
PY - 2018/6/3
Y1 - 2018/6/3
N2 - Introduction: Acalabrutinib, a selective Bruton tyrosine kinase (BTK) inhibitor, was granted accelerated approval by the FDA on 31 October 2017 for the treatment of patients with mantle cell lymphoma (MCL) who have received at least one prior therapy. Areas covered: This narrative review provides an overview of acalabrutinib, its use in clinical practice and potential future developments. Expert commentary: BTK inhibitors have demonstrated efficacy in patients with relapsed or refractory MCL. To prepare patients for therapy, all preexisting infections should be diagnosed and treated, and infection prophylaxis undertaken. Serious adverse reactions are rare with acalabrutinib; however, patients should be made aware of common adverse events such as headaches, which usually resolve within one month without medical treatment. Interaction with other drugs appears to be less of an issue with acalabrutinib than with ibrutinib; however, patients receiving acalabrutinib therapy must be advised not to take any additional medications without first consulting with their treating physician. A key unmet medical need is treatment options for patients in whom BTK inhibitors are discontinued, because of either intolerance or refractory disease. Patients not tolerating ibrutinib could be switched to acalabrutinib, which has improved selectivity and increased tolerability. First-line treatment with acalabrutinib is being investigated.
AB - Introduction: Acalabrutinib, a selective Bruton tyrosine kinase (BTK) inhibitor, was granted accelerated approval by the FDA on 31 October 2017 for the treatment of patients with mantle cell lymphoma (MCL) who have received at least one prior therapy. Areas covered: This narrative review provides an overview of acalabrutinib, its use in clinical practice and potential future developments. Expert commentary: BTK inhibitors have demonstrated efficacy in patients with relapsed or refractory MCL. To prepare patients for therapy, all preexisting infections should be diagnosed and treated, and infection prophylaxis undertaken. Serious adverse reactions are rare with acalabrutinib; however, patients should be made aware of common adverse events such as headaches, which usually resolve within one month without medical treatment. Interaction with other drugs appears to be less of an issue with acalabrutinib than with ibrutinib; however, patients receiving acalabrutinib therapy must be advised not to take any additional medications without first consulting with their treating physician. A key unmet medical need is treatment options for patients in whom BTK inhibitors are discontinued, because of either intolerance or refractory disease. Patients not tolerating ibrutinib could be switched to acalabrutinib, which has improved selectivity and increased tolerability. First-line treatment with acalabrutinib is being investigated.
KW - Acalabrutinib
KW - B-cell malignancies
KW - Bruton tyrosine kinase inhibitor
KW - adverse events
KW - efficacy
KW - mantle cell lymphoma
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U2 - 10.1080/17474086.2018.1473030
DO - 10.1080/17474086.2018.1473030
M3 - Review article
C2 - 29737219
AN - SCOPUS:85048370976
SN - 1747-4086
VL - 11
SP - 495
EP - 502
JO - Expert Review of Hematology
JF - Expert Review of Hematology
IS - 6
ER -