Delker Andreas, Ilhan Harun, Zach Christian, Brosch Julia, Gildehaus Franz Josef, Lehner Sebastian, Bartenstein Peter, Böning Guido
Department of Nuclear Medicine, University Hospital, Ludwig-Maximilians-Universität, Munich, Germany.
Mol Imaging Biol. 2015 Oct;17(5):726-34. doi: 10.1007/s11307-015-0839-3.
Multiple measurements have been required to estimate the radiation dose to the kidneys resulting from [(177)Lu]DOTATATE therapy for neuroendocrine tumors. The aim of this study was to investigate the influence of early time-point measurement in the renal dose calculation.
Anterior/posterior whole-body planar scintigraphy images were acquired at approx. 1, 24, 48, and 72 h after administration of [(177)Lu]DOTATATE. Furthermore, we acquired planar 1-bed dynamic recordings in 12 frames (5 min each) during the first hour. We assessed kidney exposure with a three-phase model consisting of a linear increase to the maximum within the initial minutes p.i., followed a bi-exponential decline. This three-phase-model served as reference for evaluating accuracy of dose estimates in 105 kidneys calculated by conventional mono-exponential fitting of the final three and four whole-body images.
Mean effective half-life times for the reference model were 25.8 ± 12.0 min and 63.9 ± 17.6 h, predicting a mean renal dose of 5.7 ± 2.1 Gy. The effective half-life time was 46.3 ± 15.4 h for the last four and 63.3 ± 17.0 h for the last three data points. The mean start of the first whole-body measurement was 1.2 ± 0.1 h p.i. The ratio of fast to slow phases was 28.1 ± 23.9% at this time point, which caused a mean absolute percentage dose deviation of 12.4% for four data points, compared to 3.1% for three data points. At a mean time of 2.4 h p.i. (max 5.1 h), the ratio of fast to slow phase declined below 5%.
Kinetic analysis of renal uptake using dynamic planar scans from the first hour after injection revealed a fast and a slow washout phase. Although the fast phase did not contribute substantially to the estimated renal dose, it could influence planar measurements performed within the first hours. We found that the presence of two clearance phases can hamper accurate dose estimation based on a single-phase model, resulting in approximately 12.4% dose underestimation, thus potentially resulting in overtreatment. In the absence of dynamic initial recordings, the first dosimetry measurements should therefore be obtained later than 3-5 h after [(177)Lu]DOTATATE injection. Omitting the early whole-body image reduced the dose estimation error to 3.1%.
为了估算[(177)Lu]DOTATATE治疗神经内分泌肿瘤时肾脏所接受的辐射剂量,需要进行多次测量。本研究的目的是探讨早期时间点测量对肾脏剂量计算的影响。
在给予[(177)Lu]DOTATATE后约1、24、48和72小时采集前后位全身平面闪烁显像图像。此外,在给药后的第一个小时内,我们采集了12帧(每帧5分钟)的平面单床位动态记录。我们使用一个三相模型评估肾脏的放射性摄取情况,该模型包括注射后最初几分钟内线性增加至最大值,随后呈双指数下降。这个三相模型作为评估通过对最后三幅和四幅全身图像进行常规单指数拟合计算出的105个肾脏剂量估计准确性的参考。
参考模型的平均有效半衰期分别为25.8±12.0分钟和63.9±17.6小时,预测平均肾脏剂量为5.7±2.1 Gy。最后四个数据点的有效半衰期为46.3±15.4小时,最后三个数据点的有效半衰期为63.3±17.0小时。第一次全身测量的平均开始时间为注射后1.2±0.1小时。此时快速相与慢速相的比例为28.1±23.9%,这导致四个数据点的平均绝对剂量百分比偏差为12.4%,而三个数据点的偏差为3.1%。在注射后平均2.4小时(最长5.1小时)时,快速相与慢速相的比例降至5%以下。
注射后第一小时动态平面扫描对肾脏摄取的动力学分析显示出快速和慢速洗脱期。虽然快速相对估计的肾脏剂量贡献不大,但它可能会影响最初几个小时内进行的平面测量。我们发现两个清除期的存在会妨碍基于单相模型的准确剂量估计,导致约12.4%的剂量低估,从而可能导致过度治疗。因此,在没有动态初始记录的情况下,首次剂量测定测量应在注射[(177)Lu]DOTATATE后3 - 5小时之后进行。省略早期全身图像可将剂量估计误差降低至3.1%。