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世界卫生组织分级和脑膜瘤的病理标志物:临床和预后作用。

WHO grade and pathological markers of meningiomas: Clinical and prognostic role.

机构信息

Department of Advanced Biomedical Sciences, Pathology Section, University of Naples "Federico II", Naples, Italy.

CEINGE Biotecnologie Avanzate scarl, via Gaetano Salvatore, 486, Naples, Italy.

出版信息

Pathol Res Pract. 2023 Mar;243:154340. doi: 10.1016/j.prp.2023.154340. Epub 2023 Jan 24.

Abstract

In recent years, WHO grading criteria have emerged as an inaccurate tool to correctly predict the risk of progression/recurrence for meningioma patients. Therefore, great efforts were made to find further prognostic factors that could predict the clinical course of meningiomas. Why morphological criteria are not able alone to correctly predict outcome in all patients? What are the biological parameters underlying a more aggressive behavior? Are there any molecular markers can be integrated in the risk assessment? Could new technologies, such as methylome profiling, contribute to provide additional tools in patients prognostic evaluation? We performed a literature review to find answers to these questions. Meningiomas have been demonstrated to be extremely heterogeneous neoplasms, also from the genetic and epigenetic standpoints. However, WHO Classification of Tumours of the central Nervous System 5th edition introduced only CDKN2A/B deletion and TERT promoter mutations as poor prognostic, grade 3 defining parameters. The different proposals of integrated grading, taking into account cytogenetic alterations and study of methylation profile, have not yet been incorporated in WHO grading criteria. Work in progress: this is the summary of current knowledge. Further studies are needed to expand the diagnostic and prognostic equipment to be integrated into clinical practice.

摘要

近年来,世界卫生组织(WHO)的分级标准已被证明是一种不准确的工具,无法正确预测脑膜瘤患者的进展/复发风险。因此,人们做出了巨大的努力来寻找进一步的预后因素,以预测脑膜瘤的临床病程。为什么形态学标准不能单独正确预测所有患者的预后?是什么生物学参数导致了更具侵袭性的行为?是否有任何分子标志物可以整合到风险评估中?新技术,如甲基化组分析,是否可以为患者的预后评估提供额外的工具?我们进行了文献回顾,以寻找这些问题的答案。脑膜瘤已被证明是具有极强异质性的肿瘤,从遗传和表观遗传的角度来看也是如此。然而,《世界卫生组织中枢神经系统肿瘤分类》第五版仅将 CDKN2A/B 缺失和 TERT 启动子突变作为预后不良的 3 级定义参数。考虑细胞遗传学改变和甲基化谱研究的综合分级的不同建议尚未被纳入世界卫生组织的分级标准。正在进行的工作:这是当前知识的总结。需要进一步的研究来扩大诊断和预后设备,将其整合到临床实践中。

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