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2016年世界卫生组织II-III级胶质瘤亚型之间的影像学差异:一项系统评价和荟萃分析

Radiological differences between subtypes of WHO 2016 grade II-III gliomas: a systematic review and meta-analysis.

作者信息

van Lent Djuno I, van Baarsen Kirsten M, Snijders Tom J, Robe Pierre A J T

机构信息

Department of Neurology and Neurosurgery, Brain Center Rudolf Magnus, University Medical Center Utrecht, Utrecht, The Netherlands.

Department of Neuro-Oncology, Princess Maxima Center for Pediatric Oncology, Utrecht, The Netherlands.

出版信息

Neurooncol Adv. 2020 Apr 4;2(1):vdaa044. doi: 10.1093/noajnl/vdaa044. eCollection 2020 Jan-Dec.

Abstract

BACKGROUND

Isocitrate dehydrogenase (IDH) mutation and 1p/19q-codeletion are oncogenetic alterations with a positive prognostic value for diffuse gliomas, especially grade II and III. Some studies have suggested differences in biological behavior as reflected by radiological characteristics. In this paper, the literature regarding radiological characteristics in grade II and III glioma subtypes was systematically evaluated and a meta-analysis was performed.

METHODS

Studies that addressed the relationship between conventional radiological characteristics and IDH mutations and/or 1p/19q-codeletions in newly diagnosed, grade II and III gliomas of adult patients were included. The "3-group analysis" compared radiological characteristics between the WHO 2016 glioma subtypes (IDH-mutant astrocytoma, IDH-wildtype astrocytoma, and oligodendroglioma), and the "2-group analysis" compared radiological characteristics between 1p/19q-codeleted gliomas and 1p/19q-intact gliomas.

RESULTS

Fourteen studies (3-group analysis: 670 cases, 2-group analysis: 1042 cases) were included. IDH-mutated astrocytomas showed more often sharp borders and less frequently contrast enhancement compared to IDH-wildtype astrocytomas. 1p/19q-codeleted gliomas had less frequently sharp borders, but showed a heterogeneous aspect, calcification, cysts, and edema more frequently. For the 1p/19q-codeleted gliomas, a sensitivity of 96% was found for heterogeneity and a specificity of 88.1% for calcification.

CONCLUSIONS

Significant differences in conventional radiological characteristics exist between the WHO 2016 glioma subtypes, which may reflect differences in biological behavior. However, the diagnostic value of the independent radiological characteristics is insufficient to reliably predict the molecular genetic subtype.

摘要

背景

异柠檬酸脱氢酶(IDH)突变和1p/19q共缺失是弥漫性胶质瘤的致癌性改变,对II级和III级胶质瘤具有积极的预后价值。一些研究表明,生物学行为存在差异,这在放射学特征中有所体现。本文系统评估了关于II级和III级胶质瘤亚型放射学特征的文献,并进行了荟萃分析。

方法

纳入研究新诊断的成年患者II级和III级胶质瘤中常规放射学特征与IDH突变和/或1p/19q共缺失之间关系的研究。“三组分析”比较了2016年世界卫生组织(WHO)胶质瘤亚型(IDH突变型星形细胞瘤、IDH野生型星形细胞瘤和少突胶质细胞瘤)之间的放射学特征,“两组分析”比较了1p/19q共缺失的胶质瘤和1p/19q完整的胶质瘤之间的放射学特征。

结果

纳入了14项研究(三组分析:670例,两组分析:1042例)。与IDH野生型星形细胞瘤相比,IDH突变型星形细胞瘤边界更常清晰,强化更少见。1p/19q共缺失的胶质瘤边界清晰的情况较少见,但更常表现为不均匀、钙化、囊肿和水肿。对于1p/19q共缺失的胶质瘤,不均匀性的敏感性为96%,钙化的特异性为88.1%。

结论

2016年WHO胶质瘤亚型之间在常规放射学特征上存在显著差异,这可能反映了生物学行为的差异。然而,独立放射学特征的诊断价值不足以可靠地预测分子遗传亚型。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c7fd/7236393/47a328699955/vdaa044f0002.jpg

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