Duffau Hugues
Department of Neurosurgery, Gui de Chauliac Hospital, Montpellier University Medical Center, 80 Avenue Augustin Fliche, Montpellier, 34295, France.
Team "Plasticity of Central Nervous System, Stem Cells and Low-grade Gliomas," INSERM U1191, Institute of Functional Genomics, University of Montpellier, Montpellier, France.
Curr Neurol Neurosci Rep. 2025 Jan 9;25(1):15. doi: 10.1007/s11910-024-01402-6.
In low-grade glioma (LGG), besides the patient's neurological status and tumor characteristics on neuroimaging, current treatment guidelines mainly rely on the glioma's genetics at diagnosis to define therapeutic strategy, usually starting with surgical resection. However, this snapshot in time does not take into account the antecedent period of tumor progression and its interactions with the brain before presentation. This article reviews new concepts that pertain to reconstruct the history of previous interplay between the LGG's course and adaptive changes in the connectome within which the glioma is embedded over the years preceding the diagnosis.
Microscale and macroscale parameters helpful for extrapolating backward in time are considered, both for the glioma (kinetics, migration vs. proliferation profile, metabolism with possible intratumoral heterogeneity, relationships with surrounding cerebral pathways) and for patterns of reconfiguration within and across neural networks in reaction to the LGG leading to considerable interindividual cerebral variability. Modelling these continuous variations at the time of LGG diagnosis is a prerequisite to predict recovery from treatment(s). It is important to go beyond the biology of the LGG at a given moment of its history, and instead construct a more comprehensive picture of the past and present dynamics of glioma-brain interactions, and their ongoing evolution, as a necessary stage to optimize a personalized management plan by thinking several steps ahead.
在低级别胶质瘤(LGG)中,除了患者的神经状态和神经影像学上的肿瘤特征外,当前的治疗指南主要依靠诊断时胶质瘤的遗传学来确定治疗策略,通常从手术切除开始。然而,这个时间点的情况并未考虑到肿瘤进展的前期阶段及其在出现症状之前与大脑的相互作用。本文综述了一些新概念,这些概念涉及重建在诊断前数年中LGG病程与胶质瘤所嵌入的脑连接组适应性变化之间先前相互作用的历史。
考虑了有助于进行时间回溯推断的微观和宏观参数,包括胶质瘤的参数(动力学、迁移与增殖特征、具有可能瘤内异质性的代谢、与周围脑通路的关系)以及神经网络内部和之间因LGG而导致的个体间脑内显著变异性的重构模式。在LGG诊断时对这些连续变化进行建模是预测治疗恢复情况的先决条件。重要的是,不能仅局限于LGG在其病程某一特定时刻的生物学特性,而应构建一个更全面的胶质瘤 - 脑相互作用过去和现在动态及其持续演变的图景,这是通过提前几步思考来优化个性化管理计划的必要阶段。