OncoRay - National Center for Radiation Research in Oncology, Faculty of Medicine and University Hospital Carl Gustav Carus, Technische Universität Dresden, Germany; German Cancer Consortium (DKTK), Partner Site Dresden, and German Cancer Research Center (DKFZ), Germany.
OncoRay - National Center for Radiation Research in Oncology, Faculty of Medicine and University Hospital Carl Gustav Carus, Technische Universität Dresden, Germany; Helmholtz-Zentrum Dresden - Rossendorf, Institute of Radiooncology - OncoRay, Germany.
Radiother Oncol. 2020 May;146:205-212. doi: 10.1016/j.radonc.2020.02.023. Epub 2020 Mar 26.
Proton radiotherapy offers the potential to reduce normal tissue toxicity. However, clinical safety margins, range uncertainties, and varying relative biological effectiveness (RBE) may result in a critical dose in tumor-surrounding normal tissue. To assess potential adverse effects in preclinical studies, image-guided proton mouse brain irradiation and analysis of DNA damage repair was established.
We designed and characterized a setup to shape proton beams with 7 mm range in water and 3 mm in diameter and commissioned a Monte Carlo model for in vivo dose simulation. Cone-beam computed tomography and orthogonal X-ray imaging were used to delineate the right hippocampus and position the mice. The brains of three C3H/HeNRj mice were irradiated with 8 Gy and excised 30 min later. Initial DNA double-strand breaks were visualized by staining brain sections for cell nuclei and γH2AX. Imaged sections were analyzed with an automated and validated processing pipeline to provide a quantitative, spatially resolved radiation damage indicator.
The analyzed DNA damage pattern clearly visualized the radiation effect in the mouse brains and could be mapped to the simulated dose distribution. The proton beam passed the right hippocampus and stopped in the central brain region for all evaluated mice.
We established image-guided proton irradiation of mouse brains. The clinically oriented workflow facilitates (back-) translational studies. Geometric accuracy, detailed Monte Carlo dose simulations, and cell-based assessment enable a biologically and spatially resolved analysis of radiation response and RBE.
质子放疗具有降低正常组织毒性的潜力。然而,临床安全边界、射程不确定性和不同的相对生物效应(RBE)可能导致肿瘤周围正常组织的临界剂量。为了在临床前研究中评估潜在的不良反应,我们建立了质子鼠脑照射的图像引导和 DNA 损伤修复分析。
我们设计并表征了一种在水中具有 7mm 射程和 3mm 直径的质子束成型装置,并为体内剂量模拟开发了一个蒙特卡罗模型。锥形束计算机断层扫描和正交 X 射线成像用于勾画右海马体并定位小鼠。用 8Gy 照射三只 C3H/HeNRj 小鼠的大脑,并在 30 分钟后取出。用核和 γH2AX 染色法对脑切片进行初始 DNA 双链断裂的可视化。通过自动和验证的处理管道对成像切片进行分析,提供定量的、空间分辨的辐射损伤指标。
所分析的 DNA 损伤模式清楚地显示了小鼠大脑中的辐射效应,并可与模拟的剂量分布相对应。质子束穿过右侧海马体,并在所有评估的小鼠的中央脑区停止。
我们建立了图像引导的鼠脑质子照射。面向临床的工作流程促进了(回溯)转化研究。几何精度、详细的蒙特卡罗剂量模拟和基于细胞的评估使辐射反应和 RBE 的生物学和空间分辨率分析成为可能。