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意义未明的单克隆免疫球蛋白轻链病的特征是在纵向分析中具有较高的消失率和较低的进展风险。

Light chain monoclonal gammopathy of undetermined significance is characterized by a high disappearance rate and low risk of progression on longitudinal analysis.

机构信息

Institute of Medical Informatics, Biometry and Epidemiology, University Hospital Essen, Essen, Germany.

Department of Hematology, University Hospital Essen, Hufelandstr. 55, D-45122, Essen, Germany.

出版信息

Ann Hematol. 2018 Aug;97(8):1463-1469. doi: 10.1007/s00277-018-3305-x. Epub 2018 Apr 9.

Abstract

We determined the 10-year progression rate of light chain monoclonal gammopathy of undetermined significance (LCMGUS) and investigated potential associations with cancer utilizing the German population-based Heinz Nixdorf Recall Study. The Heinz Nixdorf Recall Study comprises 4814 men and women aged 45-75 years. Serum samples from baseline (2000-2003) and five-year (2006-2008) and 10-year (2011-2015) follow-up examinations were screened for monoclonal free light chains (FLC). LCMGUS was defined as abnormal FLC ratio, increase of involved FLC with complete loss of immunoglobulin heavy chain, and absence of a history of lymphoproliferative disease (LPD). Seventy-five individuals with LCMGUS were identified across all three evaluation time points (median age 64 years; 43 (57%) male; FLCR > 1.65 65 (87%); FLCR ≤ 0.65 10 (13%)). After a median observation time of 11.5 years, none of the LCMGUS cases had progressed to overt LPD; in particular, we did not observe incident light chain multiple myeloma. On serial analysis 17/31 (55%), LCMGUS could not be confirmed and disappearance of the monoclonal protein was associated with low concentrations of the involved FLC. Individuals with LCMGUS had a 1.5-fold increased risk of cancer but did not show differences in overall survival or renal function as compared to individuals with normal FLC. In conclusion, LCMGUS represents a relatively benign condition with a high disappearance rate of the monoclonal protein on longitudinal analysis and normal overall survival at least in the population-based setting.

摘要

我们通过德国基于人群的 Heinz Nixdorf 召回研究,确定了意义未明的单克隆轻链γ球蛋白病(LCMGUS)的 10 年进展率,并研究了其与癌症的潜在关联。Heinz Nixdorf 召回研究包括 4814 名年龄在 45-75 岁的男性和女性。在基线(2000-2003 年)和 5 年(2006-2008 年)和 10 年(2011-2015 年)随访检查时,对血清样本进行了单克隆游离轻链(FLC)筛查。LCMGUS 的定义为异常 FLC 比值、受累 FLC 增加伴免疫球蛋白重链完全丢失,且无淋巴增殖性疾病(LPD)病史。在所有三个评估时间点均发现了 75 例 LCMGUS 患者(中位年龄 64 岁;43 例[57%]为男性;FLCR>1.65 65 例[87%];FLCR≤0.65 10 例[13%])。中位观察时间为 11.5 年后,LCMGUS 病例均未进展为显性 LPD;特别是,我们未观察到新发的轻链多发性骨髓瘤。在连续分析中,17/31(55%)例 LCMGUS 无法得到确认,且单克隆蛋白的消失与受累 FLC 的低浓度相关。LCMGUS 患者的癌症风险增加了 1.5 倍,但与 FLC 正常的患者相比,其总体生存率或肾功能无差异。总之,在基于人群的研究中,LCMGUS 代表了一种相对良性的疾病,在纵向分析中其单克隆蛋白的消失率较高,且总体生存率正常。

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