Kim Michelle M, Parmar Hemant A, Aryal Madhava P, Mayo Charles S, Balter James M, Lawrence Theodore S, Cao Yue
Departments of Radiation Oncology and.
Radiology, University of Michigan, Ann Arbor, MI.
Tomography. 2019 Mar;5(1):118-126. doi: 10.18383/j.tom.2018.00035.
Quantitative mapping of hyperperfused and hypercellular regions of glioblastoma has been proposed to improve definition of tumor regions at risk for local recurrence following conventional radiation therapy. As the processing of the multiparametric dynamic contrast-enhanced (DCE-) and diffusion-weighted (DW-) magnetic resonance imaging (MRI) data for delineation of these subvolumes requires additional steps that go beyond the standard practices of target definition, we sought to devise a workflow to support the timely planning and treatment of patients. A phase II study implementing a multiparametric imaging biomarker for tumor hyperperfusion and hypercellularity consisting of DCE-MRI and high b-value DW-MRI to guide intensified (75 Gy/30 fractions) radiation therapy (RT) in patients with newly diagnosed glioblastoma was launched. In this report, the workflow and the initial imaging outcomes of the first 12 patients are described. Among all the first 12 patients, treatment was initiated within 6 weeks of surgery and within 2 weeks of simulation. On average, the combined hypercellular volume and high cerebral blood volume/tumor perfusion volume were 1.8 times smaller than the T1 gadolinium abnormality and 10 times smaller than the FLAIR abnormality. Hypercellular volume and high cerebral blood volume/tumor perfusion volume each identified largely distinct regions and showed 57% overlap with the enhancing abnormality, and minimal-to-no extension outside of the FLAIR. These results show the feasibility of implementing a workflow for multiparametric magnetic resonance-guided radiation therapy into clinical trials with a coordinated multidisciplinary team, and the unique and complementary tumor subregions identified by the combination of high b-value DW-MRI and DCE-MRI.
已有人提出对胶质母细胞瘤的高灌注和高细胞区域进行定量映射,以更好地界定常规放射治疗后有局部复发风险的肿瘤区域。由于处理多参数动态对比增强(DCE-)和扩散加权(DW-)磁共振成像(MRI)数据以描绘这些子体积需要超出靶区定义标准做法的额外步骤,我们试图设计一种工作流程以支持患者的及时规划和治疗。开展了一项II期研究,该研究采用由DCE-MRI和高b值DW-MRI组成的用于肿瘤高灌注和高细胞性的多参数成像生物标志物,以指导新诊断胶质母细胞瘤患者的强化(75 Gy/30次分割)放射治疗(RT)。在本报告中,描述了前12例患者的工作流程和初始成像结果。在前12例患者中,均在手术6周内且模拟2周内开始治疗。平均而言,高细胞体积与高脑血容量/肿瘤灌注体积之和比T1钆异常小1.8倍,比液体衰减反转恢复(FLAIR)异常小10倍。高细胞体积和高脑血容量/肿瘤灌注体积各自识别出的区域在很大程度上不同,与强化异常区域有57%的重叠,且在FLAIR之外的延伸最小至无延伸。这些结果表明,在多学科团队协作下,将多参数磁共振引导放射治疗工作流程应用于临床试验是可行的,并且高b值DW-MRI和DCE-MRI联合识别出了独特且互补的肿瘤子区域。