Silosky Michael S, Karki Ramesh, Morgan Rustain, Anderson Janet, Chin Bennett B
Department of Radiology, Division of Nuclear Medicine, University of Colorado School of Medicine Anschutz Medical Campus Aurora, CO, USA.
Department of Radiology, Division of Nuclear Medicine, University of Colorado Hospital, University of Colorado Health System Aurora, CO, USA.
Am J Nucl Med Mol Imaging. 2021 Feb 15;11(1):27-39. eCollection 2021.
Ga DOTATATE PET/CT protocols are similar to F FDG protocols despite differences in physical properties, biodistribution, and tumor uptake. The purpose of this study is to evaluate the impact of scan time (counts), and target activity on signal-to-noise ratio (SNR) in various sized targets, or lesions. To evaluate this, phantom experiments and analysis of clinical Ga DOTATATE PET/CT studies were performed.
Ga was first compared to F in phantom studies to evaluate recovery coefficients and SNR. Ga phantom studies were also acquired in list mode, and at varying target activities to evaluate the effects of acquisition time and high target concentrations on SNR in clinically relevant small (8 mm) and larger targets (≥ 12 mm). Clinical studies (n = 50) were analyzed to determine if phantom target concentrations and SNR are present in clinical Ga DOTATATE studies at similarly very high tumor activity concentrations (n = 159).
In phantoms, recovery coefficient and SUV for Ga were ~87% of F. SNR for Ga was ~65% of F. For the Ga small target (8 mm) at standard T/B = 2.4, increasing scan time from 5 to 15 minutes increased SNR from < 1 to 1.6, and did not result in target identification. Increasing T/B from 2.4 to 10.9, however, dramatically increased SNR from < 1 to 22.3. Increased T/B resulted in clear visibility of the 8 mm target, even for 1-minute scans. In patients, high hepatic tumor SUV (27.3±29.6), resulted in high SNR (12.5±9.8). For extrahepatic tumors, high SUV (41.6±42.8), resulted in high SNR (43.8±49.9).
Very high target or T/B, even in small targets, can offset the physical limitations of Ga. High target uptake and high T/B are primary factors influencing small lesion detectability.
尽管镓[⁶⁸Ga] DOTATATE PET/CT协议在物理性质、生物分布和肿瘤摄取方面存在差异,但其与氟[¹⁸F] FDG协议相似。本研究的目的是评估扫描时间(计数)和靶活性对各种大小靶区或病变的信噪比(SNR)的影响。为评估此影响,进行了体模实验和对临床镓[⁶⁸Ga] DOTATATE PET/CT研究的分析。
在体模研究中,首先将镓[⁶⁸Ga]与氟[¹⁸F]进行比较,以评估恢复系数和信噪比。镓[⁶⁸Ga]体模研究也以列表模式进行,并在不同的靶活性下进行,以评估采集时间和高靶浓度对临床相关小靶区(8毫米)和较大靶区(≥12毫米)信噪比的影响。分析了50例临床研究,以确定在临床镓[⁶⁸Ga] DOTATATE研究中,在类似的非常高的肿瘤活性浓度下(159个)是否存在存在存在存在体模靶浓度和信噪比。
在体模中,镓[⁶⁸Ga]的恢复系数和SUV约为氟[¹⁸F]的87%。镓[⁶⁸Ga]的信噪比约为氟[¹⁸F]的65%。对于标准T/B = 2.4时的镓[⁶⁸Ga]小靶区(8毫米),扫描时间从5分钟增加到15分钟,信噪比从<1增加到1.6,且未实现靶区识别。然而,将T/B从2.4增加到10.9,显著将信噪比从<1增加到22.3。T/B增加导致8毫米靶区清晰可见,即使是1分钟扫描。在患者中,肝脏肿瘤SUV高(27.3±29.6),导致信噪比高(12.5±9.8)。对于肝外肿瘤,SUV高(41.6±42.8),导致信噪比高(43.8±49.9)。
即使在小靶区,非常高的靶区或T/B也可以抵消镓[⁶⁸Ga]的物理限制。高靶摄取和高T/B是影响小病变可检测性的主要因素。