Tumor-associated epilepsy at diagnosis in glioblastoma patients reveals an inflammatory molecular signature and is associated with better overall survival

医学 胶质母细胞瘤 癫痫 肿瘤科 总体生存率 内科学 生物标志物 胶质瘤 脑瘤 生物信息学 多中心研究 精密医学 生活质量(医疗保健) 生存分析 分子生物标志物
作者
Lilyana Dimova,Jenny Stritzelberger,Diyan Dimov,Jonas Ort,Hussam Aldin Hamou,Hans Clusmann,Oliver Schnell,HM Hamer,Florian Putz,Stefanie Corradini,Ludwig Singer,Arnd Dörfler,F Ricklefs,Richard Drexler,Matthias Simon,Dieter Henrik Heiland,Daniel Delev
出处
期刊:Neuro-oncology [Oxford University Press]
标识
DOI:10.1093/neuonc/noag134
摘要

BACKGROUND: Glioblastoma (GB) is the most aggressive primary brain tumor in adults. Tumor-associated epilepsy at diagnosis (TAE) is common, yet its prognostic significance remains unclear. METHODS: We analyzed a retrospective multicenter test cohort of 855 GB patients (Aachen, Hamburg, Bielefeld) and validated findings in a prospectively collected cohort of 344 patients (Erlangen). Survival was assessed using multivariable Cox regression, propensity score matching, and interaction modeling of TAE and extent of resection (EOR). Molecular profiling included methylation-based classification, epigenetic deconvolution, and spatial transcriptomics. RESULTS: TAE was independently associated with improved survival (HR 0.81, 95% CI 0.69-0.99, P = .036, absolute survival advantage ∼4-5 months). This effect was validated in the independent cohort (C-index 0.68 (95% CI 0.62-0.74) and persisted in propensity-matched analyses (HR 0.74, 95% CI 0.56-0.96, P = .027). Interaction modeling revealed that gross total resection (GTR) improved survival in both groups but particularly in patients with TAE (EOR interaction HR 0.69, 95% CI 0.49-0.99, P = .041). In this subgroup, partial resection provided no significant advantage over biopsy, whereas patients without seizures benefited incrementally from both partial resection and GTR. Molecular analysis demonstrated enrichment of the RTK II subtype, differentiated cell states, and an inflammatory microenvironment in glioblastoma with TAE; tumors without seizures displayed neuronal and stem-like features. Functional validation using Electrogenomics showed that glioblastoma cortical slices with increased inflammatory score exhibited synchronization of action potentials characteristic for seizure-like epileptiform activity. CONCLUSIONS: TAE at diagnosis is a favorable prognostic marker in GB, defining a biologically distinct subgroup. Seizure status modifies the prognostic effect of surgical resection, underscoring the importance of GTR particularly in patients presenting with TAE.
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