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应用于靶向放射性核素治疗 (TRT) 的核素离散 β 剂量核矩阵,用 MCNP5 计算。

Discrete beta dose kernel matrices for nuclides applied in targeted radionuclide therapy (TRT) calculated with MCNP5.

机构信息

Institute of Analysis and Scientific Computing, Vienna University of Technology, Karlsplatz 13, 1040 Vienna, Austria.

出版信息

Med Phys. 2009 Nov;36(11):4890-6. doi: 10.1118/1.3231995.

Abstract

PURPOSE

Radiopharmaceuticals administered in targeted radionuclide therapy (TRT) rely to a great extent not only on beta-emitting nuclides but also on emitters of monoenergetic electrons. Recent advances like combined PET/CT devices, the consequential coregistration of both data, the concept of using beta couples for diagnosis and therapy, respectively, as well as the development of voxel models offer a great potential for developing TRT dose calculation systems similar to those available for external beam treatment planning. The deterministic algorithms in question for this task are based on the convolution of three-dimensional matrices, one representing the activity distribution and the other the dose point kernel. This study aims to report on three-dimensional kernel matrices for various nuclides used in TRT.

METHODS

The Monte Carlo code MCNP5 was used to calculate discrete dose kernels of beta particles including the contributions from their respective secondary radiation in soft tissue for the following nuclides: 32P, 33P, 67Cu, 89Sr, 90Y, 103Rh9m), 131I, 177Lu, 186Re, and 188Re. For each nuclide a kernel cube of 10 x 10 x 10 mm3 was calculated, the dimensions of a voxel being 1 mm3. Additional kernels with voxel sizes of 3 x 3 x 3 mm3 were simulated.

RESULTS

Comparison with the S-value data regarding 32P, 89Sr, 90Y, and 131I of the MIRD committee which were calculated with the EGS4 code showed a very good agreement, the secondary particle transport of 90Y being the only exception. Documented analytical kernels on the other side show deviations very close and very far to the source.

CONCLUSIONS

The good accordance with the only discrete dose kernels published up to date justifies the method chosen. Together with the additional six nuclides, this report provides a considerable database for three-dimensional kernel matrices with regard to beta radionuclides applied in TRT. In contrast to analytical dose point kernels, the discrete kernels elude the problem of overestimation near the source and take energy depositions into account, which occur beyond the range of the continuous-slowing-down approximation (csda range). Recalculation of the 1 x 1 x 1 mm3 kernels to other dose kernels with varying voxel dimensions, cubic or noncubic, is shown to be easily manageable and thereby provides a resolution-independent system of dose calculation.

摘要

目的

放射性药物在靶向放射性核素治疗(TRT)中使用,在很大程度上不仅依赖于β发射核素,而且还依赖于单能电子发射体。最近的进展,如结合正电子发射断层扫描/计算机断层扫描(PET/CT)设备,对这两种数据的相应配准,以及分别使用β对进行诊断和治疗的概念,以及体素模型的发展,为开发类似于外束治疗计划的 TRT 剂量计算系统提供了巨大的潜力。为此任务而提出的确定性算法基于三维矩阵的卷积,一个矩阵代表活性分布,另一个矩阵代表剂量点核。本研究旨在报告用于 TRT 的各种核素的三维核矩阵。

方法

使用蒙特卡罗代码 MCNP5 计算了β粒子的离散剂量核,包括其在软组织中的各自次级辐射的贡献,用于以下核素:32P、33P、67Cu、89Sr、90Y、103Rh(9m)、131I、177Lu、186Re 和 188Re。为每个核素计算了 10x10x10mm3 的核矩阵,体素的尺寸为 1mm3。还模拟了具有 3x3x3mm3 体素尺寸的附加核矩阵。

结果

与 MIRD 委员会关于 32P、89Sr、90Y 和 131I 的 S 值数据的比较表明,与 EGS4 代码计算的结果非常吻合,90Y 的次级粒子传输是唯一的例外。另一方面,已发表的解析核矩阵显示出与源非常接近和非常远的偏差。

结论

与迄今为止唯一发表的离散剂量核矩阵的良好一致性证明了所选择的方法是合理的。结合另外六种核素,本报告提供了一个关于应用于 TRT 的β放射性核素的三维核矩阵的相当大的数据库。与解析剂量点核矩阵相比,离散核矩阵避免了源附近的高估问题,并考虑了超出连续慢化近似(csda 范围)的能量沉积。显示将 1x1x1mm3 核矩阵重新计算为具有不同体素尺寸的其他剂量核矩阵,立方或非立方,是很容易处理的,从而提供了一个与分辨率无关的剂量计算系统。

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