Department of Nuclear Medicine, Ghent University Hospital, Ghent, Belgium.
Clin Nucl Med. 2013 Jul;38(7):495-500. doi: 10.1097/RLU.0b013e318292a753.
The aim of this study was to validate 18F-FDG PET imaging for differentiating high-grade gliomas (HGGs) from low-grade gliomas (LGGs).
Twenty-one patients with gliomas undergoing a stereotactic biopsy underwent PET scanning at conventional and delayed intervals, diagnostic and stereotactic MR examinations. To calculate the uptake at the biopsy site, a 2-mm voxel was selected. Uptake in this voxel was expressed as a percentage of the average uptake per voxel in the normal brain. The difference in uptake between HGG and LGG at conventional and late intervals and the difference in uptake difference between HGG and LGG at both intervals were analyzed using t tests as well as a mixed-model analysis of variance.
At conventional intervals, uptake in LGG was 67% of that in the normal brain. Between early and late intervals, a significant decrease in uptake of 11% (±2.5%) was noted (P = 0.001). Uptake in HGG at conventional intervals was 138% of that in the normal brain. Between early and late intervals, a significant increase in uptake of 43% (±11%) was noted (P = 0.005). The difference in uptake between HGG and LGG was significant both at conventional and delayed intervals (P < 0.001). Moreover, the difference in uptake between both groups was significantly greater (31%) at delayed than at conventional intervals (2%) (P < 0.001).
The results of this correlative study between tumor grade and 18F-FDG uptake both determined at the stereotactic biopsy site indicate that PET, particularly at delayed intervals, is valid for discriminating LGG from HGG.
本研究旨在验证 18F-FDG PET 成像在区分高级别胶质瘤(HGG)和低级别胶质瘤(LGG)中的作用。
21 例接受立体定向活检的胶质瘤患者在常规和延迟期进行 PET 扫描、诊断和立体定向磁共振检查。在活检部位选择 2mm 体素,以计算摄取率。摄取率用该体素的平均摄取率与正常脑区平均摄取率的百分比表示。采用 t 检验和混合模型方差分析比较 HGG 和 LGG 在常规和延迟期的摄取差异,以及两者在两个时期的摄取差异。
在常规期,LGG 的摄取率为正常脑的 67%。在早期和晚期之间,摄取率显著下降 11%(±2.5%)(P=0.001)。HGG 在常规期的摄取率为正常脑的 138%。在早期和晚期之间,摄取率显著增加 43%(±11%)(P=0.005)。HGG 和 LGG 之间的摄取差异在常规和延迟期均有统计学意义(P<0.001)。此外,两组之间的摄取差异在延迟期(31%)明显大于常规期(2%)(P<0.001)。
本研究通过立体定向活检部位肿瘤分级与 18F-FDG 摄取相关性分析,结果表明 PET 特别是延迟期,可有效区分 LGG 和 HGG。