载y -90微球肝放射栓塞剂量学的概念和方法

Arnaud Dieudonné, Manuel Sanchez-Garcia, Aurélie Bando-Delaunay, Rachida Lebtahi
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引用次数: 0

摘要

本文旨在以教学的方式介绍与90Y微球肝放射性栓塞相关的剂量测定概念和方法。介绍了医用内辐射剂量形式在放射性栓塞中的应用。这种形式能够简化剂量测定,其中给定组织中的吸收剂量仅取决于其质量和初始活性。这适用于肝、肿瘤和肺剂量测定的单室法、分区模型,以及允许识别多个肿瘤的多室法。还讨论了基于体素的剂量测定方法。这允许考虑隔间内的不均匀吸收,这转化为不均匀的剂量分布,表示为剂量-体积直方图。为此,剂量核卷积允许以计算高效的方式在体素源周围传播能量沉积。或者,当空间分辨率与β粒子路径相当或大于β粒子路径时,局部能量沉积是优选的。统计工具可能与在特定人群中建立剂量-效应关系有关。其中包括诸如逻辑回归或接收器操作员特征分析之类的工具。举例说明。此外,可以通过Lea和Catcheside的线性二次模型及其对应物Lyman的正常组织并发症概率模型来评估肿瘤控制概率模型,该模型适用于肝脏的平行结构。微球给药的选择性允许保留组织,这可以用等效均匀剂量的概念来考虑,也给出了实例。微球微观沉积的含义也通过肝毒性模型来说明,尽管它没有得到临床验证。最后,我们提出了一个关于治疗指数(TI)概念的反思,这可以通过基于治疗特定参数的TI评估来确定治疗安全性,从而帮助制定治疗计划。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Concepts and methods for the dosimetry of radioembolisation of the liver with Y-90-loaded microspheres.

This article aims at presenting in a didactic way, dosimetry concepts and methods that are relevant for radio-embolization of the liver with 90Y-microspheres. The application of the medical internal radiation dose formalism to radio-embolization is introduced. This formalism enables a simplified dosimetry, where the absorbed dose in a given tissue depends on only its mass and initial activity. This is applied in the single-compartment method, partition model, for the liver, tumour and lung dosimetry, and multi-compartment method, allowing identification of multiple tumours. Voxel-based dosimetry approaches are also discussed. This allows taking into account the non-uniform uptake within a compartment, which translates into a non-uniform dose distribution, represented as a dose-volume histogram. For this purpose, dose-kernel convolution allows propagating the energy deposition around voxel-sources in a computationally efficient manner. Alternatively, local-energy deposition is preferable when the spatial resolution is comparable or larger than the beta-particle path. Statistical tools may be relevant in establishing dose-effect relationships in a given population. These include tools such as the logistic regression or receiver operator characteristic analysis. Examples are given for illustration purpose. Moreover, tumour control probability modelling can be assessed through the linear-quadratic model of Lea and Catcheside and its counterpart, the normal-tissue complication probability model of Lyman, which is suitable to the parallel structure of the liver. The selectivity of microsphere administration allows tissue sparing, which can be considered with the concept of equivalent uniform dose, for which examples are also given. The implication of microscopic deposition of microspheres is also illustrated through a liver toxicity model, even though it is not clinically validated. Finally, we propose a reflection around the concept of therapeutic index (TI), which could help tailor treatment planning by determining the treatment safety through the evaluation of TI based on treatment-specific parameters.

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