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分子与基因分析对非典型脑膜瘤患者治疗的影响

The Impact of Molecular and Genetic Analysis on the Treatment of Patients with Atypical Meningiomas.

作者信息

Ravnik Janez, Rowbottom Hojka

机构信息

Department of Neurosurgery, University Medical Centre Maribor, 2000 Maribor, Slovenia.

出版信息

Diagnostics (Basel). 2024 Aug 15;14(16):1782. doi: 10.3390/diagnostics14161782.

DOI:10.3390/diagnostics14161782
PMID:39202270
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11353905/
Abstract

Meningiomas represent approximately 40% of all primary tumors of the central nervous system (CNS) and, based on the latest World Health Organization (WHO) guidelines, are classified into three grades and fifteen subtypes. The optimal treatment comprises gross total tumor resection. The WHO grade and the extent of tumor resection assessed by the Simpson grading system are the most important predictors of recurrence. Atypical meningiomas, a grade 2 meningioma, which represent almost a fifth of all meningiomas, have a recurrence rate of around 50%. Currently, different histopathologic, cytogenetic, and molecular genetic alterations have been associated with different meningioma phenotypes; however, the data are insufficient to enable the development of specific treatment plans. The optimal treatment, in terms of adjuvant radiotherapy and postoperative systemic therapy in atypical meningiomas, remains controversial, with inconclusive evidence in the literature and existing studies. We review the recent literature to identify studies investigating relevant atypical meningioma biomarkers and their clinical application and effects on treatment options.

摘要

脑膜瘤约占中枢神经系统(CNS)所有原发性肿瘤的40%,根据世界卫生组织(WHO)的最新指南,可分为三个级别和十五个亚型。最佳治疗方法是肿瘤全切除。WHO分级以及通过辛普森分级系统评估的肿瘤切除程度是复发的最重要预测因素。非典型脑膜瘤属于2级脑膜瘤,占所有脑膜瘤的近五分之一,复发率约为50%。目前,不同的组织病理学、细胞遗传学和分子遗传学改变与不同的脑膜瘤表型相关;然而,数据不足以制定具体的治疗方案。对于非典型脑膜瘤的辅助放疗和术后全身治疗,最佳治疗方案仍存在争议,文献和现有研究中的证据尚无定论。我们回顾了近期文献,以确定研究相关非典型脑膜瘤生物标志物及其临床应用以及对治疗选择影响的研究。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e40f/11353905/8a82467c5949/diagnostics-14-01782-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e40f/11353905/8a82467c5949/diagnostics-14-01782-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e40f/11353905/8a82467c5949/diagnostics-14-01782-g001.jpg

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Int J Mol Sci. 2024 Apr 10;25(8):4195. doi: 10.3390/ijms25084195.
2
Unveiling a Biomarker Signature of Meningioma: The Need for a Panel of Genomic, Epigenetic, Proteomic, and RNA Biomarkers to Advance Diagnosis and Prognosis.揭示脑膜瘤的生物标志物特征:需要一组基因组、表观遗传、蛋白质组和RNA生物标志物来推进诊断和预后评估。
Cancers (Basel). 2023 Nov 9;15(22):5339. doi: 10.3390/cancers15225339.
3
Atypical meningioma: Histopathological, genetic, and epigenetic features to predict recurrence risk.
非典型脑膜瘤:预测复发风险的组织病理学、遗传学和表观遗传学特征。
Histol Histopathol. 2024 Mar;39(3):293-302. doi: 10.14670/HH-18-670. Epub 2023 Oct 20.
4
Novel Advances in Treatment of Meningiomas: Prognostic and Therapeutic Implications.脑膜瘤治疗的新进展:预后及治疗意义
Cancers (Basel). 2023 Sep 12;15(18):4521. doi: 10.3390/cancers15184521.
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Intracranial meningiomas: an update of the 2021 World Health Organization classifications and review of management with a focus on radiation therapy.颅内脑膜瘤:2021年世界卫生组织分类更新及治疗综述,重点关注放射治疗
Front Oncol. 2023 Aug 22;13:1137849. doi: 10.3389/fonc.2023.1137849. eCollection 2023.
6
Atypical Intraparenchymal Meningioma with YAP1-MAML2 Fusion in a Young Adult Male: A Case Report and Mini Literature Review.青年男性脑实质内非典型脑膜瘤伴 YAP1-MAML2 融合:病例报告及文献复习
Int J Mol Sci. 2023 Aug 15;24(16):12814. doi: 10.3390/ijms241612814.
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Virchows Arch. 2023 Jul;483(1):97-104. doi: 10.1007/s00428-023-03537-2. Epub 2023 Apr 4.
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Neurooncol Adv. 2023 Jan 10;5(1):vdad004. doi: 10.1093/noajnl/vdad004. eCollection 2023 Jan-Dec.