Imaging Brain Metastasis Patients With 18F-(2S,4R)-4-Fluoroglutamine

被引:22
作者
Xu, Xiaoxia [1 ]
Zhu, Hua [1 ]
Liu, Fei [1 ]
Zhang, Yan [2 ]
Yang, Jianhua [1 ]
Zhang, Lifang [2 ]
Zhu, Lin [2 ]
Li, Nan [1 ]
Kung, Hank F. [3 ,4 ]
Yang, Zhi [1 ]
机构
[1] Peking Univ, Canc Hosp & Inst, Dept Nucl Med, Key Lab Carcinogenesis & Translat Res,Minist Educ, Beijing, Peoples R China
[2] Beijing Normal Univ, Coll Chem, Minist Educ, Key Lab Radiopharmaceut, Beijing, Peoples R China
[3] Univ Penn, Dept Radiol, Philadelphia, PA 19104 USA
[4] Capital Med Univ, Beijing Inst Brain Disorders, Beijing, Peoples R China
基金
北京市自然科学基金;
关键词
F-18-(2S; 4R)-4-fluoroglutamine; glutamine metabolism; biodistribution; brain metastasis; FDG; POSITRON-EMISSION-TOMOGRAPHY; GRADE GLIOMAS; TUMORS; PET; METABOLISM; CANCER; GLUTAMINE; F-18-FDG;
D O I
10.1097/RLU.0000000000002257
中图分类号
R8 [特种医学]; R445 [影像诊断学];
学科分类号
1002 ; 100207 ; 1009 ;
摘要
Purpose 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-18-labeled glutamine analog, F-18-(2S,4R)-4-fluoroglutamine (F-18-FGln), as a new metabolic probe to detect brain metastasis. Methods 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-18-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-18-FDG PET performed in the same week. The characteristics of F-18-FGln PET imaging in brain metastasis patients were compared with that of F-18-FDG PET and/or contrast-enhanced MRI patient-by-patient. A composite of all functional and anatomic imaging studies served as the imaging comparator. Results 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-18-FGln PET and F-18-FDG PET were 81.6% and 36.8%, respectively. The average tumor-to-normal brain ratio of F-18-FGln PET was significantly better than that of F-18-FDG PET in all patients (4.97 +/- 2.23 vs 1.22 +/- 0.69, P < 0.05). Furthermore, our results suggest that F-18-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-18-FDG PET and F-18-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. Conclusions The initial imaging of F-18-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.
引用
收藏
页码:E392 / E399
页数:8
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