Glioma-white matter tract interactions: A diffusion magnetic resonance imaging-based 3-tier classification and its clinical relevance.

IF 13.4 1区 医学 Q1 CLINICAL NEUROLOGY Neuro-oncology Pub Date : 2025-09-08 DOI:10.1093/neuonc/noaf036
Jie Hu, Hongbo Bao, Xing Liu, Shengyu Fang, Zeya Yan, Zihan Wang, Renwu Zhang, Ruiyang Wang, Tingting Pu, Chao Li, Zaixu Cui, Tao Jiang, Yinyan Wang
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Abstract

Background: This study proposed a classification system for the interaction between gliomas and white matter tracts, exploring its potential associations with clinical characteristics, tumor pathological subtypes, and patient outcomes.

Methods: Clinical data and diffusion magnetic resonance imageing (dMRI) from 360 glioma patients who underwent craniotomy were analyzed. Using automatic fiber tractography, glioma-tract relationships were categorized into 3 types: displacement, infiltration, and disruption. Double immunohistochemical staining for isocitrate dehydrogenase (IDH) and myelin basic protein was performed on neuronavigation-guided tissue samples to validate the imaging-based classifications. The clinical implications of these classifications on the extent of tumor resection, postoperative motor function, and survival outcomes were evaluated.

Results: Among the patients, 35 (9.7%) were categorized as displacement type, 283 (78.6%) as infiltration type, and 42 (11.7%) as disruption type. Disruption-type tracts were predominantly associated with IDH wild-type gliomas (87.2%), significantly higher than infiltration (28.5%) and displacement types (23.5%) (P < .001). Displacement and infiltration types were more common in IDH-mutant gliomas (P < .001). Displacement-type tracts were significantly associated with higher rates of gross tumor resection compared to infiltration types (P = .015). In corticospinal tract involved cases, displacement-type tumors demonstrated no significant postoperative motor strength changes, whereas infiltration (P < .001) and disruption types (P = .013) were highly associated with postoperative motor deficits. Histological results aligned with dMRI-based classifications.

Conclusions: This dMRI-based classification of glioma-tract interactions is significantly associated with tumor pathology, resection outcomes, functional prognosis, and survival, providing a valuable tool for personalized and precise surgical planning.

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胶质瘤-白质束相互作用:基于dmri的三层分类及其临床意义。
背景:本研究提出了胶质瘤与白质束相互作用的分类系统,探讨其与临床特征、肿瘤病理亚型和患者预后的潜在关联。方法:对360例脑胶质瘤患者行开颅手术的临床资料和弥散MRI进行分析。使用自动纤维束造影,胶质瘤与束的关系分为三种类型:移位、浸润和破坏。对神经导航引导下的组织样本进行IDH和MBP的双重免疫组化染色,以验证基于成像的分类。这些分类对肿瘤切除程度、术后运动功能和生存结果的临床意义进行了评估。结果:移位型35例(9.7%),浸润型283例(78.6%),破裂型42例(11.7%)。破坏型束主要与IDH野生型胶质瘤相关(87.2%),显著高于浸润型(28.5%)和移位型(23.5%)(P < 0.001)。移位型和浸润型在idh突变型胶质瘤中更为常见(P < 0.001)。与浸润型相比,移位型束与更高的肿瘤完全切除率显著相关(P = 0.015)。在累及皮质脊髓束的病例中,移位型肿瘤术后未表现出明显的运动强度变化,而浸润型(P < 0.001)和破坏型(P = 0.013)与术后运动功能障碍高度相关。组织学结果与基于dmri的分类一致。结论:这种基于dmri的胶质瘤-束相互作用分类与肿瘤病理、切除结果、功能预后和生存显著相关,为个性化和精确的手术计划提供了有价值的工具。
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来源期刊
Neuro-oncology
Neuro-oncology 医学-临床神经学
CiteScore
27.20
自引率
6.30%
发文量
1434
审稿时长
3-8 weeks
期刊介绍: Neuro-Oncology, the official journal of the Society for Neuro-Oncology, has been published monthly since January 2010. Affiliated with the Japan Society for Neuro-Oncology and the European Association of Neuro-Oncology, it is a global leader in the field. The journal is committed to swiftly disseminating high-quality information across all areas of neuro-oncology. It features peer-reviewed articles, reviews, symposia on various topics, abstracts from annual meetings, and updates from neuro-oncology societies worldwide.
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