Price S J, Jena R, Burnet N G, Hutchinson P J, Dean A F, Peña A, Pickard J D, Carpenter T A, Gillard J H
Academic Neurosurgical Unit and Wolfson Brain Imaging Centre, Department pf Radiology, University of Cambridge and Cambridge University Hospitals NHS Foundation Trust, Addenbrooke's Hospital, Cambridge, United Kingdom.
AJNR Am J Neuroradiol. 2006 Oct;27(9):1969-74.
The efficacy of radiation therapy, the mainstay of treatment for malignant gliomas, is limited by our inability to accurately determine tumor margins. As a result, despite recent advances, the prognosis remains appalling. Because gliomas preferentially infiltrate along white matter tracks, methods that show white matter disruption should improve this delineation. In this study, results of histologic examination from samples obtained from image-guided brain biopsies were correlated with diffusion tensor images.
Twenty patients requiring image-guided biopsies for presumed gliomas were imaged preoperatively. Patients underwent image-guided biopsies with multiple biopsies taken along a single track that went into normal-appearing brain. Regions of interest were determined from the sites of the biopsies, and diffusion tensor imaging findings were compared with glioma histology.
Using diffusion tissue signatures, it was possible to differentiate gross tumor (reduction of the anisotropic component, q > 12% from contralateral region), from tumor infiltration (increase in the isotropic component, p > 10% from contralateral region). This technique has a sensitivity of 98% and specificity of 81%. T2-weighted abnormalities failed to identify the margin in half of all specimens.
Diffusion tensor imaging can better delineate the tumor margin in gliomas. Such techniques can improve the delineation of the radiation therapy target volume for gliomas and potentially can direct local therapies for tumor infiltration.
放射治疗作为恶性胶质瘤的主要治疗手段,其疗效因无法准确确定肿瘤边界而受限。因此,尽管近年来有所进展,但预后仍然很差。由于胶质瘤优先沿白质束浸润,显示白质破坏的方法应能改善这种边界的界定。在本研究中,将图像引导下脑活检获取样本的组织学检查结果与扩散张量成像结果进行了关联分析。
对20例因疑似胶质瘤而需要进行图像引导活检的患者进行术前成像。患者接受图像引导下活检,沿一条进入外观正常脑组织的单一路径进行多次活检。从活检部位确定感兴趣区域,并将扩散张量成像结果与胶质瘤组织学进行比较。
利用扩散组织特征,能够区分大体肿瘤(各向异性成分减少,与对侧区域相比q>12%)和肿瘤浸润(各向同性成分增加,与对侧区域相比p>10%)。该技术的敏感性为98%,特异性为81%。在所有标本中,半数标本的T2加权异常未能识别出边界。
扩散张量成像能够更好地界定胶质瘤的肿瘤边界。此类技术可改善胶质瘤放射治疗靶区的界定,并有可能指导针对肿瘤浸润的局部治疗。