Department of Radiation Oncology, Emory University School of Medicine, Atlanta, GA 30322, USA.
Department of Biomedical Engineering, Georgia Institute of Technology, Atlanta, GA 30322, USA.
Tomography. 2023 Feb 6;9(1):362-374. doi: 10.3390/tomography9010029.
Glioblastoma (GBM) is a fatal disease, with poor prognosis exacerbated by difficulty in assessing tumor extent with imaging. Spectroscopic MRI (sMRI) is a non-contrast imaging technique measuring endogenous metabolite levels of the brain that can serve as biomarkers for tumor extension. We completed a three-site study to assess survival benefits of GBM patients when treated with escalated radiation dose guided by metabolic abnormalities in sMRI. Escalated radiation led to complex post-treatment imaging, requiring unique approaches to discern tumor progression from radiation-related treatment effect through our quantitative imaging platform. The purpose of this study is to determine true tumor recurrence timepoints for patients in our dose-escalation multisite study using novel methodology and to report on median progression-free survival (PFS). Follow-up imaging for all 30 trial patients were collected, lesion volumes segmented and graphed, and imaging uploaded to our platform for visual interpretation. Eighteen months post-enrollment, the median PFS was 16.6 months with a median time to follow-up of 20.3 months. With this new treatment paradigm, incidence rate of tumor recurrence one year from treatment is 30% compared to 60-70% failure under standard care. Based on the delayed tumor progression and improved survival, a randomized phase II trial is under development (EAF211).
胶质母细胞瘤(GBM)是一种致命的疾病,预后不良,其肿瘤范围的评估困难加剧了这一情况。波谱磁共振成像(sMRI)是一种非对比成像技术,可测量大脑内源性代谢物水平,可作为肿瘤扩展的生物标志物。我们完成了一项三站点研究,评估了代谢异常 sMRI 指导下的强化放疗对 GBM 患者的生存获益。强化放疗导致了复杂的治疗后成像,需要通过我们的定量成像平台采用独特的方法来区分肿瘤进展和与放疗相关的治疗效果。本研究的目的是使用新方法确定我们的剂量递增多站点研究中患者的真正肿瘤复发时间点,并报告中位无进展生存期(PFS)。所有 30 名试验患者的随访成像均已收集,病变体积进行了分割和绘图,并将成像上传到我们的平台进行视觉解释。入组后 18 个月,中位 PFS 为 16.6 个月,中位随访时间为 20.3 个月。采用这种新的治疗模式,治疗后一年肿瘤复发的发生率为 30%,而标准治疗下的失败率为 60-70%。基于肿瘤进展的延迟和生存的改善,一项随机的 II 期试验正在开发中(EAF211)。