Ahmanson Translational Imaging Division, Department of Molecular and Medical Pharmacology, David Geffen School of Medicine at University of California Los Angeles, Los Angeles,California (K.H., J.C., K.P., M.R.B., M.E.P., W.C.); Department of Neurology, David Geffen School of Medicine at University of California Los Angeles,Los Angeles,California (T.C., A.L.); Department of Nuclear Medicine, Universitätsklinikum Würzburg, Würzburg, Germany (K.H., A.K.B.).
Neuro Oncol. 2014 Apr;16(4):603-9. doi: 10.1093/neuonc/not166. Epub 2013 Dec 4.
Amino acid transport imaging with 18F-FDOPA PET is increasingly used for detection of glioblastoma recurrence. However, a standardized image interpretation for 18F-FDOPA brain PET studies has not yet been established. This study compares visual and semiquantitative analysis parameters for detection of tumor recurrence and correlates them with progression-free survival (PFS).
One-hundred ten patients (72 male:38 female) with suspected tumor recurrence who underwent 18F-FDOPA PET imaging were studied. PET scans were analyzed visually (5-point scale) and semiquantitatively (lesion-to-striatum- and lesion- to-normal-brain-tissue ratios using both SUV(mean) and SUV(max)). Accuracies for recurrence detection were calculated using histopathology and clinical follow-up for validation. Receiving operator characteristic and Kaplan-Meier survival analysis were performed to derive imaging-based prediction of PFS and overall survival (OS).
Accuracies for detection of glioblastoma recurrence were similar for visual (82%) and semiquantitative (range, 77%-82%) analysis. Both visual and semiquantitative indices were significant predictors of PFS, with mean lesion-to normal brain tissue ratios providing the best discriminator (mean survival, 39.4 vs 9.3 months; P < .001). None of the investigated parameters was predictive for OS.
Both visual and semiquantitative indices detected glioblastoma recurrence with high accuracy and were predictive for PFS. Lesion-to-normal-tissue ratios were the best discriminators of PFS; however, none of the investigated parameters predicted OS. These retrospectively established analysis parameters need to be confirmed prospectively.
18F-FDOPA PET 氨基酸转运成像越来越多地用于检测胶质母细胞瘤的复发。然而,尚未建立 18F-FDOPA 脑 PET 研究的标准化图像解读。本研究比较了视觉和半定量分析参数在检测肿瘤复发中的应用,并将其与无进展生存期(PFS)相关联。
对 110 例疑似肿瘤复发的患者(72 例男性:38 例女性)进行了 18F-FDOPA PET 成像研究。PET 扫描通过视觉(5 分制)和半定量(使用 SUV(均值)和 SUV(最大值)的病灶与纹状体和病灶与正常脑组织比值)进行分析。使用组织病理学和临床随访对准确性进行验证,以计算复发检测的准确性。进行接受者操作特征和 Kaplan-Meier 生存分析,以获得基于成像的 PFS 和总生存期(OS)预测。
视觉(82%)和半定量(范围 77%-82%)分析检测胶质母细胞瘤复发的准确性相似。视觉和半定量指标均是 PFS 的显著预测因子,病灶与正常脑组织比值的平均值提供了最佳的鉴别器(平均生存时间,39.4 与 9.3 个月;P <.001)。研究的参数均未预测 OS。
视觉和半定量指标均能以较高的准确性检测胶质母细胞瘤的复发,并预测 PFS。病灶与正常组织比值是 PFS 的最佳鉴别器;然而,研究的参数均未预测 OS。这些回顾性建立的分析参数需要前瞻性验证。