The Direction of Modern Therapies in Waldenström Macroglobulinaemia

Waldenström macroglobulinaemia (WM) is a rare lymphoplasmacytic disease that is hallmarked by B-cell infiltration of the bone marrow, an overexpression of IgM class antibodies and an activating mutation of MYD88 (L265P). The therapeutic options for WM patients include a combination of Rituximab (anti-CD20 monoclonal antibody) and chemotherapy, with newer treatments like proteasomal inhibitors and Bruton's Tyrosine Kinase (BTK) inhibitors showing high levels of success both as monotherapy and in combinations. To date, WM remains incurable. Understanding the basic physiology of WM and creating new and improved pre-clinical models which better reflect the true physiology of WM will allow for the identification of novel therapeutic vulnerabilities and the ability to test these next generation therapies, both in a tumour intrinsic and extrinsic manner. In this review, we aim to provide a comprehensive summary of WM, focusing on the genetic mutations and signalling pathways driving disease progression. In addition, we highlight the current therapeutics and emerging clinical trials to provide novel insights to drive deep and durable responses.

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Publication Details

Journal
Journal of Cellular and Molecular Medicine
Published
2025-12-01
DOI
https://doi.org/10.1111/jcmm.70987
Primary Topic
Chronic Lymphocytic Leukemia Research
Type
article
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article

The Direction of Modern Therapies in Waldenström Macroglobulinaemia

Stephen Blackmore, Sherine F. Elsawa, Omid Tavana
Journal of Cellular and Molecular Medicine
Chronic Lymphocytic Leukemia Research
article

The Direction of Modern Therapies in Waldenström Macroglobulinaemia

Stephen Blackmore, Sherine F. Elsawa, Omid Tavana
article en

Abstract

Waldenström macroglobulinaemia (WM) is a rare lymphoplasmacytic disease that is hallmarked by B-cell infiltration of the bone marrow, an overexpression of IgM class antibodies and an activating mutation of MYD88 (L265P). The therapeutic options for WM patients include a combination of Rituximab (anti-CD20 monoclonal antibody) and chemotherapy, with newer treatments like proteasomal inhibitors and Bruton's Tyrosine Kinase (BTK) inhibitors showing high levels of success both as monotherapy and in combinations. To date, WM remains incurable. Understanding the basic physiology of WM and creating new and improved pre-clinical models which better reflect the true physiology of WM will allow for the identification of novel therapeutic vulnerabilities and the ability to test these next generation therapies, both in a tumour intrinsic and extrinsic manner. In this review, we aim to provide a comprehensive summary of WM, focusing on the genetic mutations and signalling pathways driving disease progression. In addition, we highlight the current therapeutics and emerging clinical trials to provide novel insights to drive deep and durable responses.

Journal of Cellular and Molecular MedicineVol. 29(24)
University of New Hampshire (US), AstraZeneca (South Korea) (KR), AstraZeneca (Brazil) (BR), AstraZeneca (United States) (US)
Openalex Percentile: Top 26%
Chronic Lymphocytic Leukemia Research
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