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多发性骨髓瘤中枢神经系统受累的临床特征、治疗模式及预后:一项来自中国的多中心回顾性研究

英文原题:Clinical Characteristics, Treatment Patterns, and Prognosis of Central Nervous System Involvement in Multiple Myeloma: A Multicenter Retrospective Study From China.

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Clinical Characteristics, Treatment Patterns, and Prognosis of Central Nervous System Involvement in Multiple Myeloma: A Multicenter Retrospective Study From China.

PubMed 2026/06/01(内容时间) Cancer Med Q2 · IF 3.5(JCR 2025)

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研究概要

多发性骨髓瘤的中枢神经系统受累与疾病侵袭性强和预后不良相关。

中文摘要

中枢神经系统(CNS)受累是多发性骨髓瘤(MM)罕见且侵袭性强的并发症,其临床特征和预后数据有限。本多中心研究描述迄今规模最大的中国MM中枢神经系统受累(MM-CNS)患者队列。

我们在中国9家血液病中心开展多中心回顾性研究(2017年7月至2024年6月),分析MM-CNS患者的临床记录。收集诊断参数、治疗方案和生存结局。

在识别出的35例MM-CNS患者中,中位年龄为55岁(范围40–83岁)。31.4%(11/35)在MM初诊时出现CNS表现,68.6%(24/35)在复发时出现;从MM确诊至CNS受累的中位时间为22.8个月。主要特征包括IgG亚型(51.4%)、轻链限制(54.3%)和高危细胞遗传学异常:1q21扩增(48.3%)、t(4;14)易位(13.8%)及复杂核型(35.7%)。诊断通过脑脊液分析(蛋白升高、检出浆细胞)与神经影像(脑膜/脑实质病灶)共同确认。治疗包括全身化疗(88.6%)、鞘内治疗(51.4%)、放疗(17.1%)、CAR-T 细胞治疗(11.4%)和自体干细胞移植(ASCT,14.3%)。尽管总体缓解率为62.9%(完全缓解率36.4%),仍有56%的患者在中位3.1个月内复发(范围1.2–8.4个月)。中位随访时间为19.1个月(范围0.1–46.8个月)。报告的中位总生存期为13.0个月(范围0.1–43.1个月),死亡率为60%(21/35)。

MM累及CNS与疾病侵袭性强及预后不良相关。多模式治疗虽可带来短暂应答,但快速进展和高死亡率仍持续存在。亟需新策略改善这一高危人群的结局。

展开英文摘要原文

Central nervous system (CNS) involvement is a rare and aggressive complication of multiple myeloma (MM), with limited data on its clinical characteristics and prognosis. This multicenter study characterizes the largest Chinese cohort of MM patients with CNS involvement (MM-CNS) to date.

We conducted a multicenter retrospective study across nine hematology centers in China (July 2017-June 2024), analyzing clinical records of MM-CNS patients. Data collection encompassed diagnostic parameters, treatment regimens, and survival outcomes.

Among 35 identified MM-CNS cases (median age 55 years, range 40-83), CNS manifestations presented at initial MM diagnosis in 31.4% (11/35) versus relapse in 68.6% (24/35), with median latency of 22.8 months from MM diagnosis. Predominant features included IgG subtype (51.4%), light chain restriction (54.3%), and high-risk cytogenetics: 1q21 amplification (48.3%), t(4;14) translocation (13.8%), and complex karyotypes of chromosome (35.7%). Diagnostic confirmation combined CSF analysis (protein elevation, plasma cell detection) with neuroimaging (meningeal/parenchymal lesions). Treatments included systemic chemotherapy (88.6%), intrathecal therapy (51.4%), radiotherapy (17.1%), chimeric antigen receptor T-cell (CAR-T) therapy (11.4%), and autologous stem cell transplantation (ASCT) (14.3%). Despite 62.9% overall response rate (36.4% complete remission), 56% relapsed within median 3.1 months (range 1.2-8.4). The median follow-up duration was 19.1 months (range: 0.1-46.8). Median overall survival (OS) at 13.0 months (range 0.1-43.1) with 60% mortality (21/35).

CNS involvement in MM is associated with aggressive disease and poor prognosis. Despite transient responses to multimodal therapies, rapid progression and high mortality persist. Novel strategies are urgently needed to improve outcomes in this high-risk population.

论文信息

作者
Li W、Tian W、Ma J、Li L、Li Z、Liu J、Gao G、Xi Z
单位
Department of Hematology, Myeloma Research Center of Beijing, Beijing Chaoyang Hospital, Capital Medical University, Beijing, China.China
文献类型
多中心研究
期刊
Cancer medicine2026 Jun
原文标识
PubMed 42204788 · DOI 10.1002/cam4.71986