应用VASARI特征鉴别儿童幕上室管膜瘤和高级别胶质瘤。

Carmen R Cerron-Vela, Fabrício Guimarães Gonçalves, Luis Octavio Tierradentro-García, Angela N Viaene, Aashim Bhatia, Arastoo Vossough
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引用次数: 0

摘要

背景与目的:幕上室管膜瘤(sEPN)和幕上高级别胶质瘤(sHGG)是罕见的儿童肿瘤,具有重叠的影像学特征,术前鉴别具有挑战性。准确的区分对于确定适当的处理,指导手术决策至关重要。视觉上可访问的伦勃朗图像(VASARI)特征集是一个标准化的基于mri的系统,用于描述胶质瘤的成像特征。VASARI已被证明是可获得的,可重复的,并且在临床上有助于表征肿瘤形态。我们假设结合影像学特征可以区分这两种肿瘤类型。我们评估了一个患有sEPN和sHGG的儿科队列,以确定不同的影像学特征,考虑人口统计学和影像学因素。这种方法旨在提高诊断的准确性和改善个性化的治疗计划。材料和方法:本回顾性研究纳入2000年至2023年间年龄< 21岁,组织学或分子证实为sEPN或sHGG的患者。我们评估了36个影像学特征(54个包括亚分类),结合VASARI集和其他肿瘤特征参数。单因素分析评估了人口统计学和影像学特征与肿瘤类型之间的关系,然后进行了多因素logistic回归。最后,采用正则化和变量选择的广义二项回归方法,构建了用于临床的关键特征的简化简约模型。结果:纳入45例患者,其中sepn 26例,sHGGs 19例。各组间性别分布相似(sEPN为61.5%,sHGG为78.9%,p=0.18)。结论:虽然sEPN和sHGG具有重叠的影像学特征,但结合16个常规MRI特征可以充分区分两者。两种特征的较小子集(定义为非增强边缘的钙化或定义为增强边缘和非增强边缘的钙化)也提供了较高的诊断准确性。这些特征组合改善了分化,可能支持更明智的治疗决策,可能导致更好的患者预后。缩写:sEPN =幕上室管膜瘤;sHGG =幕上高级胶质瘤;VASARI =视觉上可访问的伦勃朗图像功能集。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Imaging Differentiation of Supratentorial Ependymoma and High-grade Glioma in Children using VASARI Features.

Background and purpose: Supratentorial ependymomas (sEPN) and supratentorial high-grade gliomas (sHGG) are rare pediatric tumors with overlapping imaging features, making preoperative differentiation challenging. Accurate distinction is crucial for determining the appropriate management, guiding surgical decisions. The Visually Accessible Rembrandt Images (VASARI) feature set is a standardized MRI-based system for describing imaging characteristics of gliomas. VASARI has proven accessible, reproducible, and clinically helpful in characterizing tumor morphology. We hypothesize that a combination of imaging features can distinguish between these two tumor types. We evaluated a pediatric cohort with sEPN and sHGG to identify distinguishing imaging features, considering demographic and imaging factors. This approach aims to enhance diagnostic accuracy and improve individualized treatment planning.

Materials and methods: This retrospective study enrolled patients < 21 years old, with a histologically or molecularly confirmed sEPN or sHGG between 2000 and 2023. We evaluated 36 imaging features (54 including subcategories), incorporating VASARI set and additional tumor characterization parameters. Univariate analysis assessed relationships between demographic and imaging features and tumor type, followed by multivariate logistic regression. Finally, generalized binomial regression with regularization and variable selection was used to construct simplified parsimonious models of key distinguishing features for clinical use.

Results: 45 patients were included, 26 sEPNs and 19 sHGGs. Sex distribution was similar between groups (61.5% female in sEPN and 78.9% in sHGG, p=0.18). By univariable analysis 16 imaging features differed significantly between tumors (p<0.05), including proportion of enhancing/non-enhancing components, calcifications, T1WI/FLAIR ratio, T2WI signal, calvarial remodeling, and involvement of specific brain regions. Multivariate analysis incorporating these features achieved 100% accuracy in differentiating the tumors (AUC=1). A smaller parsimonious model that combined presence of calcifications and non-enhancing margin definition, accurately distinguished the tumors (AUC=0.98). Alternatively, using enhancing and non-enhancing margin definitions also achieved high accuracy (AUC=0.95).

Conclusions: Although sEPN and sHGG share overlapping imaging characteristics, a combination of 16 routine MRI features can fully differentiate them. Smaller subsets of two features (calcifications with definition of non-enhancing margins or the definitions of both enhancing and non-enhancing margins), also provide high diagnostic accuracy. These feature combinations improve differentiation and may support more informed treatment decisions, potentially leading to better patient outcomes.

Abbreviations: sEPN = Supratentorial ependymomas; sHGG = supratentorial high-grade gliomas; VASARI = The Visually Accessible Rembrandt Images feature set.

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