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放疗在诊断性挑战的颅内浆细胞瘤中的临床获益增强:190 例分析。

Enhanced clinical outcomes with radiotherapy in diagnostically challenging intracranial plasmacytomas: Analysis of 190 cases.

机构信息

Department of Neurosurgery, Huashan Hospital, Fudan University, Shanghai, China.

National Center for Neurological Disorders, Shanghai, China.

出版信息

Cancer Med. 2024 Feb;13(4):e7017. doi: 10.1002/cam4.7017.

Abstract

BACKGROUND

Intracranial plasmacytomas are rare tumors arising from plasma cells with approximately half of the cases progressing to multiple myeloma (MM). However, there is a lack of comprehensive clinical cohort analysis on the clinical and pathological features, progression, and outcomes of intracranial plasmacytomas.

METHODS

A retrospective analysis of 190 cases was conducted, combining data from 38 cases in a single institution and 152 cases from the literature. Patient demographics, clinical presentations, tumor locations, imaging features, surgical treatments, and follow-up outcomes were collected and analyzed. Survival analysis and Cox regression analysis were performed to identify prognostic factors.

RESULTS

A total of 190 intracranial plasmacytoma patients with an average age of 55.4 years were included in the study. The preoperative misdiagnosis ratio was high at 55.3%, and 59.7% of the tumors affected the calvaria convexity, compared to 40.3% located at the skull base. Resection and biopsy were achieved in 72.4% and 27.6% patients, respectively. Among them, 34.2% (65/190) of patients were initially diagnosed with MM with intracranial plasmacytoma as their first presentation (MM-IPFP), while 63.2% (120/190) of patients were diagnosed with solitary intracranial plasmacytoma (SIP), including 61 extramedullary plasmacytomas and 59 solitary bone plasmacytomas. In the SIP group, 22.4% (24/107) of patients experienced disease progression leading to the development of MM during a median follow-up time of 42.6 months (range 1-230 months). Multivariate analysis unveiled that radiotherapy (HR, 0.05; 95% CI, 0.00-0.87; p = 0.04), not surgery, was a protective prognostic factor for overall survival in MM-IPFP patients. Comparison between the SIP progression group and non-progression group revealed a significant difference of Ki-67 index (non-progression vs. SIP progression, 8.82% ± 7.03 vs. 16.5% ± 10.5, p < 0.05). AUC analysis determined that a cutoff value of 9.0% was the best predictor of SIP progression, with an area under the curve of 0.712.

CONCLUSIONS

This retrospective clinical analysis highlights the potential role of radiotherapy, rather than surgical resection, in improving the outcomes of intracranial plasmacytoma. Additionally, the Ki-67 index is identified as a valuable marker for predicting disease progression. This would provide some evidence for the paradigm of diagnosis and treatment modalities for intracranial plasmacytomas from the large cohort.

摘要

背景

颅内浆细胞瘤是一种罕见的肿瘤,起源于浆细胞,大约一半的病例会进展为多发性骨髓瘤(MM)。然而,目前缺乏对颅内浆细胞瘤的临床和病理特征、进展和结局进行全面的临床队列分析。

方法

对 190 例患者进行回顾性分析,结合了单机构的 38 例患者和文献中的 152 例患者的数据。收集并分析了患者的人口统计学、临床表现、肿瘤位置、影像学特征、手术治疗和随访结果。进行生存分析和 Cox 回归分析以确定预后因素。

结果

本研究共纳入 190 例颅内浆细胞瘤患者,平均年龄为 55.4 岁。术前误诊率为 55.3%,59.7%的肿瘤影响颅盖凸面,而 40.3%位于颅底。分别有 72.4%和 27.6%的患者进行了切除和活检。其中,34.2%(65/190)的患者最初被诊断为 MM,颅内浆细胞瘤是其首发表现(MM-IPFP),而 63.2%(120/190)的患者被诊断为孤立性颅内浆细胞瘤(SIP),包括 61 例髓外浆细胞瘤和 59 例孤立性骨浆细胞瘤。在 SIP 组中,22.4%(24/107)的患者在中位随访时间为 42.6 个月(范围为 1-230 个月)期间疾病进展,发展为 MM。多变量分析显示,放疗(HR,0.05;95%CI,0.00-0.87;p=0.04)而不是手术是 MM-IPFP 患者总生存的保护预后因素。SIP 进展组和非进展组之间的比较显示,Ki-67 指数存在显著差异(非进展组 vs. SIP 进展组,8.82%±7.03% vs. 16.5%±10.5%,p<0.05)。AUC 分析确定 9.0%为最佳预测 SIP 进展的截断值,曲线下面积为 0.712。

结论

这项回顾性临床分析强调了放疗而不是手术切除在改善颅内浆细胞瘤结局方面的作用。此外,Ki-67 指数被确定为预测疾病进展的有价值的标志物。这将为颅内浆细胞瘤的诊断和治疗模式提供一些来自大队列的证据。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bfcd/10922021/bdaaf5535271/CAM4-13-e7017-g001.jpg

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