Multiple Myeloma Section, Medical Oncology Branch, Center for Cancer Research, National Cancer Institute, National Institutes of Health, Bethesda, Maryland 20892, USA.
Hematology Am Soc Hematol Educ Program. 2010;2010:295-302. doi: 10.1182/asheducation-2010.1.295.
Routine screening for monoclonal gammopathy of undetermined significance (MGUS) is not indicated. Despite this fact, MGUS is a common finding in medical practice. Almost all individuals diagnosed with MGUS represent incidental cases diagnosed when physicians order serum protein electrophoresis, immunofixation, or both, as part of the work-up of a number of common symptoms and laboratory abnormalities. In the absence of reliable molecular predictors of outcome, the detection of an early precursor state typically imposes a complex situation for the patient and the responsible physician-usually, it leads to a lot of questions that lack clear answers. In the past years, several novel insights have been gained in the area of multiple myeloma (MM) precursor disease. This review focuses on results from recent investigations and discusses implications for diagnostic work-up, clinical management, and patient counseling. More specifically, it sheds light on the following commonly asked questions by patients and physicians: i) what is the risk of progression from precursor to full-blown MM, and are there ways to risk-stratify patients?; ii) is MM always preceded by a precursor state, and is there anything that could or should be done to delay or prevent progression?; and iii) why do some individuals develop MM precursor diseases, and is there a reason to screen the family?
对意义未明的单克隆丙种球蛋白血症(MGUS)进行常规筛查并不合适。尽管如此,MGUS 在医学实践中还是很常见的。几乎所有被诊断为 MGUS 的患者都是偶然发现的,这些患者在医生对一系列常见症状和实验室异常进行检查时,会要求进行血清蛋白电泳、免疫固定或两者同时进行,从而被诊断出患有 MGUS。由于缺乏可靠的预后分子预测指标,早期前驱状态的检出通常会给患者和负责的医生带来复杂的情况——通常会导致很多问题,而这些问题缺乏明确的答案。在过去的几年中,多发性骨髓瘤(MM)前驱疾病领域取得了一些新的认识。本综述重点介绍了最近的研究结果,并讨论了其对诊断检查、临床管理和患者咨询的影响。更具体地说,它阐明了患者和医生经常问到的以下问题:i)从前驱状态进展为完全 MM 的风险是多少,是否有办法对患者进行风险分层?;ii)MM 总是由前驱状态引起的吗,是否有办法延缓或阻止进展?;以及 iii)为什么有些人会患上 MM 前驱疾病,是否有理由对其家族进行筛查?