Characteristics of immunoglobulin gene rearrangements in vietnamese newly diagnosed multiple myeloma patients

IF 0.8 Q4 HEMATOLOGY
Leukemia Research Reports Pub Date : 2026-01-01 Epub Date: 2026-05-16 DOI:10.1016/j.lrr.2026.100594
Cao Sy Luan , Nguyen Vu Hai Son , Phan Ngo Quang Thach , Cao Van Dong , Nguyen Quoc Dung , Trinh Thuy Duong , Phu Chi Dung , Hoang Anh Vu , Phan Thi Xinh
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Abstract

Background

The immunoglobulin (IG) gene rearrangements provide valuable markers in monitoring minimal residual disease (MRD) after treatment in multiple myeloma (MM) patients. Methods: We conducted an observational study from June 2019 to June 2023. Bone marrow samples from newly diagnosed MM patients at Blood Transfusion Hematology Hospital were collected and analyzed for IG gene rearrangements. Clonal IG gene rearrangement samples were analyzed for the repertoire of rearrangements.

Results

111 newly diagnosed MM patients were collected. Bone lesions and anemia were found in 100% and 77.5% of patients, respectively. According to rISS classification, 91.9% of patients were diagnosed at an advanced stage. Cytogenetic analysis showed that 28.8% of patients expressed at least one high-risk abnormality. The most common immunophenotype of malignant plasma cells was CD38+CD138+CD19–CD56+. Noteworthily, 104 patients (93.7%) expressed at least one clonal IG gene rearrangement, while 69.4% and 18.9% of patients expressed double and triple IG gene rearrangements, respectively. VH3 and VH4 were the two most frequent among VH segments, while DH3 and JH4 were the most common among DH and JH segments, and VK1 and JK4 were the most popular repertoires in IGK gene rearrangements. KDE rearrangements were detected in 42.5% patients, and VL1 and JL3 were the most common segments in IGL gene rearrangements. Notably, the rate of clonal IGH gene rearrangements was significantly different between heavy-chain and light-chain only MM groups.

Conclusion

This is the first study in Vietnamese MM patients to comprehensively describe the characteristics of IG gene rearrangements.
越南新诊断多发性骨髓瘤患者免疫球蛋白基因重排的特点
免疫球蛋白(IG)基因重排为监测多发性骨髓瘤(MM)患者治疗后的微小残留病(MRD)提供了有价值的标志物。方法:我们于2019年6月至2023年6月进行了一项观察性研究。收集输血血液学医院新诊断的MM患者骨髓样本,分析IG基因重排。克隆IG基因重排样本进行重排库分析。结果共收集新诊断MM患者111例。骨病变和贫血的发生率分别为100%和77.5%。根据rISS分类,91.9%的患者被诊断为晚期。细胞遗传学分析显示,28.8%的患者至少表达一种高危异常。恶性浆细胞最常见的免疫表型为CD38+CD138+ CD19-CD56 +。值得注意的是,104例(93.7%)患者至少表达一次克隆性IG基因重排,69.4%和18.9%的患者分别表达两次和三次IG基因重排。VH片段中最常见的是VH3和VH4, DH和JH片段中最常见的是DH3和JH4, IGK基因重排中最常见的是VK1和JK4。42.5%的患者检测到KDE重排,VL1和JL3是IGL基因重排最常见的片段。值得注意的是,克隆性IGH基因重排率在仅重链和轻链的MM组之间存在显著差异。结论本研究首次在越南MM患者中全面描述IG基因重排的特点。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Leukemia Research Reports
Leukemia Research Reports Medicine-Oncology
CiteScore
1.70
自引率
0.00%
发文量
70
审稿时长
23 weeks
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