Department of Radiation Physics, MD Anderson Cancer Center, Houston, United States.
Department of Radiation Oncology, MD Anderson Cancer Center, Houston, United States.
Radiother Oncol. 2021 Aug;161:55-64. doi: 10.1016/j.radonc.2021.05.023. Epub 2021 Jun 3.
Gadolinium-based contrast is often used when acquiring MR images for radiation therapy planning for better target delineation. In some situations, patients may still have residual MRI contrast agents in their tissue while being treated with high-energy radiation. This is especially true when MRI contrast agents are administered during adaptive treatment replanning for patients treated on MR-Linac systems.
The purpose of this study was to analyze the molecular stability of MRI contrast agents when exposed to high energy photons and the associated secondary electrons in a 1.5T MR-Linac system. This was the first step in assessing the safety of administering MRI contrast agents throughout the course of treatment.
Two common MRI contrast agents were irradiated with 7 MV photons to clinical dose levels. The irradiated samples were analyzed using liquid chromatography-high resolution mass spectrometry to detect degradation products or conformational alterations created by irradiation with high energy photons and associated secondary electrons.
No significant change in chemical composition or displacement of gadolinium ions from their chelates was discovered in samples irradiated with 7 MV photons at relevant clinical doses in a 1.5T MR-Linac. Additionally, no significant correlation between concentrations of irradiated MRI contrast agents and radiation dose was observed.
The chemical composition stability of the irradiated contrast agents is promising for future use throughout the course of patient treatment. However, in vivo studies are needed to confirm that unexpected metabolites are not created in biological milieus.
在进行放射治疗计划的磁共振成像(MRI)采集时,常使用钆基造影剂以提高靶区勾画的准确性。在某些情况下,当患者接受高能射线治疗时,其组织中仍可能残留 MRI 造影剂。对于在 MR-Linac 系统上接受自适应治疗计划重订的患者,这种情况尤其如此。
本研究旨在分析在 1.5T MR-Linac 系统中,高能量光子和相关次级电子暴露下 MRI 造影剂的分子稳定性。这是评估在整个治疗过程中给予 MRI 造影剂安全性的第一步。
两种常见的 MRI 造影剂用 7MV 光子进行辐照,达到临床剂量水平。使用液相色谱-高分辨率质谱分析辐照后的样品,以检测由高能光子和相关次级电子辐照产生的降解产物或构象改变。
在 1.5T MR-Linac 中,用 7MV 光子以相关临床剂量辐照的样品,未发现化学组成有明显变化,或镧系元素从其螯合物中发生位移。此外,辐照的 MRI 造影剂浓度与辐射剂量之间也未观察到显著相关性。
辐照造影剂的化学组成稳定性为其在患者治疗全过程中的未来应用提供了希望。然而,需要进行体内研究以确认在生物环境中不会产生意想不到的代谢物。