Radiation Biophysics Division, Department of Nuclear Medicine, National Research Foundation iThemba LABS, Faure, South Africa.
Department of Electronics and Information Systems, IBiTech-MEDISIP, Ghent University, Ghent, Belgium.
PLoS One. 2021 Mar 5;16(3):e0248193. doi: 10.1371/journal.pone.0248193. eCollection 2021.
We investigated the potential of [18F]fluorodeoxyglucose ([18F]FDG) and [18F]Fluoromethylcholine ([18F]FCho) PET, compared to contrast-enhanced MRI, for the early detection of treatment response in F98 glioblastoma (GB) rats.
When GB was confirmed on T2- and contrast-enhanced T1-weighted MRI, animals were randomized into a treatment group (n = 5) receiving MRI-guided 3D conformal arc micro-irradiation (20 Gy) with concomitant temozolomide, and a sham group (n = 5). Effect of treatment was evaluated by MRI and [18F]FDG PET on day 2, 5, 9 and 12 post-treatment and [18F]FCho PET on day 1, 6, 8 and 13 post-treatment. The metabolic tumor volume (MTV) was calculated using a semi-automatic thresholding method and the average tracer uptake within the MTV was converted to a standard uptake value (SUV).
To detect treatment response, we found that for [18F]FDG PET (SUVmean x MTV) is superior to MTV only. Using (SUVmean x MTV), [18F]FDG PET detects treatment effect starting as soon as day 5 post-therapy, comparable to contrast-enhanced MRI. Importantly, [18F]FDG PET at delayed time intervals (240 min p.i.) was able to detect the treatment effect earlier, starting at day 2 post-irradiation. No significant differences were found at any time point for both the MTV and (SUVmean x MTV) of [18F]FCho PET.
Both MRI and particularly delayed [18F]FDG PET were able to detect early treatment responses in GB rats, whereas, in this study this was not possible using [18F]FCho PET. Further comparative studies should corroborate these results and should also include (different) amino acid PET tracers.
我们研究了 [18F]氟脱氧葡萄糖 ([18F]FDG) 和 [18F]氟甲基胆碱 ([18F]FCho) PET 与对比增强 MRI 相比,在 F98 胶质母细胞瘤 (GB) 大鼠治疗反应的早期检测中的潜力。
当 T2 加权和对比增强 T1 加权 MRI 上确认了 GB 后,动物被随机分为治疗组 (n = 5),接受 MRI 引导的 3D 适形弧形微照射 (20 Gy),同时接受替莫唑胺治疗,以及假手术组 (n = 5)。在治疗后第 2、5、9 和 12 天以及治疗后第 1、6、8 和 13 天,通过 MRI 和 [18F]FDG PET 评估治疗效果。代谢肿瘤体积 (MTV) 使用半自动阈值方法计算,MTV 内的平均示踪剂摄取量转换为标准摄取值 (SUV)。
为了检测治疗反应,我们发现对于 [18F]FDG PET (SUVmean x MTV),仅 MTV 是不够的。使用 (SUVmean x MTV),[18F]FDG PET 可在治疗后第 5 天开始检测治疗效果,与对比增强 MRI 相当。重要的是,[18F]FDG PET 在延迟时间间隔 (240 min p.i.) 更早地检测到治疗效果,在照射后第 2 天开始。在任何时间点,[18F]FCho PET 的 MTV 和 (SUVmean x MTV) 均未发现明显差异。
MRI 和特别是延迟的 [18F]FDG PET 均能够检测 GB 大鼠的早期治疗反应,而在本研究中,使用 [18F]FCho PET 则无法做到这一点。进一步的比较研究应证实这些结果,并且还应包括 (不同的) 氨基酸 PET 示踪剂。