Department of Physics, Royal Marsden Hospital, Downs Road, Sutton, Surrey, United Kingdom.
Department of Nuclear Medicine, Royal Marsden Hospital, Downs Road, Sutton, Surrey, SM2 5PT, United Kingdom.
Br J Radiol. 2021 Mar 1;94(1119):20200072. doi: 10.1259/bjr.20200072. Epub 2020 Sep 9.
There is continuing debate concerning the risks of secondary malignancies from low levels of radiation exposure. The current model used for radiation protection is predicated on the assumption that even very low levels of exposure may entail risk. This has profound implications for medical procedures involving ionising radiation as radiation doses must be carefully monitored, and for diagnostic procedures are minimised as far as possible. This incurs considerable expense. The SOLLID study (ClinicalTrials.gov Identifier: NCT03580161) aims to develop the methodology to enable a large-scale epidemiological investigation of the effect of radiopharmaceutical administrations to patients undergoing diagnostic nuclear medicine procedures. Patients will undergo a series of scans in addition to that acquired as standard of care to enable the radiation doses delivered to healthy organs to be accurately calculated. Detailed analysis will be performed to determine the uncertainty in the radiation dose calculations as a function of the number and type of scans acquired. It is intended that this will inform a subsequent long-term multicentre epidemiological study that would address the question definitively. Secondary aims of the study are to evaluate the range of absorbed doses that are delivered from diagnostic nuclear medicine procedures and to use current risk models to ascertain the relative risks from these administrations.
关于低水平辐射暴露导致继发性恶性肿瘤的风险,一直存在争议。目前用于辐射防护的模型基于这样一种假设,即即使是非常低水平的暴露也可能存在风险。这对涉及电离辐射的医疗程序产生了深远的影响,因为必须仔细监测辐射剂量,并且尽可能减少诊断程序。这会带来相当大的费用。SOLLID 研究(ClinicalTrials.gov 标识符:NCT03580161)旨在开发方法学,以便对接受诊断核医学程序的患者进行放射性药物给药影响的大规模流行病学研究。除了标准护理中获得的扫描外,患者还将进行一系列扫描,以便准确计算健康器官接受的辐射剂量。将进行详细分析,以确定辐射剂量计算的不确定性作为获取的扫描数量和类型的函数。目的是为随后的长期多中心流行病学研究提供信息,从而明确回答这个问题。该研究的次要目标是评估从诊断核医学程序中传递的吸收剂量范围,并使用当前的风险模型来确定这些给药的相对风险。