Use of a neural network‐based prediction method to calculate the therapeutic dose in boron neutron capture therapy of patients with glioblastoma

中子俘获 中子 放射治疗 核医学 中子温度 放射治疗计划 胶质母细胞瘤 蒙特卡罗方法 中子源 相对生物效应 医学物理学 材料科学 计算机科学 辐射 医学 物理 核物理学 数学 放射科 统计 癌症研究
作者
Feng Tian,Sheng Zhao,Changran Geng,Chang Guo,Renyao Wu,Xiaobin Tang
出处
期刊:Medical Physics [Wiley]
卷期号:50 (5): 3008-3018 被引量:20
标识
DOI:10.1002/mp.16215
摘要

BACKGROUND: B atoms which selectively concentrated in tumor cells will react with low energy neutrons (mainly thermal neutrons) to produce secondary particles with high linear energy transfer, thus depositing dose in tumor cells. In clinical practice, an appropriate treatment plan needs to be set on the basis of the treatment planning system (TPS). Existing BNCT TPSs usually use the Monte Carlo method to determine the three-dimensional (3D) therapeutic dose distribution, which often requires a lot of calculation time due to the complexity of simulating neutron transportation. PURPOSE: A neural network-based BNCT dose prediction method is proposed to achieve the rapid and accurate acquisition of BNCT 3D therapeutic dose distribution for patients with glioblastoma to solve the time-consuming problem of BNCT dose calculation in clinic. METHODS: The clinical data of 122 patients with glioblastoma are collected. Eighteen patients are used as a test set, and the rest are used as a training set. The 3D-UNET is constructed through the design optimization of input and output data sets based on radiation field information and patient CT information to enable the prediction of 3D dose distribution of BNCT. RESULTS: ), the relative deviation between predicted and simulated results are all less than 2%. The average 2 mm/2% gamma index is 89.67%, and the average 3 mm/3% gamma index is 96.78%. The calculation takes about 6 h to simulate the 3D therapeutic dose distribution of a patient with glioblastoma by Monte Carlo method using Intel Xeon E5-2699 v4, whereas the time required by the method proposed in this study is almost less than 1 s using a Titan-V graphics card. CONCLUSIONS: This study proposes a 3D dose prediction method based on 3D-UNET architecture in BNCT, and the feasibility of this method is demonstrated. Results indicate that the method can remarkably reduce the time required for calculation and ensure the accuracy of the predicted 3D therapeutic dose-effect. This work is expected to promote the clinical development of BNCT in the future.
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