Quality assurance in clinical dosimetry.

IF 0.9 4区 医学 Q4 RADIOLOGY, NUCLEAR MEDICINE & MEDICAL IMAGING
Hellenic journal of nuclear medicine Pub Date : 2023-05-01
Manuel Bardiès
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引用次数: 0

Abstract

Introduction: Clinical dosimetry in nuclear medicine is developing fast, with an increasing number of procedures performed for a variety of therapeutic applications. In that context, the advent of CE-marked commercial clinical dosimetry software is a positive signal, as they should, in principle, optimize the workflow and increase robustness. However, they pose the problem of the evaluation of their performances, in terms of accuracy but also ease of use (user-friendliness).

Aim: The aim of this presentation is to discuss the various steps required for the evaluation of clinical dosimetry procedures in general, and dosimetry software in particular.

Materials and methods: The clinical dosimetry workflow (CDW) is the suite of steps that lead from calibration procedures to the final reporting of the clinical dosimetry procedure. The study of the CDW implemented in various software shows a age variability in the implementation of the steps that constitute the CDW, and the order of their implementation. This can be accepted, however it raises the issue of comparing software that, basically, do not do the same thing, or do things in a different order.

Results and discussion: The various steps that compose the CDW have to be studied (benchmarked) using specific tools: If assessing calibrations/reconstructions can be made using phantoms filled with radioactive sources, rigid objects are not adapted to the evaluation of registration procedures. Computing anthropomorphic models can be used to verify absorbed dose calculation algorithms (for example using Monte Carlo radiation transport modelling as the gold standard). As can be seen, a range of tools of different type (test objects, models, patient data) must be used - and sometimes developed - to evaluate each step of the CDW. Finally, the end-to-end process must be benchmarked on "real" clinical data, but the price to pay is that the ground truth is not known, thereby limiting these approaches to precision rather than accuracy.

Conclusion: Nuclear medicine dosimetry quality assurance (QA) is in its infancy. However, procedures already applied in external beam radiotherapy may be easily transposed to nuclear medicine, and it will not take decades until nuclear medicine benefits from sound, reproducible procedures that will increase the robustness of clinical dosimetry procedures.

临床剂量测定的质量保证。
引言:核医学中的临床剂量测定发展迅速,为各种治疗应用进行的程序越来越多。在这种情况下,CE标志的商业临床剂量测定软件的出现是一个积极的信号,因为它们原则上应该优化工作流程并提高稳健性。然而,在准确性和易用性(用户友好性)方面,它们带来了性能评估的问题。目的:本演示的目的是讨论评估临床剂量测定程序所需的各种步骤,尤其是剂量测定软件。材料和方法:临床剂量测定工作流程(CDW)是从校准程序到临床剂量测定程序最终报告的一系列步骤。对各种软件中实现的CDW的研究表明,构成CDW的步骤的实现及其实现顺序存在年龄可变性。这是可以接受的,但它提出了比较软件的问题,这些软件基本上不做相同的事情,或者以不同的顺序做事情。结果和讨论:组成CDW的各个步骤必须使用特定工具进行研究(基准):如果可以使用充满放射源的模型进行校准/重建评估,则刚性物体不适合注册程序的评估。计算拟人模型可用于验证吸收剂量计算算法(例如,使用蒙特卡罗辐射传输模型作为金标准)。可以看出,必须使用一系列不同类型的工具(测试对象、模型、患者数据)——有时还需要开发——来评估CDW的每一步。最后,端到端的过程必须以“真实”的临床数据为基准,但要付出的代价是,基本事实尚不清楚,从而限制了这些方法的准确性而非准确性。结论:核医学剂量测定质量保证(QA)尚处于起步阶段。然而,已经应用于外束放射治疗的程序可能很容易转换为核医学,而且核医学不需要几十年的时间就可以从健全、可重复的程序中受益,从而提高临床剂量测定程序的稳健性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
CiteScore
1.40
自引率
6.70%
发文量
34
审稿时长
>12 weeks
期刊介绍: The Hellenic Journal of Nuclear Medicine published by the Hellenic Society of Nuclear Medicine in Thessaloniki, aims to contribute to research, to education and cover the scientific and professional interests of physicians, in the field of nuclear medicine and in medicine in general. The journal may publish papers of nuclear medicine and also papers that refer to related subjects as dosimetry, computer science, targeting of gene expression, radioimmunoassay, radiation protection, biology, cell trafficking, related historical brief reviews and other related subjects. Original papers are preferred. The journal may after special agreement publish supplements covering important subjects, dully reviewed and subscripted separately.
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