Novel Approaches to Managing Patients with Relapsed and Refractory Waldenström Macroglobulinemia

被引:3
作者
Chohan, Karan L. [1 ]
Kapoor, Prashant [2 ]
机构
[1] Mayo Clin, Dept Med, Rochester, MN USA
[2] Mayo Clin, Div Hematol, 200 First St SW, Rochester, MN 55905 USA
关键词
Lymphoplasmacytic lymphoma; IgM monoclonal gammopathy; TYROSINE KINASE INHIBITOR; WALDENSTROM MACROGLOBULINEMIA; MULTIPLE-MYELOMA; PRIMARY THERAPY; PHASE-II; IRREVERSIBLE INHIBITOR; PROTEASOME INHIBITORS; CLINICAL-TRIAL; OPEN-LABEL; WILD-TYPE;
D O I
10.1007/s11899-024-00730-1
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Purpose of ReviewWaldenstr & ouml;m macroglobulinemia is a rare non-Hodgkin lymphoma (NHL) characterized by lymphoplasmacytic bone marrow infiltration associated with an immunoglobulin M (IgM) monoclonal gammopathy. Over the past two decades, a number of important novel therapies have emerged for the treatment of relapsed and refractory (R/R) WM. The purpose of this review is to discuss these novel agents.Recent FindingsChemoimmunotherapy which formed the basis treatment for R/R WM is slowly being replaced by novel targeted agents. These therapies, including Bruton's tyrosine kinase inhibitors, proteasome inhibitors, and B-cell lymphoma 2 inhibitors, have widened the landscape of management. Emerging therapies currently under investigation, such as bispecific T-cell engagers, chimeric antigen T-cell receptor therapy, and novel small molecule inhibitors, have additionally shown the potential to improve response and survival.SummaryThe treatment of R/R WM has greatly evolved, in large part due to a greater understanding of the biology of WM, and the evaluation of novel targeted agents in the basket trials of NHL, showing early activity in the small WM cohorts. Combination regimens with these established and emerging novel therapies have the potential to further improve disease control and induce higher rates of deep responses. Strategies aimed at altering the disease trajectory would require randomized controlled trials to provide relevant data on optimal integration and sequencing of more effective and tolerable regimens earlier in the disease course.
引用
收藏
页码:163 / 174
页数:12
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