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Smoldering (asymptomatic) multiple myeloma: revisiting the clinical dilemma and looking into the future.冒烟型(无症状性)多发性骨髓瘤:重新审视临床困境并展望未来。
Clin Lymphoma Myeloma Leuk. 2010 Aug;10(4):248-57. doi: 10.3816/CLML.2010.n.053.
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Monoclonal gammopathy of undetermined significance and risk of skeletal fractures: a population-based study.意义未明的单克隆丙种球蛋白血症与骨骼骨折风险:一项基于人群的研究。
Blood. 2010 Oct 14;116(15):2651-5. doi: 10.1182/blood-2010-04-282848. Epub 2010 Jul 7.
3
Bone marrow microenvironment in myelomagenesis: its potential role in early diagnosis.骨髓微环境在骨髓瘤发生中的作用:其在早期诊断中的潜在作用。
Expert Rev Mol Diagn. 2010 May;10(4):465-80. doi: 10.1586/erm.10.31.
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Obesity is associated with an increased risk of monoclonal gammopathy of undetermined significance among black and white women.肥胖与黑人和白人女性中意义未明的单克隆丙种球蛋白病的风险增加有关。
Blood. 2010 Aug 19;116(7):1056-9. doi: 10.1182/blood-2010-01-262394. Epub 2010 Apr 26.
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Monoclonal gammopathy of undetermined significance (MGUS) and smoldering (asymptomatic) multiple myeloma: IMWG consensus perspectives risk factors for progression and guidelines for monitoring and management.意义未明的单克隆丙种球蛋白血症(MGUS)和冒烟型(无症状)多发性骨髓瘤:IMWG 共识观点——进展风险因素以及监测和管理指南。
Leukemia. 2010 Jun;24(6):1121-7. doi: 10.1038/leu.2010.60. Epub 2010 Apr 22.
6
Arterial and venous thrombosis in monoclonal gammopathy of undetermined significance and multiple myeloma: a population-based study.意义未明的单克隆丙种球蛋白血症和多发性骨髓瘤中的动静脉血栓形成:一项基于人群的研究。
Blood. 2010 Jun 17;115(24):4991-8. doi: 10.1182/blood-2009-11-252072. Epub 2010 Mar 18.
7
Gene expression profiling of bone marrow endothelial cells in patients with multiple myeloma.多发性骨髓瘤患者骨髓内皮细胞的基因表达谱分析
Clin Cancer Res. 2009 Sep 1;15(17):5369-78. doi: 10.1158/1078-0432.CCR-09-0040. Epub 2009 Aug 18.
8
Gene expression profiles of tumor biology provide a novel approach to prognosis and may guide the selection of therapeutic targets in multiple myeloma.肿瘤生物学的基因表达谱为预后提供了一种新方法,并可能指导多发性骨髓瘤治疗靶点的选择。
J Clin Oncol. 2009 Sep 1;27(25):4197-203. doi: 10.1200/JCO.2008.19.1916. Epub 2009 Jul 27.
9
Patterns of survival and causes of death following a diagnosis of monoclonal gammopathy of undetermined significance: a population-based study.不明意义单克隆丙种球蛋白血症诊断后的生存模式和死亡原因:一项基于人群的研究。
Haematologica. 2009 Dec;94(12):1714-20. doi: 10.3324/haematol.2009.010066. Epub 2009 Jul 16.
10
Patterns of monoclonal gammopathy of undetermined significance and multiple myeloma in various ethnic/racial groups: support for genetic factors in pathogenesis.不同种族/民族群体中意义未明的单克隆丙种球蛋白病和多发性骨髓瘤的模式:对发病机制中遗传因素的支持
Leukemia. 2009 Oct;23(10):1691-7. doi: 10.1038/leu.2009.134. Epub 2009 Jul 9.

意义未明的单克隆丙种球蛋白血症和冒烟型骨髓瘤:对发病机制和流行病学的新认识。

Monoclonal gammopathy of undetermined significance and smoldering myeloma: new insights into pathophysiology and epidemiology.

机构信息

Multiple Myeloma Section, Medical Oncology Branch, Center for Cancer Research, National Cancer Institute, National Institutes of Health, Bethesda, Maryland 20892, USA.

出版信息

Hematology Am Soc Hematol Educ Program. 2010;2010:295-302. doi: 10.1182/asheducation-2010.1.295.

DOI:10.1182/asheducation-2010.1.295
PMID:21239809
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7384383/
Abstract

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?

摘要

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?