RELA Fusion in Supratentorial Extraventricular Ependymomas: A Morphologic, Immunohistochemical, and Molecular Study of 43 Cases

Leiming Wang, Lina Liu, Hainan Li, PeiPei Wang, Zeliang Hu, Yukui Wei, Ming Zhang, Wenjuan Wen, Zhi Li, Li Liu, Lihong Zhao, D. Lu, L. Teng
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引用次数: 12

Abstract

Supplemental Digital Content is available in the text. Supratentorial extraventricular ependymomas (STEEs) are relatively rare ependymomas, and their pathologic and genetic characteristics are still poorly understood. The aim of this study was to determine the histologic, immunohistochemical, and RELA fusion features, as well as to clarify in more detail the clinical courses of STEEs. Data from a total of 43 patients with STEEs was analyzed retrospectively. The status of RELA fusion was evaluated using fluorescence in situ hybridization. The expression levels of L1CAM, p65, cyclin D1, and p53 were assessed using immunohistochemistry. Progression-free survival and overall survival were calculated via Kaplan-Meier estimation using the log-rank test. Among all 43 STEEs, 65.1% (28/43) are positive for RELA fusion. Interestingly, almost half of the patients with RELA fusion–positive ependymomas are adults (13/28), and 89.3% (25/28) cases are anaplastic ependymomas, which suggests that RELA fusion testing is necessary in adults with STEEs. We investigated the immunohistochemical status of p65, L1CAM and CCND1 protein expression for their ability to predict RELA fusion status. RELA fusion–positive STEEs are frequently associated with expression of p65 (85.2%), L1CAM (85.2%), and CCND1 (81.5%). The accuracy of predicting RELA fusion status was much higher when the expression of p65 and L1CAM was combined, that is, when both were immunopositive. The status of RELA fusion, p53 overexpression, and extent of tumor resection are significantly associated with prognosis.
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幕上室外室管膜瘤的RELA融合:43例形态学、免疫组织化学和分子研究
补充数字内容可在文本中找到。幕上室外室管膜瘤(STEEs)是相对罕见的室管膜瘤,其病理和遗传学特征仍然知之甚少。本研究的目的是确定STEEs的组织学、免疫组织化学和RELA融合特征,并更详细地阐明STEEs的临床病程。回顾性分析43例STEEs患者的资料。采用荧光原位杂交技术评价RELA融合状态。免疫组化法检测L1CAM、p65、cyclin D1、p53的表达水平。无进展生存期和总生存期通过Kaplan-Meier估计计算,采用log-rank检验。在所有43例STEEs中,65.1%(28/43)的RELA融合阳性。有趣的是,几乎一半的RELA融合阳性室管膜瘤患者是成年人(13/28),89.3%(25/28)的病例是间变性室管膜瘤,这表明成人STEEs患者有必要进行RELA融合检测。我们研究了p65、L1CAM和CCND1蛋白表达的免疫组织化学状态,以了解它们预测RELA融合状态的能力。RELA融合阳性STEEs通常与p65(85.2%)、L1CAM(85.2%)和CCND1(81.5%)的表达相关。p65和L1CAM联合表达时,即两者均为免疫阳性时,预测RELA融合状态的准确性要高得多。RELA融合状态、p53过表达、肿瘤切除程度与预后显著相关。
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