低级别胶质瘤不沿白质束生长:来自定量成像的证据。

IF 4.1 Q1 CLINICAL NEUROLOGY
Brain communications Pub Date : 2025-04-19 eCollection Date: 2025-01-01 DOI:10.1093/braincomms/fcaf157
Philip Rauch, Matthias Gmeiner, Martin Aichholzer, Matthias Sterrer, Helga Wagner, Stefan Katletz, Carlo Serra, Petra Böhm, Michael Sonnberger, Nico Stroh, Stefan Aspalter, Kathrin Aufschnaiter-Hiessböck, Tobias Rossmann, Francisco Ruiz-Navarro, Maria Gollwitzer, Annette Leibetseder, Josef Pichler, Wolfgang Thomae, Raimund Kleiser, Andreas Gruber, Harald Stefanits
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引用次数: 0

摘要

低级别胶质瘤是一种浸润性脑肿瘤,由于其侵袭性,可导致严重的神经功能障碍。普遍认为,低级别胶质瘤主要沿白质束扩散,但缺乏定量的体内证据支持这一概念。明确其真实的生长模式对于优化治疗策略至关重要。我们对43例未经治疗的世界卫生组织2级或3级单一胶质瘤患者进行了肿瘤生长模式的纵向队列定量分析,并根据其在新皮层、中皮层和异位皮层的解剖位置进行了分层。连续MRI扫描用于生成矢量变形场,提供肿瘤随时间演变的详细三维表示。将这些矢量变形场与扩散张量成像数据进行比较,以评估肿瘤生长与白质通路的对齐。定量分析显示,低级别胶质瘤并不主要沿白质束扩张。相反,它们仍然被限制在特定的解剖边界内,就它们的起源拓扑结构而言。角度测量和热图分析表明肿瘤生长指向室下区,并可能遵循各自的径向单位。这些在不同解剖区域的一致观察结果挑战了传统的胶质瘤进展模型,表明早期胶质瘤的扩张与个体发生因素密切相关。总之,这项研究提供了第一个定量证据,表明表型低级别胶质瘤并不主要遵循白质束,而是可能受到个体发生机制的影响。这些见解需要对现有的胶质瘤进展模型进行重新评估,并强调将发育方面纳入治疗计划以提高患者预后的重要性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Low-grade gliomas do not grow along white matter tracts: evidence from quantitative imaging.

Low-grade gliomas are infiltrative brain tumors that can lead to significant neurological deficits due to their invasive nature. The prevailing belief is that low-grade gliomas primarily disseminate along white matter tracts, but quantitative in vivo evidence supporting this concept is lacking. Clarifying their true growth patterns is essential for optimizing therapeutic strategies. We conducted a quantitative analysis of tumor growth patterns in a longitudinal cohort of 43 untreated patients with unigyral World Health Organization grade 2 or 3 gliomas, stratified by their anatomical locations within the neocortex, mesocortex and allocortex. Serial MRI scans were used to generate vector deformation fields, providing detailed three-dimensional representations of tumor evolution over time. These vector deformation fields were compared with diffusion tensor imaging data to assess the alignment of tumor growth with white matter pathways. Quantitative analysis revealed that low-grade gliomas do not predominantly expand along white matter tracts. Instead, they remain confined within specific anatomical boundaries, in respect to their topology of origin. Angular measurements and heat map analysis indicated that tumor growth is directed towards the subventricular zone and may follow their respective radial units. These consistent observations across different anatomical regions challenge the traditional model of glioma progression, suggesting that early-stage glioma expansion is closely governed by ontogenetic factors. In conclusion, this study provides the first quantitative evidence that phenotypical low-grade gliomas do not primarily follow white matter tracts but may instead be influenced by ontogenetic mechanisms. These insights necessitate a re-evaluation of existing models of glioma progression and underscore the importance of incorporating developmental aspects into treatment planning to enhance patient outcomes.

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CiteScore
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