Review of Bruton tyrosine kinase inhibitors for the treatment of relapsed or refractory mantle cell lymphoma

  • C. Owen University of Calgary and Foothills Medical Centre
  • N. L. Berinstein University of Toronto and Odette Cancer Centre, Sunnybrook Health Sciences Centre
  • A. Christofides Impact Medicom Inc
  • L. H. Sehn Centre for Lymphoid Cancer, University of British Columbia,
Keywords: Bruton tyrosine kinase inhibitors, mantle cell lymphoma, acalabrutinib

Abstract

Mantle cell lymphoma (mcl) is a rare subtype of aggressive B-cell non-Hodgkin lymphoma that remains incurable with standard therapy. Patients typically require multiple lines of therapy, and those with relapsed or refractory (r/r) disease have a very poor prognosis. The Bruton tyrosine kinase (btk) inhibitor ibrutinib has proven to be an effective agent for patients with r/r mcl. Although usually well tolerated, ibrutinib can be associated with unique toxicities, requiring discontinuation in some patients. Effective and well-tolerated alternatives to ibrutinib for patients with r/r mcl are therefore needed. Novel btk inhibitors such as acalabrutinib, zanubrutinib, and tirabrutinib are designed to improve on the safety and efficacy of first-generation btk inhibitors such as ibrutinib. Data from single-arm clinical trials suggest that, compared with ibrutinib, second-generation btk inhibitors have comparable efficacy and might have a more favourable toxicity profile. Those newer btk inhibitors might therefore provide a viable treatment option for patients with r/r mcl.


Author Biographies

C. Owen, University of Calgary and Foothills Medical Centre
Division of Hematology and Hematological Malignancies
N. L. Berinstein, University of Toronto and Odette Cancer Centre, Sunnybrook Health Sciences Centre
Department of Medicine
Published
2019-04-29
How to Cite
Owen, C., Berinstein, N. L., Christofides, A., & Sehn, L. H. (2019). Review of Bruton tyrosine kinase inhibitors for the treatment of relapsed or refractory mantle cell lymphoma. Current Oncology, 26(2). https://doi.org/10.3747/co.26.4345
Section
Review Article