AI Article Synopsis

  • Waldenström macroglobulinaemia (WM) is a slow-growing B-cell cancer characterized by high levels of IgM protein, specific bone marrow changes, and a prevalent mutation (MYD88 L265P) found in most patients.
  • Traditional treatment has involved chemoimmunotherapy, but recent research highlights the effectiveness of Bruton tyrosine kinase inhibitors as a standalone treatment or alongside other drugs.
  • The Medical and Scientific Advisory Group of Myeloma Australia has updated recommendations for managing WM, incorporating recent evidence and advancements in treatment options since their last report in 2017.

Article Abstract

Waldenström macroglobulinaemia (WM) is an indolent B-cell malignancy characterised by the presence of IgM paraprotein, bone marrow infiltration by clonal small B lymphocytes with plasmacytic differentiation and the MYD88 L265P mutation in >90% of cases. Traditionally, WM has been treated with chemoimmunotherapy. Recent trials have demonstrated the efficacy and safety of Bruton tyrosine kinase inhibitors in WM, both as monotherapy and in combination with other drugs. There is emerging evidence on the use of other agents including B-cell lymphoma 2 inhibitors and on the treatment of rare presentations of WM. In this update, the Medical and Scientific Advisory Group of Myeloma Australia reviews the available evidence on the treatment of WM since the last publication in 2017 and provides specific recommendations to assist Australian clinicians in the management of this disease.

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http://dx.doi.org/10.1111/imj.15980DOI Listing

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