论文标题

肿瘤在治疗前的MRI位置可以预测假产生的可能性与胶质母细胞瘤中肿瘤复发的可能性吗?可行性研究

Can tumor location on pre-treatment MRI predict likelihood of pseudo-progression versus tumor recurrence in Glioblastoma? A feasibility study

论文作者

Ismail, Marwa, Hill, Virginia, Statsevych, Volodymyr, Mason, Evan, Correa, Ramon, Prasanna, Prateek, Singh, Gagandeep, Bera, Kaustav, Thawani, Rajat, Madabhushi, Anant, Ahluwalia, Manmeet, Tiwari, Pallavi

论文摘要

胶质母细胞瘤(GBM)管理中的一个重大挑战是鉴定伪产生(PSP),良性辐射诱导的效果,肿瘤复发,对常规处理后常规成像。先前的研究已将肿瘤叶的存在和侧向与GBM结果联系起来,这表明GBM的疾病病因和进展可能受到肿瘤位置的影响。因此,在这项可行性研究中,我们试图调查以下问题:肿瘤的位置是否可以在治疗中获得的MRI提供有关患者发生假产生可能性与肿瘤复发的可能性的早期线索?在这项研究中,分析了74例治疗前胶质母细胞瘤MRI扫描,并分析了PSP(33)和肿瘤复发(41)。首先,专家对T2W/FLAIR上的GD-T1W MRI和体内过度强度的增强病变进行了分割,然后注册到大脑地图集。使用来自两种表型的患者,我们通过量化增强病变和肿瘤周日过度强度的发生频率来构建两个图形,这是通过平均整个人群中的体素强度来构建的。然后对差异参与进行分析,以计算整个地带之间的体素显着差异(p值<0.05)。最终将具有统计学意义的簇映射到结构地图集,以提供其位置的解剖定位。我们的结果表明,肿瘤复发的患者在顶叶中表现出其初始肿瘤的突出,而PSP患者在额叶和颞叶,岛状和pe骨中显示了初始肿瘤的多焦点分布。这些初步结果表明,对大脑某些解剖区域的治疗前病变的横向化可能允许提供早期的提示,以评估MRI扫描中肿瘤复发的假期发生的可能性。

A significant challenge in Glioblastoma (GBM) management is identifying pseudo-progression (PsP), a benign radiation-induced effect, from tumor recurrence, on routine imaging following conventional treatment. Previous studies have linked tumor lobar presence and laterality to GBM outcomes, suggesting that disease etiology and progression in GBM may be impacted by tumor location. Hence, in this feasibility study, we seek to investigate the following question: Can tumor location on treatment-naïve MRI provide early cues regarding likelihood of a patient developing pseudo-progression versus tumor recurrence? In this study, 74 pre-treatment Glioblastoma MRI scans with PsP (33) and tumor recurrence (41) were analyzed. First, enhancing lesion on Gd-T1w MRI and peri-lesional hyperintensities on T2w/FLAIR were segmented by experts and then registered to a brain atlas. Using patients from the two phenotypes, we construct two atlases by quantifying frequency of occurrence of enhancing lesion and peri-lesion hyperintensities, by averaging voxel intensities across the population. Analysis of differential involvement was then performed to compute voxel-wise significant differences (p-value<0.05) across the atlases. Statistically significant clusters were finally mapped to a structural atlas to provide anatomic localization of their location. Our results demonstrate that patients with tumor recurrence showed prominence of their initial tumor in the parietal lobe, while patients with PsP showed a multi-focal distribution of the initial tumor in the frontal and temporal lobes, insula, and putamen. These preliminary results suggest that lateralization of pre-treatment lesions towards certain anatomical areas of the brain may allow to provide early cues regarding assessing likelihood of occurrence of pseudo-progression from tumor recurrence on MRI scans.

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