Key Laboratory of Radiopharmaceuticals, Ministry of Education, College of Chemistry, Beijing Normal University, Beijing, China.
Clin Nucl Med. 2018 Nov;43(11):e392-e399. doi: 10.1097/RLU.0000000000002257.
There is a need for an alternative PET probe, which does not show normal brain tissue uptake in the evaluation of metastasis to the brain. Therefore, we investigate the feasibility of F-labeled glutamine analog, F-(2S,4R)-4-fluoroglutamine (F-FGln), as a new metabolic probe to detect brain metastasis.
Patients (7 men and 7 women; age, 25-67 years) with suspected brain metastasis were enrolled for this study. All patients were imaged first with F-FGln PET (3 patients for 1-hour dynamic whole-body PET/CT scans, and 11 patients for static whole-body scans at 30 ± 10 minutes after injection), followed by a whole-body F-FDG PET performed in the same week. The characteristics of F-FGln PET imaging in brain metastasis patients were compared with that of F-FDG PET and/or contrast-enhanced MRI patient-by-patient. A composite of all functional and anatomic imaging studies served as the imaging comparator.
Initial study in 3 patients using 1-hour dynamic scan showed that 30 ± 10 minutes after injection is optimal for identifying brain metastasis with a high-contrast ratio. All patients were positive for brain metastasis on this studies that demonstrated 38 lesions in 6 anatomic regions on the imaging comparator. The per-lesion detection rates for F-FGln PET and F-FDG PET were 81.6% and 36.8%, respectively. The average tumor-to-normal brain ratio of F-FGln PET was significantly better than that of F-FDG PET in all patients (4.97 ± 2.23 vs 1.22 ± 0.69, P < 0.05). Furthermore, our results suggest that F-FGln uptake in brain metastasis appeared to be independent of tumor size and peripheral edema. In addition, in 14 brain metastatic lesions visualized by both F-FDG PET and F-FGln PET imaging, a positive correlation of SUVmax was observed (r = 0.780, P < 0.01). As to the extracranial metastasis, both tracers showed a concordant increased radioactive uptake except in liver and bone.
The initial imaging of F-FGln presenting a promising new PET radiotracer for patients with brain metastasis and its utility in the liver and bone metastatic lesions may require more caution due to uptake in normal structures.
需要一种替代的 PET 探针,它在评估脑转移时不会显示正常脑组织摄取。因此,我们研究了 F-标记的谷氨酰胺类似物 F-(2S,4R)-4-氟谷氨酰胺(F-FGln)作为一种新的代谢探针来检测脑转移的可行性。
本研究纳入了 7 名男性和 7 名女性疑似脑转移患者(年龄 25-67 岁)。所有患者均首先进行 F-FGln PET 成像(3 名患者进行 1 小时动态全身 PET/CT 扫描,11 名患者在注射后 30±10 分钟进行静态全身扫描),然后在同一周内进行全身 F-FDG PET 扫描。逐个患者比较 F-FGln PET 成像在脑转移患者中的特征与 F-FDG PET 和/或对比增强 MRI 的特征。所有功能和解剖成像研究的组合作为成像比较器。
在 3 名患者的初步研究中,使用 1 小时动态扫描显示,在注射后 30±10 分钟时,识别脑转移的对比度最佳。在成像比较器上,所有患者的脑转移均为阳性,显示 6 个解剖区域的 38 个病变。F-FGln PET 和 F-FDG PET 的病变检出率分别为 81.6%和 36.8%。在所有患者中,F-FGln PET 的肿瘤与正常脑比值明显优于 F-FDG PET(4.97±2.23 比 1.22±0.69,P<0.05)。此外,我们的结果表明,脑转移中的 F-FGln 摄取似乎与肿瘤大小和周围水肿无关。此外,在 F-FDG PET 和 F-FGln PET 成像均可见的 14 个脑转移病变中,观察到 SUVmax 的正相关(r=0.780,P<0.01)。对于颅外转移,除肝脏和骨骼外,两种示踪剂均显示放射性摄取增加。
F-FGln 的初步成像表现出作为脑转移患者的一种很有前途的新型 PET 放射性示踪剂,其在肝脏和骨骼转移病变中的应用可能需要更加谨慎,因为它在正常结构中有摄取。