Division of MR Research, Department of Radiology, Johns Hopkins University, Baltimore, Maryland (X.H., M.W., Y.F., B.M., S.W., J.Z.); Cancer Center, Union Hospital, Tongji Medical College, Huazhong University of Science and Technology, Wuhan, Hubei, China (X.H., L.L.); Department of Radiation Oncology, Johns Hopkins University, Baltimore, Maryland (K.D., J.W.); Department of Neurology, Kennedy Krieger Institute, Baltimore, Maryland (B.L., J.L.); Department of Neurosurgery, Johns Hopkins University, Baltimore, Maryland (B.T., A.M.); Department of Neurology, Johns Hopkins University, Baltimore, Maryland (J.L.); F.M. Kirby Research Center for Functional Brain Imaging, Kennedy Krieger Institute, Baltimore, Maryland (J.Z.).
Neuro Oncol. 2014 Jun;16(6):856-67. doi: 10.1093/neuonc/not245. Epub 2013 Dec 22.
The inability of structural MRI to accurately measure tumor response to therapy complicates care management for patients with gliomas. The purpose of this study was to assess the potential of several noninvasive functional and molecular MRI biomarkers for the assessment of glioma response to radiotherapy.
Fourteen U87 tumor-bearing rats were irradiated using a small-animal radiation research platform (40 or 20 Gy), and 6 rats were used as controls. MRI was performed on a 4.7 T animal scanner, preradiation treatment, as well as at 3, 6, 9, and 14 days postradiation. Image features of the tumors, as well as tumor volumes and animal survival, were quantitatively compared.
Structural MRI showed that all irradiated tumors still grew in size during the initial days postradiation. The apparent diffusion coefficient (ADC) values of tumors increased significantly postradiation (40 and 20 Gy), except at day 3 postradiation, compared with preradiation. The tumor blood flow decreased significantly postradiation (40 and 20 Gy), but the relative blood flow (tumor vs contralateral) did not show a significant change at most time points postradiation. The amide proton transfer weighted (APTw) signals of the tumor decreased significantly at all time points postradiation (40 Gy), and also at day 9 postradiation (20 Gy). The blood flow and APTw maps demonstrated tumor features that were similar to those seen on gadolinium-enhanced T1-weighted images.
Tumor ADC, blood flow, and APTw were all useful imaging biomarkers by which to predict glioma response to radiotherapy. The APTw signal was most promising for early response assessment in this model.
结构性磁共振成像无法准确测量肿瘤对治疗的反应,这使得胶质瘤患者的治疗管理变得复杂。本研究旨在评估几种非侵入性功能和分子磁共振成像生物标志物在评估胶质瘤对放射治疗反应中的潜力。
将 14 只 U87 肿瘤荷瘤大鼠用小动物放射研究平台(40 或 20Gy)进行照射,6 只大鼠作为对照。在 4.7T 动物扫描仪上进行 MRI 检查,在照射前,以及照射后 3、6、9 和 14 天进行检查。对肿瘤的图像特征以及肿瘤体积和动物存活率进行定量比较。
结构性 MRI 显示,所有照射后的肿瘤在照射后最初几天仍在生长。肿瘤的表观扩散系数(ADC)值在照射后(40 和 20Gy)显著增加,除了照射后第 3 天。肿瘤血流量在照射后(40 和 20Gy)显著降低,但相对血流量(肿瘤与对侧)在大多数照射后时间点没有显著变化。肿瘤酰胺质子转移加权(APTw)信号在照射后所有时间点(40Gy)均显著降低,在照射后第 9 天(20Gy)也显著降低。血流和 APTw 图谱显示肿瘤特征与钆增强 T1 加权图像所见相似。
肿瘤 ADC、血流和 APTw 都是预测胶质瘤对放射治疗反应的有用成像生物标志物。在该模型中,APTw 信号最有希望用于早期反应评估。