Progress in the Management of Smoldering Multiple Myeloma.

IF 2.7 3区 医学 Q2 HEMATOLOGY
Current Hematologic Malignancy Reports Pub Date : 2021-04-01 Epub Date: 2021-05-13 DOI:10.1007/s11899-021-00623-7
Timothy M Schmidt, Natalie S Callander
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引用次数: 2

Abstract

Purpose of review: Smoldering multiple myeloma (SMM) is defined as an asymptomatic clonal proliferation of pre-malignant plasma cells and an increased risk of progression to multiple myeloma (MM) relative to monoclonal gammopathy of undetermined significance. Whether patients with SMM should be treated prior to development of symptomatic disease is fiercely debated and is a highly active area of research.

Recent findings: The ECOG E3A06 study demonstrated that early treatment with lenalidomide significantly reduced the risk of progression to MM compared to observation in patients with high risk SMM. The IMWG recently validated a risk stratification model to include cytogenetics and a personalized risk calculator for individual patients. Beyond this, molecular genomic aberrations and immunological phenomena that promote progression from asymptomatic disease to MM have been recently characterized and may help to more precisely identify patients who are most suitable for early intervention. As highly effective and tolerable therapies for plasma cell disorders evolve, the field is approaching a paradigm shift that involves the adoption of intervention for patients with SMM who are at high risk for progression to symptomatic myeloma in order to prevent morbidity and mortality. This review highlights our current understanding of the biology of patients with SMM, clarifies the rationale for early intervention, and summarizes early results of various treatment strategies for patients with high-risk smoldering myeloma.

阴燃性多发性骨髓瘤的治疗进展。
综述目的:阴燃型多发性骨髓瘤(SMM)被定义为恶性前浆细胞的无症状克隆性增殖,相对于意义不明的单克隆伽玛病,其进展为多发性骨髓瘤(MM)的风险增加。SMM患者是否应该在症状性疾病发展之前进行治疗是一个激烈的争论,也是一个高度活跃的研究领域。最近的发现:ECOG E3A06研究表明,与观察高危SMM患者相比,早期使用来那度胺治疗可显著降低进展为MM的风险。IMWG最近验证了一种风险分层模型,该模型包括细胞遗传学和个体患者的个性化风险计算器。除此之外,促进从无症状疾病发展为MM的分子基因组畸变和免疫现象最近得到了表征,可能有助于更准确地确定最适合早期干预的患者。随着高效且耐受的浆细胞疾病治疗方法的发展,该领域正在接近一个范式转变,包括对进展为症状性骨髓瘤的高风险SMM患者采用干预措施,以防止发病率和死亡率。这篇综述强调了我们目前对SMM患者生物学的理解,阐明了早期干预的基本原理,并总结了高风险阴燃骨髓瘤患者的各种治疗策略的早期结果。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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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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