Abstract
Waldenström’s macroglobulinemia (WM) is a distinct B-cell lymphoproliferative disorder for which clearly defined criteria for the diagnosis, initiation of therapy, and treatment strategy have been proposed as part of the consensus panels of the International Workshops on WM (IWWM). Therapeutic strategies in WM should be based on individual patient and disease characteristics. Chemoimmunotherapy combinations with rituximab (R) and cyclophosphamide/dexamethasone (DRC) or bendamustine (Benda-R) or bortezomib/dexamethasone (BDR) provide durable responses and are still indicated in most patients. The approval of the BTK-inhibitor ibrutinib in the USA and in Europe represents a novel and effective treatment option for both treatment-naïve and relapsing patients. Other BCR inhibitors, second-generation proteasome inhibitors (e.g., carfilzomib), and mTOR inhibitors are promising and may expand future treatment options. This chapter summarizes the treatment strategies in WM patients with the treatment options widely described by previous authors.
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References
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Leblond, V., Dimopoulos, M.A., Treon, S.P. (2017). Treatment Recommendations in Waldenström Macroglobulinemia. In: Leblond, V., Treon, S., Dimoploulos, M. (eds) Waldenström’s Macroglobulinemia. Springer, Cham. https://doi.org/10.1007/978-3-319-22584-5_26
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DOI: https://doi.org/10.1007/978-3-319-22584-5_26
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