Lifetime attributable risk of cancer incidence in whole-body 18F-Fluorodeoxyglucose PET/CT scans via 3rd order polynomial approach

H. Murat, M. Kechik, M. T. Chew, I. Kamal, M. A. Said, M. J. Ibahim, M. K. A. Karim
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Abstract

The advent of PET/CT examinations has revolutionized cancer treatment, offering greater precision in diagnosis. Nonetheless, the ionizing radiation exposure during the examination could cause a cancer risk. Hence, this study aimed to evaluate the radiation dose and radiation-induced risk associated of whole-body PET/CT scan that includes the 18F-FDG tracers. For this retrospective study, 40 participants were studied, with an even number of males and females. The average age and weight of the participants were 53.77 ± 15.78 years and 66.59 ± 16.94 kg respectively, and they were administered 424.64 ± 121.19 MBq of 18F-FDG before the PET/CT commenced. The IDAC-Dose 2.1 program was employed to calculate the absorbed dose and effective dose in organs such as the bladder, brain, lung, kidneys, colon, red bone marrow (RBM), stomach, liver, and thyroid. The potential risks of cancer were evaluated using the lifetime attributable risk (LAR) via a 3rd order polynomial approach based on the information provided in the Biological Effects of Ionizing Radiation (BEIR) VII report. The effective dose was 20.1 ± 7.9 mSv, and the ratio of E to administered activity is 1.612 × 10-2 mSv/MBq, which is in line with the ICRP standard. The study found that the average incidence of cancer among men and women was 7 and 8 cases per 100,000 examinations, respectively, with effective dose between 3.2 mSv to 27.3 mSv. In summary, the risk of cancer associated with current whole-body 18F-FDG PET/CT examinations is low, but it is essential to mitigate radiation exposure during these examinations and utilize suitable techniques to prevent stochastic effects from low-dose radiation exposure.
通过三阶多项式方法计算全身 18F 氟脱氧葡萄糖 PET/CT 扫描中癌症发病率的终生归因风险
PET/CT 检查的出现彻底改变了癌症治疗,使诊断更加精确。然而,检查过程中的电离辐射照射可能会导致癌症风险。因此,本研究旨在评估全身 PET/CT 扫描(包括 18F-FDG 示踪剂)的辐射剂量和辐射诱发风险。在这项回顾性研究中,有 40 名参与者接受了研究,其中男性和女性人数相等。参与者的平均年龄和体重分别为(53.77 ± 15.78)岁和(66.59 ± 16.94)公斤,他们在 PET/CT 扫描开始前接受了 424.64 ± 121.19 MBq 的 18F-FDG 治疗。采用 IDAC-Dose 2.1 程序计算了膀胱、脑、肺、肾、结肠、红骨髓(RBM)、胃、肝和甲状腺等器官的吸收剂量和有效剂量。根据电离辐射的生物效应(BEIR)VII 报告中提供的信息,通过三阶多项式方法,使用终生可归因风险(LAR)对潜在的癌症风险进行了评估。有效剂量为 20.1 ± 7.9 mSv,E 与施用活度的比率为 1.612 × 10-2 mSv/MBq,符合国际放射防护委员会的标准。研究发现,在有效剂量介于 3.2 mSv 至 27.3 mSv 之间的情况下,男性和女性的癌症平均发病率分别为每 10 万例检查中有 7 例和 8 例。总之,目前与全身 18F-FDG PET/CT 检查相关的癌症风险很低,但必须在这些检查过程中减少辐照,并利用适当的技术防止低剂量辐照的随机效应。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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