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诊断剂剂量测定的准确性:基于全器官S值计算中使用的源组织数量的影响。

Accuracy in dosimetry of diagnostic agents: impact of the number of source tissues used in whole organ S value-based calculations.

作者信息

Josefsson Anders, Siritantikorn Klaikangwol, Ranka Sagar, de Amorim de Carvalho Jose Willegaignon, Buchpiguel Carlos Alberto, Sapienza Marcelo Tatit, Bolch Wesley E, Sgouros George

机构信息

Russell H. Morgan Department of Radiology and Radiological Science, Johns Hopkins University, School of Medicine, Baltimore, MD, USA.

Instituto do Cancer do Estado de São Paulo, São Paulo University, School of Medicine, São Paulo, SP, Brazil.

出版信息

EJNMMI Res. 2020 Mar 19;10(1):26. doi: 10.1186/s13550-020-0614-6.

Abstract

BACKGROUND

Dosimetry for diagnostic agents is performed to assess the risk of radiation detriment (e.g., cancer) associated with the imaging agent and the risk is assessed by computing the effective dose coefficient, e. Stylized phantoms created by the MIRD Committee and updated by work performed by Cristy-Eckerman (CE) have been the standard in diagnostic dosimetry. Recently, the ICRP developed voxelized phantoms, which are described in ICRP Publication 110. These voxelized phantoms are more realistic and detailed in describing human anatomy compared with the CE stylized phantoms. Ideally, all tissues should be represented and their pharmacokinetics collected for an as accurate a dosimetric calculation as possible. As the number of source tissues included increases, the calculated e becomes more accurate. There is, however, a trade-off between the number of source tissues considered, and the time and effort required to measure the time-activity curve for each tissue needed for the calculations. In this study, we used a previously published Ga-DOTA-TATE data set to examine how the number of source tissues included for both the ICRP voxelized and CE stylized phantoms affected e.

RESULTS

Depending upon the number of source tissues included e varied between 14.0-23.5 μSv/MBq for the ICRP voxelized and 12.4-27.7 μSv/MBq for the CE stylized phantoms. Furthermore, stability in e, defined as a < 10% difference between e obtained using all source tissues compared to one using fewer source tissues, was obtained after including 5 (36%) of the 14 source tissues for the ICRP voxelized, and after including 3 (25%) of the 12 source tissues for the CE stylized phantoms. In addition, a 2-fold increase in e was obtained when all source tissues where included in the calculation compared to when the TIAC distribution was lumped into a single reminder-of-body source term.

CONCLUSIONS

This study shows the importance of including the larger tissues like the muscles and remainder-of-body in the dosimetric calculations. The range of e based on the included tissues were less for the ICRP voxelized phantoms using tissue weighting factors from ICRP Publication 103 compared to CE stylized phantoms using tissue weighting factors from ICRP Publication 60.

摘要

背景

对诊断剂进行剂量测定是为了评估与成像剂相关的辐射损害(如癌症)风险,该风险通过计算有效剂量系数来评估。由MIRD委员会创建并经克里斯蒂 - 埃克曼(CE)更新的理想化体模一直是诊断剂量测定的标准。最近,国际辐射防护委员会(ICRP)开发了体素化体模,在ICRP第110号出版物中有描述。与CE理想化体模相比,这些体素化体模在描述人体解剖结构方面更逼真、更详细。理想情况下,应涵盖所有组织并收集其药代动力学数据,以进行尽可能准确的剂量计算。随着纳入的源组织数量增加,计算得到的有效剂量系数会变得更准确。然而,在考虑的源组织数量与测量计算所需的每个组织的时间 - 活度曲线所需的时间和精力之间存在权衡。在本研究中,我们使用先前发表的镓 - DOTA - TATE数据集来研究ICRP体素化体模和CE理想化体模所包含的源组织数量如何影响有效剂量系数。

结果

根据纳入的源组织数量,ICRP体素化体模的有效剂量系数在14.0 - 23.5 μSv/MBq之间变化,CE理想化体模的有效剂量系数在12.4 - 27.7 μSv/MBq之间变化。此外,对于ICRP体素化体模,在纳入14个源组织中的5个(36%)后,以及对于CE理想化体模,在纳入12个源组织中的3个(25%)后,有效剂量系数的稳定性得以实现,稳定性定义为使用所有源组织获得的有效剂量系数与使用较少源组织获得的有效剂量系数之间的差异<10%。此外,与将时间 - 活度曲线分布集中到单个身体其余部分源项时相比,当计算中纳入所有源组织时,有效剂量系数增加了2倍。

结论

本研究表明在剂量计算中纳入肌肉和身体其余部分等较大组织的重要性。与使用ICRP第60号出版物中的组织权重因子的CE理想化体模相比,使用ICRP第103号出版物中的组织权重因子的ICRP体素化体模基于所包含组织的有效剂量系数范围更小。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8447/7080914/e3bbb54a83ac/13550_2020_614_Fig1_HTML.jpg

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