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首页> 外文期刊>Oncology >Management of Monoclonal Gammopathy of Undetermined Significance (MGUS) and Smoldering Multiple Myeloma (SMM)
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Management of Monoclonal Gammopathy of Undetermined Significance (MGUS) and Smoldering Multiple Myeloma (SMM)

机译:未定意义的单克隆丙种球蛋白病(MGUS)和阴燃性多发性骨髓瘤(SMM)的管理

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摘要

Monoclonal gammopathy of undetermined significance (MGUS) is defined as a serum M protein level of less than 3 g/dL, less than 10% clonal plasma cells in the bone marrow, and the absence of end-organ damage. The prevalence of MGUS is 3.2% in the white population but is approximately twice that high in the black population. MGUS may progress to multiple myeloma, AL amyloidosis, Waldenstrom macroglobulinemia, or lymphoma. The risk of progression is approximately 1% per year, but the risk continues even after more than 25 years of observation. Risk factors for progression include the size of the serum M protein, the type of serum M protein, the number of plasma cells in the bone marrow, and the serum free light chain ratio. Smoldering (asymptomatic) multiple myeloma (SMM) is characterized by the presence of an M protein level of 3 g/dL or higher and/or 10% or more monoclonal plasma cells in the bone marrow but no evidence of end-organ damage. The overall risk of progression to a malignant condition is 10% per year for the first 5 years, approximately 3% per year for the next 5 years, and 1 % to 2% per year for the following 10 years. Patients with both MGUS and SMM must be followed up for their lifetime.
机译:意义未定的单克隆丙种球蛋白病(MGUS)定义为血清M蛋白水平低于3 g / dL,骨髓中克隆浆细胞低于10%,并且不存在终末器官损害。 MGUS在白人人群中的患病率为3.2%,但在黑人人群中的患病率约为后者的两倍。 MGUS可能进展为多发性骨髓瘤,AL淀粉样变性,Waldenstrom巨球蛋白血症或淋巴瘤。进展的风险约为每年1%,但是即使经过25年以上的观察,风险仍会持续。进展的危险因素包括血清M蛋白的大小,血清M蛋白的类型,骨髓中的浆细胞数量以及血清游离轻链比率。闷烧(无症状)多发性骨髓瘤(SMM)的特征是骨髓中存在3 g / dL或更高和/或10%或更多的单克隆浆细胞M蛋白水平,但没有端器官损害的证据。进展为恶性疾病的总风险在前5年为每年10%,在接下来的5年为每年3%,在接下来的10年为每年1%至2%。 MGUS和SMM病人必须终生随访。

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