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意义未明的单克隆丙种球蛋白血症(MGUS)和冒烟型多发性骨髓瘤(SMM):新的生物学见解和早期治疗策略的制定。

Monoclonal gammopathy of undetermined significance (MGUS) and smoldering multiple myeloma (SMM): novel biological insights and development of early treatment strategies.

机构信息

Medical Oncology Branch, National Cancer Institute, National Institutes of Health (NIH), Bethesda, MD, USA.

出版信息

Blood. 2011 May 26;117(21):5573-81. doi: 10.1182/blood-2011-01-270140. Epub 2011 Mar 25.

Abstract

Monoclonal gammopathy of unknown significance (MGUS) and smoldering multiple myeloma (SMM) are asymptomatic plasma cell dyscrasias, with a propensity to progress to symptomatic MM. In recent years there have been improvements in risk stratification models (involving molecular markers) of both disorders, which have led to better understanding of the biology and probability of progression of MGUS and SMM. In the context of numerous molecular events and heterogeneous risk of progression, developing individualized risk profiles for patients with MGUS and SMM represents an ongoing challenge that has to be addressed by prospective clinical monitoring and extensive correlative science. In this review we discuss the current standard of care of patients with MGUS and SMM, the use of risk models, including flow cytometry and free-light chain analyses, for predicting risk of progression. Emerging evidence from molecular studies on MGUS and SMM, involving cytogenetics, gene-expression profiling, and microRNA as well as molecular imaging is described. Finally, future directions for improving individualized management of MGUS and SMM patients, as well as the potential for developing early treatment strategies designed to delay and prevent development of MM are discussed.

摘要

意义未明的单克隆丙种球蛋白血症(MGUS)和冒烟型多发性骨髓瘤(SMM)是无症状的浆细胞异常,有进展为有症状多发性骨髓瘤(MM)的倾向。近年来,这两种疾病的风险分层模型(涉及分子标志物)有所改进,这使人们更好地了解了 MGUS 和 SMM 的生物学特性和进展概率。在众多分子事件和进展的异质性风险背景下,为 MGUS 和 SMM 患者制定个体化风险概况是一个持续存在的挑战,需要通过前瞻性临床监测和广泛的相关性科学来解决。在这篇综述中,我们讨论了目前 MGUS 和 SMM 患者的治疗标准,以及使用风险模型(包括流式细胞术和游离轻链分析)来预测进展风险。描述了 MGUS 和 SMM 中涉及细胞遗传学、基因表达谱分析、microRNA 以及分子成像的分子研究的新证据。最后,讨论了改善 MGUS 和 SMM 患者个体化管理的未来方向,以及开发旨在延迟和预防 MM 发展的早期治疗策略的潜力。

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