Hamberg L M, Hunter G J, Alpert N M, Choi N C, Babich J W, Fischman A J
Department of Radiology, Massachusetts General Hospital, Charlestown 02129.
J Nucl Med. 1994 Aug;35(8):1308-12.
The dose uptake ratio (DUR) has been used as a quantitative index of glucose metabolism for tumor classification and monitoring response to treatment. In order to provide consistent results, DUR measurements should be made when the concentration of tracer has reached a plateau. The time of this plateau cannot be identified from a single static acquisition.
In this study, we investigated the changes in DUR as a function of time in eight patients with stage III lung cancer. All patients underwent a quantitative dynamic 18F-FDG PET study before and after treatment and the data were analyzed with a three-compartment model. Using the fitted model parameters, the DUR was predicted at the plateau and intermediate times.
Tumor concentrations of 18F-FDG did not reach a plateau within the 90 min of imaging in any of the pre-treatment studies and only in one case post-treatment. The average time to reach 95% of the plateau value pre-treatment was 298 +/- 42 min (range: 130-500 min); in post-treatment, it was 154 +/- 31 min (range: 65-240 min). The difference between the plateau DUR and the 60-min value was 46% +/- 6% pre-treatment and 17% +/- 5% post-treatment.
These data indicate that DUR can vary widely with the time of measurement and that DUR should be interpreted with caution in any individual patient.
剂量摄取率(DUR)已被用作肿瘤分类和治疗反应监测中葡萄糖代谢的定量指标。为了获得一致的结果,应在示踪剂浓度达到平台期时进行DUR测量。仅通过一次静态采集无法确定该平台期的时间。
在本研究中,我们调查了8例III期肺癌患者中DUR随时间的变化情况。所有患者在治疗前后均接受了定量动态18F-FDG PET研究,并使用三室模型对数据进行分析。利用拟合的模型参数,预测了平台期和中间时间点的DUR。
在任何治疗前研究中,18F-FDG的肿瘤浓度在90分钟的成像时间内均未达到平台期,仅在1例治疗后病例中达到。治疗前达到平台期值95%的平均时间为298±42分钟(范围:130 - 500分钟);治疗后为154±31分钟(范围:65 - 240分钟)。平台期DUR与60分钟值之间的差异在治疗前为46%±6%,治疗后为17%±5%。
这些数据表明DUR会随测量时间而有很大变化,在任何个体患者中对DUR的解释都应谨慎。