Rauch Philip, Gmeiner Matthias, Aichholzer Martin, Sterrer Matthias, Wagner Helga, Katletz Stefan, Serra Carlo, Böhm Petra, Sonnberger Michael, Stroh Nico, Aspalter Stefan, Aufschnaiter-Hiessböck Kathrin, Rossmann Tobias, Ruiz-Navarro Francisco, Gollwitzer Maria, Leibetseder Annette, Pichler Josef, Thomae Wolfgang, Kleiser Raimund, Gruber Andreas, Stefanits Harald
Department of Neurosurgery, Kepler University Hospital and Johannes Kepler University Linz, Linz 4040, Austria.
Clinical Research Institute for Neuroscience, Faculty of Medicine, Johannes Kepler University Linz, Linz 4020, Austria.
Brain Commun. 2025 Apr 19;7(3):fcaf157. doi: 10.1093/braincomms/fcaf157. eCollection 2025.
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 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.
低级别胶质瘤是浸润性脑肿瘤,因其侵袭性本质可导致显著的神经功能缺损。目前普遍认为,低级别胶质瘤主要沿白质束扩散,但缺乏支持这一概念的定量证据。阐明其真正的生长模式对于优化治疗策略至关重要。我们对43例未经治疗的单脑叶世界卫生组织2级或3级胶质瘤患者的纵向队列中的肿瘤生长模式进行了定量分析,根据其在新皮质、中皮质和旧皮质内的解剖位置进行分层。连续的磁共振成像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。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一致性。定量分析表明,低级别胶质瘤并非主要沿白质束扩展。相反,就其起源的拓扑结构而言,它们局限于特定的解剖边界内。角度测量和热图分析表明,肿瘤生长指向脑室下区,并可能遵循各自的放射状单元。在不同解剖区域的这些一致观察结果挑战了传统的胶质瘤进展模型,表明早期胶质瘤扩展受个体发生因素密切支配。总之,本研究提供了首个定量证据,表明表型低级别胶质瘤并非主要遵循白质束,而是可能受个体发生机制影响。这些见解需要重新评估现有的胶质瘤进展模型,并强调将发育方面纳入治疗计划以改善患者预后的重要性。