Department of Radiology and Research Institute of Radiology, University of Ulsan College of Medicine, Asan Medical Center, Seoul, 138-736, Korea.
Department of Radiology, Soonchunhyang University Bucheon Hospital, 170 Jomaru-ro, Wonmi-gu, Bucheon, 420-767, Korea.
Eur Radiol. 2018 Aug;28(8):3285-3295. doi: 10.1007/s00330-018-5341-2. Epub 2018 Feb 27.
To compare the diagnostic performance of amide proton transfer (APT) imaging and 11-C methionine positron emission tomography (MET-PET) for in vivo molecular imaging of protein metabolism in post-treatment gliomas.
This study included 43 patients (12 low and 31 high grade) with post-treatment gliomas who underwent both APT and MET-PET imaging within 3 weeks. APT-weighted voxel values and semi-quantitative tumour-to-normal ratios (TNR) were obtained from tumour portions. The voxel-wise relationships between TNR and APT were assessed. The diagnostic performance for recurrence of high-grade gliomas was calculated, using the area under the receiver operating characteristic curve (AUC) with maximum (TNR and APT) and 90% histogram values (TNR90 and APT90).
A moderate positive correlation between TNR and APT was found in low-grade recurrences (r = 0.47, p < 0.001), but not in high-grade ones (r = -0.24, p < 0.001). For distinguishing recurrence in post-treatment high-grade gliomas, APT (AUC, 0.88) and APT90 (AUC, 0.78-0.83) had a similar to better diagnostic performance than TNR (AUC, 0.71, p = 0.08) or TNR90 (AUC, 0.53-0.59, p = 0.01-0.05).
In post-treatment high-grade gliomas, APT provides different regional information to MET-PET and provides higher diagnostic performance. This difference needs to be considered when using APT or MET-PET as a surrogate marker for tumour protein metabolism.
• APT and TNR values in low-grade recurrence showed a moderate voxel-wise correlation. • APT and TNR demonstrated regional differences in post-treatment high-grade gliomas. • APT90 showed better diagnostic performance than TNR90 in high-grade recurrence.
比较酰胺质子转移(APT)成像和 11-C 蛋氨酸正电子发射断层扫描(MET-PET)在治疗后胶质瘤体内蛋白质代谢分子成像中的诊断性能。
本研究纳入了 43 例治疗后胶质瘤患者(12 例低级别和 31 例高级别),他们在 3 周内同时进行了 APT 和 MET-PET 成像。从肿瘤部位获得 APT 加权体素值和半定量肿瘤与正常比值(TNR)。评估了 TNR 与 APT 之间的体素关系。使用最大(TNR 和 APT)和 90%直方图值(TNR90 和 APT90)的接收器操作特征曲线(AUC)下面积计算高级别胶质瘤复发的诊断性能。
在低级别复发中,TNR 与 APT 之间存在中度正相关(r = 0.47,p < 0.001),但在高级别复发中无相关性(r = -0.24,p < 0.001)。对于鉴别治疗后高级别胶质瘤的复发,APT(AUC,0.88)和 APT90(AUC,0.78-0.83)的诊断性能与 TNR(AUC,0.71,p = 0.08)或 TNR90(AUC,0.53-0.59,p = 0.01-0.05)相似或更好。
在治疗后高级别胶质瘤中,APT 提供了比 MET-PET 更丰富的区域信息,具有更高的诊断性能。在将 APT 或 MET-PET 作为肿瘤蛋白代谢的替代标志物时,需要考虑这种差异。
• 低级别复发中 APT 和 TNR 值具有中度体素相关性。• APT 和 TNR 在治疗后高级别胶质瘤中表现出区域差异。• APT90 在高级别复发中的诊断性能优于 TNR90。