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A novel biomarker score for the screening and management of patients with plasma cell proliferative disorders

机译:用于筛查和处理浆细胞增生性疾病患者的新型生物标志物评分

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OBJECTIVE: Monoclonal plasma cell proliferative disorders comprise a wide spectrum of diseases associated to clonal B-cell expansion. Serum protein electrophoretic profile (SPEP) and circulating free light chains (FLCs) levels are the mainstay of diseases management. Recently, soluble (s) Syndecan-1 (SDC1, CD138) produced by myeloma plasma cells has been suggested in the monitoring and follow-up of patients with myeloma. The aim of our study is to evaluate sCD138 in addition with FLCs and SPEP for the screening of patients with different evolutive disease pathways. PATIENTS AND METHODS: Sera from 73 patients with monoclonal gammopathy of undetermined significance (MGUS), 120 smoldering and 42 multiple myeloma (SMM and MM, respectively), 70 HCV-related mixed cryoglobulinemia (MC), 35 B-cell non-Hodgkin’s lymphoma (B-NHL) and sera from 50 healthy donors (HD), were tested for sCD138, FLCs (assessed by means of ELISA and turbidimetric assay, respectively) and electrophoresis pattern (performed on Capillarys system) for the generation of a novel biomarker score (BS). RESULTS: Our results were grouped according to the two main lines of disease progression (vs. MM or B-NHL): in one group we found BS mean values of 0.2, 3.4, 5.3, 7.1 for HD, MGUS, SMM and MM, respectively; in the other group of 0.2, 4.4, 6.7 for HD, MC and B-NHL. CONCLUSIONS: We showed that BS mean values follow the ingravescence disease status towards the two main lines of progression to cancerous conditions; it could represent an additional useful tool in the management of screening and/or follow-up.
机译:目的:单克隆浆细胞增生性疾病包括与克隆B细胞扩增相关的多种疾病。血清蛋白电泳图谱(SPEP)和循环游离轻链(FLCs)水平是疾病管理的主要内容。近来,已经建议由骨髓瘤浆细胞产生的可溶性Syndecan-1(SDC1,CD138)用于骨髓瘤患者的监测和随访中。我们研究的目的是评估sCD138以及FLC和SPEP,以筛查具有不同进化性疾病途径的患者。患者和方法:来自73例意义不明的单克隆丙种球蛋白病(MGUS),120闷烧和42例多发性骨髓瘤(分别为SMM和MM),70 HCV相关混合性冷球蛋白血症(MC),35 B细胞非霍奇金淋巴瘤测试了来自50位健康供体(HD)的(B-NHL)和血清的sCD138,FLC(分别通过ELISA和比浊法评估)和电泳图谱(在Capillarys系统上执行)以产生新的生物标记(BS)。结果:我们的结果根据疾病进展的两个主要方面(相对于MM或B-NHL)进行分组:在一组中,我们发现HD,MGUS,SMM和MM的BS平均值分别为0.2、3.4、5.3、7.1,分别;在HD,MC和B-NHL的另一组中分别为0.2、4.4、6.7。结论:我们显示BS平均值遵循向疾病进展的两条主要路线的渐进疾病状态。它可以代表筛查和/或随访管理中的另一个有用工具。

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