多发性骨髓瘤中染色体异常和bence-jones蛋白的意义

Q4 Medicine
Svetlana Krstevska Balkanov, S. Trajkova, A. Pivkova Veljanovska, D. Spasovski, N. Ridova, G. Kalcev, Irina Panovska Stavridis
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引用次数: 0

摘要

易位是导致多发性骨髓瘤(MM)的主要遗传事件之一。此外,在三分之二的MM病例中,观察到本斯琼斯蛋白的存在。本研究的目的是证明染色体异常和Bence-Jones蛋白在MM患者中发挥重要的生物标志物作用。材料和方法:本回顾性研究于2009年1月至2019年12月在北马其顿斯科普里的大学血液学诊所进行。MM患者被分为不同的治疗组:年龄小于65岁,无合并症,符合自体外周血干细胞(PBSCT)治疗条件的患者被纳入环磷酰胺-沙利度胺-地塞米松(CyThalDex)方案组。Melphalan prenisone Thalidomide (MPT)方案用于65岁以上因合并症和肾功能衰竭而不适合积极治疗方案(如PBSCT)的患者。第三组的治疗不包括新的免疫调节剂,如沙利度胺。结果:对46例MM患者进行了分子和染色体分析。分子和染色体分层MM患者的生存时间显示,高危[次二倍体(获得1q,丢失1p) Del17p, Del13q, t(11;14) t(4;14)多突变]患者占20%,存活60个月,中位生存时间为20.8个月。在具有标准风险的MM患者中,在观察期间未登记死亡结果。考虑到我们研究中的所有MM患者,35.8%的患者尿液中存在本·琼斯蛋白,而64.2%的患者尿液中未观察到本·琼斯蛋白。百分比差异具有统计学意义。结论:未来这些关键生物标志物在该疾病临床背景中的使用只能通过临床试验的仔细评估和验证来实现。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
IMPLICATIONS OF CHROMOSOMAL ABNORMALITIES AND BENCE-JONES PROTEINS IN MULTIPLE MYELOMA
Introduction: Translocations are among the main genetic events responsible for multiple myeloma (MM). Also, in two thirds of MM cases, the presence of Bence Jones proteins is observed. The aim of this study was to demonstrate the role that chromosomal abnormalities and Bence-Jones proteins play as crucial biomarkers in MM patients. Materials and Methods: This retrospective study was carried out at the University Clinic for Hematology in Skopje, North Macedonia, between January 2009 and December 2019. MM patients were divided into different treatment groups: those younger than 65 years old, without comorbidities, and eligible for autologous peripheral blood stem cells (PBSCT) were included in the Cyclophosphamide-Thalidomide-Dexamethasone (CyThalDex) protocol group. The Melphalan Prednisone Thalidomide (MPT) protocol was used in patients over the age of 65 who were unsuitable for aggressive treatment options such as PBSCT due to comorbidities and renal failure. The third group's treatment did not include new immunomodulators like thalidomide. Results: Molecular and chromosomal analyses were performed in 46 MM patients. The survival time of patients with MM concerning molecular and chromosome stratification showed that 20% of them were high-risk [hypodiploid (gain1q, loss1p) Del17p, Del13q, t(11;14) t(4;14) and multiple mutations] who survived 60 months, and the median survival time in these patients was 20.8 months. In patients with MM who had a standard risk, death outcomes were not registered during the observation period. Taking into account all MM patients included in our study, Bence Jones proteins in the urine were present in 35.8% of patients, while their presence was not observed in 64.2%. The percentage difference was statistically significant. Conclusion : The use of these critical biomarkers in the clinical background of this disease in the future can only be achieved through careful evaluation and validation in clinical trials.
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