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冒烟型多发性骨髓瘤治疗的最新进展

Recent Advances in the Management of Smoldering Multiple Myeloma.

作者信息

Madhira Bhaskara Reddy, Konala Venu Madhav, Adapa Sreedhar, Naramala Srikanth, Ravella Pavan Mahendra, Parikh Kaushal, Gentile Teresa C

机构信息

SUNY Upstate Medical University, Syracuse, NY, USA.

Ashland Bellefonte Cancer Center, Ashland, KY, USA.

出版信息

World J Oncol. 2020 Apr;11(2):45-54. doi: 10.14740/wjon1245. Epub 2020 Mar 29.

Abstract

There is remarkable progress in the treatment of multiple myeloma (MM) with significant improvement in survival in the past 10 years. Monoclonal gammopathy of undetermined significance (MGUS) and smoldering multiple myeloma (SMM) can evolve into symptomatic multiple myeloma (sy-MM) with organ involvement. SMM has associated with a much higher progression to MM compared to MGUS. In 2014, International Myeloma Working Group (IMWG) reclassified ultra-high-risk smoldering myeloma patients with bone marrow plasma cells > 60% or serum-free light chain ratio (FLCr) > 100 or > 1 focal bone lesion on the magnetic resonance imaging as MM. SMM is a heterogeneous disorder with probability for progression to myeloma up to 50% in the first 5 years. Several risk models and clinical features have been identified to stratify the risk of progression to MM. Thanks to advances in our understanding of the genomic profile of MM, there are several ongoing clinical trials, and genomic studies are being done to assess the risk of progression to MM and early intervention. There is still no standard criterion regarding when to start therapy. This review discusses identifying SMM patients who are at high risk of progression to sy-MM and recent development of new and early treatment strategies and ongoing clinical trials for these high-risk SMM patients.

摘要

在过去10年中,多发性骨髓瘤(MM)的治疗取得了显著进展,生存率有了显著提高。意义未明的单克隆丙种球蛋白病(MGUS)和冒烟型多发性骨髓瘤(SMM)可发展为有器官受累的症状性多发性骨髓瘤(sym-MM)。与MGUS相比,SMM进展为MM的可能性要高得多。2014年,国际骨髓瘤工作组(IMWG)将骨髓浆细胞>60%或血清游离轻链比值(FLCr)>100或磁共振成像上有>1处局灶性骨病变的超高风险冒烟型骨髓瘤患者重新分类为MM。SMM是一种异质性疾病,在最初5年内进展为骨髓瘤的概率高达50%。已经确定了几种风险模型和临床特征来对进展为MM的风险进行分层。由于我们对MM基因组特征的理解取得了进展,目前有几项正在进行的临床试验,并且正在进行基因组研究以评估进展为MM的风险和早期干预情况。关于何时开始治疗仍然没有标准标准。本综述讨论了识别进展为sym-MM风险高的SMM患者以及新的早期治疗策略的最新进展和针对这些高风险SMM患者正在进行的临床试验。

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