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MIRD 手册第 30 号:MIRDfit——用于拟合内部剂量学生物分布时间-活性数据的工具。

MIRD Pamphlet No. 30: MIRDfit-A Tool for Fitting of Biodistribution Time-Activity Data for Internal Dosimetry.

机构信息

Department of Medical Physics, Memorial Sloan Kettering Cancer Center, New York, New York;

Department of Medical Physics, Memorial Sloan Kettering Cancer Center, New York, New York.

出版信息

J Nucl Med. 2024 Nov 1;65(11):1808-1814. doi: 10.2967/jnumed.124.268011.

Abstract

In nuclear medicine, estimating the number of radioactive decays that occur in a source organ per unit administered activity of a radiopharmaceutical (i.e., the time-integrated activity coefficient [TIAC]) is an essential task within the internal dosimetry workflow. TIAC estimation is commonly derived by least-squares fitting of various exponential models to organ time-activity data (radiopharmaceutical biodistribution). Rarely, however, are methods used to objectively determine the model that best characterizes the data. Additionally, the uncertainty associated with the resultant TIAC is generally not evaluated. As part of the MIRDsoft initiative, MIRDfit has been developed to offer a biodistribution fitting software solution that provides the following essential features and advantages for internal dose assessment: nuclear medicine-appropriate fit functions; objective metrics for guiding best-fit selection; TIAC uncertainty calculation; quality control and data archiving; integration with MIRDcalc software for dose calculation; and a user-friendly Excel-based interface. For demonstration and comparative validation of MIRDfit's performance, TIACs were derived from serial imaging studies involving F-FDG and Lu-DOTATATE using MIRDfit. These TIACs were then compared with TIAC estimates obtained using other software. In most cases, the TIACs agreed within approximately 10% between MIRDfit and the other software. MIRDfit has been endorsed by the MIRD Committee of the Society of Nuclear Medicine and Molecular Imaging and has been integrated into the MIRDsoft suite of free dosimetry software; it is available for download at no user cost (https://mirdsoft.org/).

摘要

在核医学中,估计放射性药物在单位给药活度下在源器官中发生的放射性衰变次数(即时间积分活度系数[TIAC])是内部剂量学工作流程中的一项基本任务。TIAC 的估计通常通过将各种指数模型拟合到器官时间-活性数据(放射性药物生物分布)来获得。然而,很少有方法用于客观地确定最能描述数据的模型。此外,与所得 TIAC 相关的不确定性通常未得到评估。作为 MIRDsoft 计划的一部分,MIRDfit 已经开发出来,为内部剂量评估提供了以下基本功能和优势的生物分布拟合软件解决方案:适合核医学的拟合函数;用于指导最佳拟合选择的客观指标;TIAC 不确定性计算;质量控制和数据存档;与 MIRDcalc 软件集成进行剂量计算;以及用户友好的基于 Excel 的界面。为了演示和比较 MIRDfit 的性能,使用 MIRDfit 从涉及 F-FDG 和 Lu-DOTATATE 的系列成像研究中得出了 TIAC。然后将这些 TIAC 与使用其他软件获得的 TIAC 估计值进行比较。在大多数情况下,MIRDfit 和其他软件之间的 TIAC 差异在 10%左右。MIRDfit 已得到核医学和分子成像学会的 MIRD 委员会的认可,并已集成到 MIRDsoft 免费剂量学软件套件中;可在无用户成本的情况下下载(https://mirdsoft.org/)。

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