Department of Radiology and Nuclear Medicine, Erasmus MC, Rotterdam, Netherlands.
Department of Nuclear Medicine, University of Duisburg-Essen and German Cancer Consortium (DKTK), University Hospital Essen, Essen, Germany.
Eur J Nucl Med Mol Imaging. 2021 Jan;48(1):67-72. doi: 10.1007/s00259-020-05038-9. Epub 2020 Oct 15.
The EC Directive 2013/59/Euratom states in article 56 that exposures of target volumes in nuclear medicine treatments shall be individually planned and their delivery appropriately verified. The Directive also mentions that medical physics experts should always be appropriately involved in those treatments. Although it is obvious that, in nuclear medicine practice, every nuclear medicine physician and physicist should follow national rules and legislation, the EANM considered it necessary to provide guidance on how to interpret the Directive statements for nuclear medicine treatments.For this purpose, the EANM proposes to distinguish three levels in compliance to the optimization principle in the directive, inspired by the indication of levels in prescribing, recording and reporting of absorbed doses after radiotherapy defined by the International Commission on Radiation Units and Measurements (ICRU): Most nuclear medicine treatments currently applied in Europe are standardized. The minimum requirement for those treatments is ICRU level 1 ("activity-based prescription and patient-averaged dosimetry"), which is defined by administering the activity within 10% of the intended activity, typically according to the package insert or to the respective EANM guidelines, followed by verification of the therapy delivery, if applicable. Non-standardized treatments are essentially those in developmental phase or approved radiopharmaceuticals being used off-label with significantly (> 25% more than in the label) higher activities. These treatments should comply with ICRU level 2 ("activity-based prescription and patient-specific dosimetry"), which implies recording and reporting of the absorbed dose to organs at risk and optionally the absorbed dose to treatment regions. The EANM strongly encourages to foster research that eventually leads to treatment planning according to ICRU level 3 ("dosimetry-guided patient-specific prescription and verification"), whenever possible and relevant. Evidence for superiority of therapy prescription on basis of patient-specific dosimetry has not been obtained. However, the authors believe that a better understanding of therapy dosimetry, i.e. how much and where the energy is delivered, and radiobiology, i.e. radiation-related processes in tissues, are keys to the long-term improvement of our treatments.
欧洲理事会指令 2013/59/Euratom 在第 56 条中规定,核医学治疗中的靶体积照射应进行个体化计划,并对其剂量传递进行适当验证。该指令还提到,医学物理专家应始终适当参与这些治疗。尽管在核医学实践中,每个核医学医师和物理学家都应遵循国家规定和立法,这是显而易见的,但 EANM 认为有必要就如何解释核医学治疗中的指令声明提供指导。为此,EANM 建议根据指令中的优化原则区分三个级别,这是受国际辐射单位和测量委员会 (ICRU) 规定的放射治疗后吸收剂量的处方、记录和报告的水平指示的启发:
目前在欧洲应用的大多数核医学治疗都是标准化的。这些治疗的最低要求是 ICRU 级别 1(“基于活性的处方和患者平均剂量测定”),这是通过将活性控制在目标活性的 10% 以内来定义的,通常是根据药物说明书或相应的 EANM 指南进行的,然后根据需要验证治疗的传递。非标准化治疗主要是那些处于开发阶段或根据标签以外的适应证使用的批准放射性药物,其活性显著高于标签(>25%)。这些治疗应符合 ICRU 级别 2(“基于活性的处方和患者特定剂量测定”),这意味着记录和报告危险器官的吸收剂量,并根据需要报告治疗区域的吸收剂量。EANM 强烈鼓励促进研究,以便在可能和相关的情况下,根据 ICRU 级别 3(“剂量引导的患者特定处方和验证”)进行治疗计划。尚未获得基于患者特定剂量测定的治疗方案优越性的证据。然而,作者认为,更好地了解治疗剂量学,即能量的传递量和位置,以及放射生物学,即组织中的辐射相关过程,是我们治疗长期改进的关键。