Shields Anthony F, Briston David A, Chandupatla Samatha, Douglas Kirk A, Lawhorn-Crews Jawana, Collins Jerry M, Mangner Thomas J, Heilbrun Lance K, Muzik Otto
Karmanos Cancer Institute, 4100 John R Street, 4 HWCRC, Detroit, MI 48201-2013, USA.
Eur J Nucl Med Mol Imaging. 2005 Nov;32(11):1269-75. doi: 10.1007/s00259-005-1813-0. Epub 2005 Jul 1.
[18F]3'-deoxy-3'-fluorothymidine (FLT) is a thymidine analog developed for imaging tumor proliferation with positron emission tomography (PET). To quantitatively assess images, the blood activities of FLT and its glucuronidated metabolite were measured and its kinetics analyzed. This study sought to limit the number of blood samples needed to measure FLT retention.
Total FLT activity was measured from 18 venous samples obtained over the first hour and dynamic imaging performed on 33 patients (average dose 350 MBq/mmol). The 5-, 10-, 30- and 60-min samples were analyzed to measure the fraction of activity in FLT and its glucuronide. HPLC analysis was compared against a two-step column (Sep-Pak) and metabolic rates measured using full and limited sampling. Probenecid (2 g, oral) was given to two patients to determine whether imaging of the liver improved.
At 60 min, 74% of the blood activity was unmetabolized (range 57-85%). HPLC and Sep-Pak gave comparable results (r=0.97; average difference 2.1%). For kinetic analysis, eight venous samples were sufficient to accurately measure total activity; for metabolite analysis, a single sample at 60 min yielded data with mean errors of 2.2%. The metabolic rate correlated with average SUV (r2=0.85; p=0.0002). An aorta input function gave kinetic results comparable to venous blood (r2=0.82). Probenecid did not improve imaging of the liver.
Dynamic measurements of FLT retention can be used to calculate metabolic rates using a limited set of samples and correction for metabolites measured in a single sample obtained at 60 min.
[18F]3'-脱氧-3'-氟胸腺嘧啶核苷(FLT)是一种用于正电子发射断层扫描(PET)肿瘤增殖成像的胸腺嘧啶类似物。为了定量评估图像,测量了FLT及其葡萄糖醛酸化代谢物的血液活性并分析了其动力学。本研究旨在限制测量FLT滞留所需的血样数量。
在最初的一小时内采集18份静脉血样测量总FLT活性,并对33例患者(平均剂量350 MBq/mmol)进行动态成像。分析5分钟、10分钟、30分钟和60分钟的血样,以测量FLT及其葡萄糖醛酸苷中的活性分数。将高效液相色谱(HPLC)分析与两步柱(Sep-Pak)进行比较,并使用全采样和有限采样测量代谢率。给两名患者口服丙磺舒(2 g)以确定肝脏成像是否改善。
在60分钟时,74%的血液活性未代谢(范围为57-85%)。HPLC和Sep-Pak的结果具有可比性(r=0.97;平均差异2.1%)。对于动力学分析,八份静脉血样足以准确测量总活性;对于代谢物分析,60分钟时的单个血样产生的数据平均误差为2.2%。代谢率与平均标准摄取值(SUV)相关(r2=0.85;p=0.0002)。主动脉输入函数给出的动力学结果与静脉血相当(r2=0.82)。丙磺舒并未改善肝脏成像。
FLT滞留的动态测量可用于通过一组有限的样本计算代谢率,并对在60分钟时获得的单个样本中测量的代谢物进行校正。