Tobochnik Steven, Regan Michael S, Dorotan Maria K C, Reich Dustine, Lapinskas Emily, Hossain Md Amin, Stopka Sylwia, Santagata Sandro, Murphy Melissa M, Arnaout Omar, Bi Wenya Linda, Antonio Chiocca E, Golby Alexandra J, Mooney Michael A, Smith Timothy R, Ligon Keith L, Wen Patrick Y, Agar Nathalie Y R, Lee Jong Woo
Department of Neurology, Brigham and Women's Hospital, Boston, MA, USA.
Department of Neurology, VA Boston Healthcare System, Boston, MA, USA.
medRxiv. 2024 Apr 18:2024.04.11.24305666. doi: 10.1101/2024.04.11.24305666.
Glutamatergic neuron-glioma synaptogenesis and peritumoral hyperexcitability promote glioma growth in a positive feedback loop. The objective of this study was to evaluate the feasibility and estimated effect sizes of the AMPA-R antagonist, perampanel, on intraoperative electrophysiologic hyperexcitability and clinical outcomes.
An open-label trial was performed comparing perampanel to standard of care (SOC) in patients undergoing resection of newly-diagnosed radiologic high-grade glioma. Perampanel was administered as a pre-operative loading dose followed by maintenance therapy until progressive disease or up to 12-months. SOC treatment involved levetiracetam for 7-days or as clinically indicated. The primary outcome of hyperexcitability was defined by intra-operative electrocorticography high frequency oscillation (HFO) rates. Seizure-freedom and overall survival (OS) were estimated by the Kaplan-Meier method. Tissue concentrations of perampanel, levetiracetam, and metabolites were measured by mass spectrometry.
HFO rates were similar between perampanel-treated and SOC cohorts. The trial was terminated early after interim analysis for futility, and outcomes assessed in 11 patients (7 perampanel-treated, 4 SOC). Over a median 281 days of post-enrollment follow-up, 27% of patients had seizures, including 14% treated with perampanel and 50% treated with SOC. OS in perampanel-treated patients was similar to a glioblastoma reference cohort (p=0.81). Glutamate concentrations in surface biopsies were positively correlated with HFO rates in adjacent electrode contacts and were not significantly associated with treatment assignment or drug concentrations.
A peri-operative loading regimen of perampanel was safe and well-tolerated, with similar peritumoral hyperexcitability as in levetiracetam-treated patients. Maintenance anti-glutamatergic therapy was not observed to impact survival outcomes.
谷氨酸能神经元-胶质瘤突触形成和瘤周兴奋性过高以正反馈回路促进胶质瘤生长。本研究的目的是评估AMPA-R拮抗剂吡仑帕奈对术中电生理兴奋性过高和临床结局的可行性及估计效应大小。
在新诊断的影像学高级别胶质瘤切除患者中进行了一项开放标签试验,将吡仑帕奈与标准治疗(SOC)进行比较。吡仑帕奈作为术前负荷剂量给药,随后进行维持治疗,直至疾病进展或长达12个月。SOC治疗包括左乙拉西坦治疗7天或根据临床指征使用。兴奋性过高的主要结局由术中皮层脑电图高频振荡(HFO)率定义。无癫痫发作和总生存期(OS)通过Kaplan-Meier方法估计。通过质谱法测量吡仑帕奈、左乙拉西坦及其代谢物的组织浓度。
吡仑帕奈治疗组和SOC队列的HFO率相似。在中期分析因无效而提前终止试验,对11例患者(7例接受吡仑帕奈治疗,4例接受SOC治疗)的结局进行了评估。在入组后中位281天的随访中,27%的患者发生癫痫,其中接受吡仑帕奈治疗的患者为14%,接受SOC治疗的患者为50%。接受吡仑帕奈治疗的患者的OS与胶质母细胞瘤参考队列相似(p = 0.81)。表面活检中的谷氨酸浓度与相邻电极触点的HFO率呈正相关,与治疗分配或药物浓度无显著关联。
吡仑帕奈的围手术期负荷方案安全且耐受性良好,瘤周兴奋性过高情况与左乙拉西坦治疗的患者相似。未观察到维持性抗谷氨酸能治疗对生存结局有影响。