Department of Radiation Oncology, University of Texas Southwestern Medical Center, Dallas, TX 75287, United States of America. Innovative Technologies Of Radiotherapy Computations and Hardware (iTORCH) Laboratory, Department of Radiation Oncology, University of Texas Southwestern Medical Center, Dallas, TX 75287, United States of America.
Phys Med Biol. 2020 Sep 8;65(17):175018. doi: 10.1088/1361-6560/aba40f.
The accuracy of delivered radiation dose and the reproducibility of employed radiotherapy methods are key factors for preclinical radiobiology applications and research studies. In this work, ionization chamber (IC) measurements and Monte Carlo (MC) simulations were used to accurately determine the dose rate for total body irradiation (TBI), a classic radiobiologic and immunologic experimental method. Several phantom configurations, including large solid water slab, small water box and rodentomorphic mouse and rat phantoms were simulated and measured for TBI setup utilizing a preclinical irradiator XRad320. The irradiator calibration and the phantom measurements were performed using an ADCL calibrated IC N31010 following the AAPM TG-61 protocol. The MC simulations were carried out using Geant4/GATE to compute absorbed dose distributions for all phantom configurations. All simulated and measured geometries had favorable agreement. On average, the relative dose rate difference was 2.3%. However, the study indicated large dose rate deviations, if calibration conditions are assumed for a given experimental setup as commonly done for a quick determination of irradiation times utilizing lookup tables and hand calculations. In a TBI setting, the reference calibration geometry at an extended source-to-surface distance and a large reference field size is likely to overestimate true photon scatter. Consequently, the measured and hand calculated dose rates, for TBI geometries in this study, had large discrepancies: 16% for a large solid water slab, 27% for a small water box, and 31%, 36%, and 30% for mouse phantom, rat phantom, and mouse phantom in a pie cage, respectively. Small changes in TBI experimental setup could result in large dose rate variations. MC simulations and the corresponding measurements specific to a designed experimental setup are vital for accurate preclinical dosimetry and reproducibility of radiobiological findings. This study supports the well-recognized need for physics consultation for all radiobiological investigations.
所传递辐射剂量的准确性和所采用放疗方法的可重复性是临床前放射生物学应用和研究的关键因素。在这项工作中,使用电离室(IC)测量和蒙特卡罗(MC)模拟来准确确定全身照射(TBI)的剂量率,这是一种经典的放射生物学和免疫实验方法。为了利用临床前辐照器 XRad320 进行 TBI 设置,模拟并测量了包括大固体水平板、小水盒以及啮齿动物模拟鼠和大鼠模型在内的几种模体配置。根据 AAPM TG-61 协议,使用经过 ADCL 校准的 IC N31010 对辐照器校准和模体测量进行了执行。使用 Geant4/GATE 进行 MC 模拟,以计算所有模体配置的吸收剂量分布。所有模拟和测量的几何形状都具有良好的一致性。平均而言,相对剂量率差异为 2.3%。然而,如果像通常为了利用查找表和手工计算快速确定照射时间而对给定实验设置假设校准条件,则会导致剂量率出现较大偏差。在 TBI 设置中,在扩展源距和大参考场尺寸下的参考校准几何形状可能会高估真实光子散射。因此,在本研究中,对于 TBI 几何形状,测量和手工计算的剂量率之间存在较大差异:大固体水平板为 16%,小水盒为 27%,老鼠模体、老鼠在饼笼中的模体以及大鼠模体分别为 31%、36%和 30%。TBI 实验设置的微小变化可能会导致剂量率的较大变化。特定于设计的实验设置的 MC 模拟和相应的测量对于准确的临床前剂量学和放射生物学结果的可重复性至关重要。本研究支持对所有放射生物学研究进行物理咨询的公认需求。