Department of Radiation Oncology, Emory University School of Medicine, Atlanta, GA 30322, USA.
Department of Biomedical Engineering, Emory University and Georgia Institute of Technology, Atlanta, GA 30332, USA.
Tomography. 2023 Mar 9;9(2):633-646. doi: 10.3390/tomography9020051.
Radiation therapy (RT) is a critical part of definitive therapy for pediatric high-grade glioma (pHGG). RT is designed to treat residual tumor defined on conventional MRI (cMRI), though pHGG lesions may be ill-characterized on standard imaging. Spectroscopic MRI (sMRI) measures endogenous metabolite concentrations in the brain, and Choline (Cho)/N-acetylaspartate (NAA) ratio is a highly sensitive biomarker for metabolically active tumor. We provide a preliminary report of our study introducing a novel treatment approach of whole brain sMRI-guided proton therapy for pHGG. An observational cohort (c1 = 10 patients) receives standard of care RT; a therapeutic cohort (c2 = 15 patients) receives sMRI-guided proton RT. All patients undergo cMRI and sMRI, a high-resolution 3D whole-brain echo-planar spectroscopic imaging (EPSI) sequence (interpolated resolution of 12 µL) prior to RT and at several follow-up timepoints integrated into diagnostic scans. Treatment volumes are defined by cMRI for c1 and by cMRI and Cho/NAA ≥ 2x for c2. A longitudinal imaging database is used to quantify changes in lesion and metabolite volumes. Four subjects have been enrolled (c1 = 1/c2 = 3) with sMRI imaging follow-up of 4-18 months. Preliminary data suggest sMRI improves identification of pHGG infiltration based on abnormal metabolic activity, and using proton therapy to target sMRI-defined high-risk regions is safe and feasible.
放射治疗(RT)是儿童高级别神经胶质瘤(pHGG)确定性治疗的关键部分。RT 的设计目的是治疗常规 MRI(cMRI)上定义的残留肿瘤,尽管 pHGG 病变在标准成像上可能特征不明显。波谱 MRI(sMRI)测量大脑中的内源性代谢物浓度,胆碱(Cho)/N-乙酰天冬氨酸(NAA)比值是代谢活跃肿瘤的高度敏感生物标志物。我们提供了一项初步研究报告,介绍了一种新的治疗方法,即全脑 sMRI 引导质子治疗 pHGG。一个观察队列(c1=10 例)接受标准的 RT 治疗;治疗队列(c2=15 例)接受 sMRI 引导质子 RT 治疗。所有患者在 RT 前和几次随访时间点进行 cMRI 和 sMRI 检查,包括高分辨率 3D 全脑回波平面波谱成像(EPSI)序列(插值分辨率为 12 µL),并将其整合到诊断扫描中。c1 采用 cMRI 定义治疗体积,c2 采用 cMRI 和 Cho/NAA≥2x 定义治疗体积。纵向成像数据库用于定量测量病变和代谢物体积的变化。目前已经入组了 4 名受试者(c1=1/c2=3),sMRI 随访时间为 4-18 个月。初步数据表明,sMRI 可基于异常代谢活性改善 pHGG 浸润的识别,并且使用质子治疗靶向 sMRI 定义的高危区域是安全可行的。