论文标题
使用低统计量蒙特卡洛模拟的临床前微束放射治疗研究的准确而快速的深度学习剂量预测
Accurate and fast deep learning dose prediction for a preclinical microbeam radiation therapy study using low-statistics Monte Carlo simulations
论文作者
论文摘要
Microbeam辐射疗法(MRT)利用共面同步辐射束,是目前临床治疗结果(例如胶质肉瘤)的几种肿瘤诊断的建议治疗方法。目前,澳大利亚同步加速器的成像和医疗光束线的MRT研究中处理临床前胶质肉瘤模型的处方剂量估计目前依赖于Monte Carlo(MC)模拟。与50 $ \,μ$ m宽的共面束相关的陡峭剂量梯度对在短时间内对MRT辐射处理场进行精确的MC模拟带来了重大挑战。已经对快速剂量估计方法进行了许多研究。但是,这些方法,包括GPU蒙特卡洛实施和机器学习(ML)模型,对于新颖和新兴的癌症辐射治疗方案(例如MRT)而言,无法使用。在这项工作中,首次提出了在回顾性临床前啮齿动物研究中成功应用快速准确的机器学习剂量预测模型。 ML模型可以预测微梁路径中的峰值剂量和它们之间的山谷剂量,并在啮齿动物患者中递送至胶质肉瘤。 ML模型的预测与低噪声MC模拟相当一致,尤其是在调查的肿瘤体积中。尽管ML模型被故意用MC计算的样品培训,但该协议表现出明显更高的统计不确定性。成功使用高噪声训练集数据样本,这些数据样本可以更快地产生,可以鼓励和加速ML模型转移到新型放射癌疗法中其他未来应用的不同治疗方式中。
Microbeam radiation therapy (MRT) utilizes coplanar synchrotron radiation beamlets and is a proposed treatment approach for several tumour diagnoses that currently have poor clinical treatment outcomes, such as gliosarcomas. Prescription dose estimations for treating preclinical gliosarcoma models in MRT studies at the Imaging and Medical Beamline at the Australian Synchrotron currently rely on Monte Carlo (MC) simulations. The steep dose gradients associated with the 50$\,μ$m wide coplanar beamlets present a significant challenge for precise MC simulation of the MRT irradiation treatment field in a short time frame. Much research has been conducted on fast dose estimation methods for clinically available treatments. However, such methods, including GPU Monte Carlo implementations and machine learning (ML) models, are unavailable for novel and emerging cancer radiation treatment options like MRT. In this work, the successful application of a fast and accurate machine learning dose prediction model in a retrospective preclinical MRT rodent study is presented for the first time. The ML model predicts the peak doses in the path of the microbeams and the valley doses between them, delivered to the gliosarcoma in rodent patients. The predictions of the ML model show excellent agreement with low-noise MC simulations, especially within the investigated tumour volume. This agreement is despite the ML model being deliberately trained with MC-calculated samples exhibiting significantly higher statistical uncertainties. The successful use of high-noise training set data samples, which are much faster to generate, encourages and accelerates the transfer of the ML model to different treatment modalities for other future applications in novel radiation cancer therapies.