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Prevalence, clinical aspects, and natural history of IgM MGUS

机译:IgM MGUS的患病率,临床情况和自然病史

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Background: Waldenstr?m macroglobulinemia (WM) and chronic lymphocytic leukemia (CLL) are related B-cell cancers that share several clinical and biological features. Both WM and CLL have associated precursor conditions: monoclonal gammopathy of undetermined significance (MGUS) of immunoglobulin M (IgM) type and monoclonal B-cell lymphocytosis (MBL), respectively. Recently, a case of MBL with an IgM MGUS was reported, suggesting a close biological relationship between these entities. While much is known about MGUS overall, investigations of IgM MGUS specifically have been fragmentary. Methods: In this article, we review data on the prevalence, clinical aspects and natural history of IgM MGUS, and focus on identifying gaps in our understanding of the complex relationships among B-cell malignancies and their precursors. Results: There appears to be marked heterogeneity in the prevalence of IgM MGUS across populations. However, studies have varied in definition, design, laboratory methods, and endpoints. IgM MGUS differs from non-IgM MGUS in certain respects, including prevalence across racial groups, rate of progression, and pattern of malignant outcomes. There are limited data regarding the coincident occurrence of IgM MGUS and MBL. Conclusions: Future studies incorporating both protein electrophoresis and flow cytometry are needed to define the underlying spectrum and causes of precursor development, risk factors for progression, and markers that distinguish low- and high-risk precursor patients.
机译:背景:华氏巨球蛋白血症(WM)和慢性淋巴细胞性白血病(CLL)是相关的B细胞癌,具有一些临床和生物学特征。 WM和CLL都有相关的前体疾病:免疫球蛋白M(IgM)类型的意义不明的单克隆丙种球蛋白病(MGUS)和单克隆B细胞淋巴细胞增多症(MBL)。最近,一例MBL伴有IgM MGUS的报道,表明这些实体之间存在密切的生物学关系。尽管对MGUS的总体了解很多,但对IgM MGUS的研究仍然是零碎的。方法:在本文中,我们回顾了有关IgM MGUS的患病率,临床情况和自然史的数据,并着重于确定我们对B细胞恶性肿瘤及其前体之间复杂关系的理解方面的差距。结果:IgM MGUS在人群中的患病率似乎存在明显的异质性。但是,研究在定义,设计,实验室方法和终点方面有所不同。 IgM MGUS在某些方面与非IgM MGUS有所不同,包括各个种族的患病率,进展速度和恶性结局的模式。关于同时发生IgM MGUS和MBL的数据有限。结论:未来需要结合蛋白质电泳和流式细胞术进行研究,以确定潜在的频谱和前体发育的原因,进展的风险因素以及区分低风险和高风险前体患者的标志物。

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