Department of Radiation Oncology, Amsterdam UMC, Amsterdam 1081, HV, Netherlands. Author to whom any correspondence should be addressed.
Phys Med Biol. 2020 Jun 22;65(12):125012. doi: 10.1088/1361-6560/ab8955.
In the evolving field of adaptive MR guided radiotherapy, the need for dedicated procedures for acceptance and quality assurance is increasing. Research has been devoted to MR compatible dosimeters and phantoms, but to date no end-to-end test has been presented that covers an MRgRT workflow. Such an end-to-end test should comprise each step of the workflow and include all associated uncertainties. The purpose of this study was to investigate the usability of an anthropomorphic deformable and multimodal pelvis (ADAM-pelvis) phantom in combination with film dosimetry for end-to-end testing of an MRgRT adaptive workflow. The ADAM-pelvis phantom included surrogates for muscle tissue, adipose and bone, as well as deformable silicone organs mimicking a prostate patient. At the interfaces of the critical structures (bladder and rectum), small pieces of GafChromic EBT3 films were placed to measure delivered dose. Pre-treatment MR imaging of the phantom was used to delineate the prostate, rectum and bladder and to generate a treatment plan to deliver 2 Gy to the prostate. Electron density (ED) map from CT imaging was used for dose calculation after deformable image registration (DIR) to the pre-treatment MR scan. At each fraction, bladder- and rectum filling was varied and a new adapted plan was generated. Dose calculation was performed using both a DIR-based ED map and a CT-based ED map after acquisition of a new CT scan of the phantom at each fraction. All dose calculations were performed taking into account the magnetic field. A good agreement between measured and calculated dose was found using both, the CT-derived and the DIR-based ED map (2.0% and 2.8% dose difference, respectively). The gamma index pass-rate (3%/2 mm) varied from 96.4% to 100%.The ADAM-pelvis phantom was suitable for end-to-end testing in MR-guided radiotherapy and a very good agreement with the calculated dose was achieved.
在不断发展的自适应磁共振引导放射治疗领域,对专用验收和质量保证程序的需求日益增加。研究致力于开发磁共振兼容剂量计和体模,但迄今为止,尚未提出涵盖整个 MRgRT 工作流程的端到端测试。这样的端到端测试应包括工作流程的每个步骤,并包括所有相关的不确定性。本研究旨在探讨使用仿体变形和多模态骨盆(ADAM-骨盆)体模结合胶片剂量测定进行 MRgRT 自适应工作流程的端到端测试的可用性。ADAM-骨盆体模包括肌肉组织、脂肪和骨骼的替代品,以及模仿前列腺患者的可变形硅酮器官。在关键结构(膀胱和直肠)的界面处,放置小块 GafChromic EBT3 胶片以测量传递的剂量。对体模进行预处理的磁共振成像用于描绘前列腺、直肠和膀胱,并生成计划以向前列腺提供 2 Gy 的剂量。使用 CT 成像的电子密度(ED)图在进行变形图像配准(DIR)到预处理的 MR 扫描后进行剂量计算。在每个分次中,改变膀胱和直肠的充盈度,并生成新的适应性计划。在每次分次中获得体模的新 CT 扫描后,使用基于 DIR 的 ED 图和基于 CT 的 ED 图进行剂量计算。所有剂量计算都考虑了磁场。使用 CT 衍生和 DIR 基于的 ED 图均发现测量剂量与计算剂量之间具有良好的一致性(分别为 2.0%和 2.8%的剂量差异)。伽玛指数通过率(3%/2mm)从 96.4%变化到 100%。ADAM-骨盆体模适用于磁共振引导放射治疗的端到端测试,并与计算剂量具有非常好的一致性。