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SURG-31. SPECTROSCOPIC MRI TO GUIDE BIOPSY OF LOWER GRADE GLIOMAS

机译:SURG-31。光谱MRI引导较低级胶质瘤活检

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摘要

Primary brain tumors are serious and life-threatening; thus, accurate histopathologic diagnosis is critical for determining the proper clinical treatment regimen. Grade II/III gliomas (lower grade gliomas, or LGGs), including astrocytomas and oligodendrogliomas, are heterogeneous and potentially contain low- and high-grade areas within the same tumor. Therefore, it is critical to target biopsies to the most aggressive portion of the tumor to avoid tumor under-grading and under-treatment. While glioblastomas are typically targeted based on contrast-enhanced MRI, LGGs have little contrast enhancement to define targets for biopsy treatment guidance. Spectroscopic MRI (sMRI) is a high-resolution MRI imaging method which allows for detection of metabolic abnormalities such as choline and NAA in the entire brain without injection of a contrast agent. We have previously evaluated the relationship between sMRI Cho/NAA ratios and tumor infiltration in surgical specimens from high grade gliomas, demonstrating a strong correlation between sMRI results and glioma infiltration. We also used the location information to correlate sMRI data to genetic and histologic biomarkers (such as 1p19q, IDH, and MGMT). An IRB-approved pilot study to obtain sMRI prior to stereotactic biopsy has been done in 20 non-enhancing LGG cases. Patients with a suspected LGG diagnosis underwent sMRI at the time of their surgical planning MRI. sMRI images were then registered to the T1w-CE and T2/FLAIR images and imported into the Stealth neuronavigation system for biopsy planning. We found that all astrocytomas (regardless of grades) showed strongly elevated Cho/NAA, while the LGGs were hardly delineated on T1w and T2/FLAIR. We found that pathology-confirmed grade II oligodendroglioma do not have choline elevation; however, NAA was mildly decreased, myo-inositol was elevated, and creatine (Cr) was mildly elevated. sMRI is a useful tool to improve biopsy targeting in LGG patients by ensuring that the highest risk regions are sampled.
机译:原发性脑肿瘤是严重的,危及生命;因而,准确的组织病理学诊断为确定适当的临床治疗方案的关键。 II级/ III胶质瘤(低级级神经胶质瘤,或LGGs),包括星形细胞瘤和少突胶质细胞,是异质的和潜在包含相同的肿瘤内的低和高品位的区域。因此,关键是要针对下缓变和下处理活检的肿瘤的最积极的部分,以避免肿瘤。虽然胶质母细胞瘤通常是有针对性的基础上增强MRI,LGGs很少对比度增强定义活检处理的指导目标。分光MRI(SMRI)是一个高分辨率的MRI成像方法,其允许检测代谢异常如在整个脑胆碱和NAA的无造影剂的注入。先前我们已经评估在手术标本从高级别胶质瘤SMRI的Cho / NAA比和肿瘤浸润之间的关系,这表明SMRI结果和神经胶质瘤浸润之间的强相关性。我们还使用所述位置信息相关联SMRI数据遗传和组织学的生物标记物(如1p19q,IDH和MGMT)。一个IRB批准的试点研究,以获得SMRI前立体定位活检已在20个非增强LGG的情况下已经完成。患者疑似诊断LGG在他们的手术计划MRI的时间进行SMRI。 SMRI图像然后注册到T1W-CE和T2 / FLAIR图像和导入活检规划隐形神经导航系统。我们发现,所有星形细胞瘤(不分等级)表现出强烈升高的Cho / NAA,而LGGs都在T1W和T2 / FLAIR很难界定。我们发现,病理确诊的II级少突没有胆碱抬高;然而,NAA被轻度下降,肌醇升高,并且肌酸(CR)中的轻度升高。 SMRI是通过确保风险最高的区域进行采样,以改善患者的LGG活检目标的有用工具。

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