Novel Approaches to Managing Patients with Relapsed and Refractory Waldenström Macroglobulinemia.

IF 2.7 3区 医学 Q2 HEMATOLOGY Current Hematologic Malignancy Reports Pub Date : 2024-08-01 Epub Date: 2024-07-06 DOI:10.1007/s11899-024-00730-1
Karan L Chohan, Prashant Kapoor
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Abstract

Purpose of review: Waldenström 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 findings: Chemoimmunotherapy 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. The 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.

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治疗复发性和难治性瓦尔登斯特伦巨球蛋白血症患者的新方法
审查目的:瓦尔登斯特伦巨球蛋白血症是一种罕见的非霍奇金淋巴瘤(NHL),其特点是淋巴浆细胞性骨髓浸润,伴有免疫球蛋白M(IgM)单克隆丙种球蛋白病。过去二十年来,治疗复发性和难治性(R/R)WM 的一些重要新型疗法不断涌现。本综述旨在讨论这些新型药物:化疗免疫疗法是治疗复发性和难治性(R/R)WM 的基础疗法,目前正逐渐被新型靶向药物所取代。这些疗法包括布鲁顿酪氨酸激酶抑制剂、蛋白酶体抑制剂和B细胞淋巴瘤2抑制剂,拓宽了治疗范围。目前正在研究的新疗法,如双特异性T细胞啮合剂、嵌合抗原T细胞受体疗法和新型小分子抑制剂,也显示出改善反应和生存的潜力。对 R/R WM 的治疗有了很大的发展,这在很大程度上是由于对 WM 的生物学特性有了更深入的了解,以及在 NHL 篮子试验中对新型靶向药物进行了评估,在小型 WM 队列中显示出早期活性。这些既有疗法和新出现的新型疗法的联合疗法有可能进一步改善疾病控制并诱导更高的深度反应率。旨在改变疾病轨迹的策略需要进行随机对照试验,以提供相关数据,说明如何在病程早期对更有效、更耐受的疗法进行最佳整合和排序。
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来源期刊
CiteScore
6.00
自引率
0.00%
发文量
28
审稿时长
>12 weeks
期刊介绍: his journal intends to provide clear, insightful, balanced contributions by international experts that review the most important, recently published clinical findings related to the diagnosis, treatment, management, and prevention of hematologic malignancy. We accomplish this aim by appointing international authorities to serve as Section Editors in key subject areas, such as leukemia, lymphoma, myeloma, and T-cell and other lymphoproliferative malignancies. Section Editors, in turn, select topics for which leading experts contribute comprehensive review articles that emphasize new developments and recently published papers of major importance, highlighted by annotated reference lists. An international Editorial Board reviews the annual table of contents, suggests articles of special interest to their country/region, and ensures that topics are current and include emerging research. Commentaries from well-known figures in the field are also provided.
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