Molecular Imaging Branch, National Institute of Mental Health, Bethesda, Maryland;
Department of Obstetrics and Gynecology, Niigata University Medical & Dental Hospital, Niigata, Japan; and.
J Nucl Med. 2022 Oct;63(10):1592-1597. doi: 10.2967/jnumed.121.263561. Epub 2022 Feb 3.
The fetal absorbed dose from F-FDG administration to the mother is an essential piece of information when considering the use of PET to stage cancers during pregnancy. However, the few existing human case reports were obtained using either PET-only or PET/CT machines, which may not accurately identify the soft tissues of the fetus for dosimetric calculations. This study presents data from 11 women injected with F-FDG for cancer staging during the first 2 trimesters of pregnancy and is, to our knowledge, the first to be entirely acquired with PET/MRI. Eleven pregnant women (12 scans) with cervical cancer were imaged with F-FDG PET/MRI, and their images were retrospectively analyzed for this study. The fraction of injected activity concentrated by the fetus was derived from manually drawing regions of interest on the MRI slices. From the activity fraction, the fetal time-integrated coefficients were derived and combined with the standard coefficients of the mothers' organs from the ICRP publication 106. The fetal absorbed doses were calculated with OLINDA/EXM 1.1 and a dynamic bladder model. All fetuses after early pregnancy could be accurately delineated because of the coregistered MRI scans. F-FDG activity was unevenly distributed in the fetal body: the hearts and urinary bladders were generally visible, whereas the brain showed lower uptake. The estimated fetal doses were 2.21E-02 mGy/MBq for 1 woman imaged in early pregnancy, 7.38 ± 0.25 E-03 mGy/MBq for 3 women imaged at the end of the first trimester, and 4.92 ± 1.53 E-03 mGy/MBq for 8 women imaged during the second trimester. PET/MR images of pregnant women injected with F-FDG confirm that the fetal F-FDG dose is very low. Therefore, clinically appropriate F-FDG scans in women with cancer should not be withheld because of pregnancy.
在考虑使用 PET 对妊娠期间的癌症进行分期时,从母亲到胎儿的 F-FDG 给药吸收剂量是一个重要信息。然而,少数现有的人体病例报告是使用 PET 或 PET/CT 机器获得的,这些机器可能无法准确识别胎儿的软组织,从而进行剂量计算。本研究报告了 11 名在妊娠前 2 个 trimester 期间因癌症分期而注射 F-FDG 的孕妇的数据,据我们所知,这是首次完全使用 PET/MRI 进行的研究。 对 11 名患有宫颈癌的孕妇(12 次扫描)进行了 F-FDG PET/MRI 成像,并对其图像进行了回顾性分析。胎儿的注射活性分数是从 MRI 切片上手动绘制感兴趣区域得出的。根据活性分数,从 ICRP 出版物 106 中得出胎儿时间积分系数,并将其与母亲器官的标准系数结合起来。使用 OLINDA/EXM 1.1 和动态膀胱模型计算胎儿吸收剂量。 由于进行了 MRI 配准,因此所有妊娠早期后的胎儿都可以准确地描绘出来。F-FDG 活性在胎儿体内分布不均匀:心脏和膀胱通常可见,而大脑摄取较低。1 名孕妇在妊娠早期接受成像时,估计的胎儿剂量为 2.21E-02 mGy/MBq,3 名孕妇在妊娠第 1 trimester 末接受成像时,剂量为 7.38 ± 0.25 E-03 mGy/MBq,8 名孕妇在妊娠第 2 trimester 接受成像时,剂量为 4.92 ± 1.53 E-03 mGy/MBq。 对注射 F-FDG 的孕妇进行 PET/MR 成像证实,胎儿的 F-FDG 剂量非常低。因此,在癌症患者中进行临床适当的 F-FDG 扫描时,不应因怀孕而被拒绝。