Bhutada Abhishek S, Adhikari Srijan, Cuoco Joshua A, Hoggarth Austin R, Patel Vaibhav M, Olasunkanmi Adeolu L
Department of Neurosurgery, Virginia Tech Carilion School of Medicine, Roanoke, VA, USA.
Department of Neurosurgery, Carilion Clinic, Roanoke, VA, USA.
Global Spine J. 2025 May;15(4):1905-1913. doi: 10.1177/21925682241270101. Epub 2024 Nov 1.
Study DesignRetrospective Study.ObjectiveMyxopapillary ependymomas (MPEs) are a unique subgroup of spinal ependymomas originating from the filum terminale's ependymal glia. The 2021 WHO classification reclassified all MPEs as grade 2, recognizing their higher recurrence risk. Due to their rarity, our objective with this study is to understand MPEs' clinical course and optimal management through a large retrospective cohort analysis.MethodsFrom the years 2000 to 2020, patients with MPEs were identified from the Surveillance, Epidemiology, and End Results (SEER) database. Univariate and multivariable Cox proportional hazard models were run to identify variables that had a significant impact on the primary endpoint of overall survival (OS). A predictive nomogram was built to predict 5-year and 10-year survival probability.ResultsThis retrospective cohort includes 1373 patients. Patients 65 years or older at diagnosis had a poorer OS ( < 0.001). Most patients received subtotal resection. Only 320 patients (23%) received gross total resection (GTR). Patients that received GTR had the best OS when compared against all other modalities of treatment ( < 0.05). Receiving radiotherapy did not affect OS in patients with MPE ( = 0.2). Nomogram includes patient age and treatment modalities, demonstrating acceptable accuracy in estimating the survival probability at 5-year and 10-year intervals, with a C-index of 0.80 (95% CI of 0.71 to 0.90).ConclusionThis study highlights the survival benefit of GTR in the treatment of patients with MPE. The role of adjuvant radiotherapy remains unclear as it did not seem to improve OS. The nomogram stratifies the risk of survival in patients with MPE based on age and treatment modality.
研究设计
回顾性研究。
目的
黏液乳头型室管膜瘤(MPE)是脊髓室管膜瘤的一个独特亚组,起源于终丝的室管膜胶质细胞。2021年世界卫生组织(WHO)分类将所有MPE重新分类为2级,认识到它们有更高的复发风险。由于其罕见性,我们本研究的目的是通过大型回顾性队列分析了解MPE的临床病程和最佳治疗方法。
方法
从2000年到2020年,从监测、流行病学和最终结果(SEER)数据库中识别出患有MPE的患者。运行单变量和多变量Cox比例风险模型,以确定对总生存期(OS)这一主要终点有显著影响的变量。构建一个预测列线图来预测5年和10年生存概率。
结果
这个回顾性队列包括1373名患者。诊断时年龄在65岁及以上的患者OS较差(<0.001)。大多数患者接受了次全切除。只有320名患者(23%)接受了全切除(GTR)。与所有其他治疗方式相比,接受GTR的患者OS最佳(<0.05)。接受放疗对MPE患者的OS没有影响(=0.2)。列线图包括患者年龄和治疗方式,在估计5年和10年间隔的生存概率时显示出可接受的准确性,C指数为0.80(95%CI为0.71至0.90)。
结论
本研究强调了GTR在MPE患者治疗中的生存获益。辅助放疗的作用仍不明确,因为它似乎并未改善OS。列线图根据年龄和治疗方式对MPE患者的生存风险进行分层。