Prospective comparison of (4S)-4-(3-18F-fluoropropyl)-l-glutamate versus 18F-fluorodeoxyglucose PET/CT for detecting metastases from pancreatic ductal adenocarcinoma: a proof-of-concept study

被引:19
作者
Cheng, Mei-Fang [1 ,2 ]
Huang, Ya-Yao [1 ,2 ]
Ho, Bing-Ying [2 ,3 ,4 ]
Kuo, Ting-Chun [2 ,3 ]
Hsin, Ling-Wei [5 ,6 ,7 ]
Shiue, Chyng-Yann [1 ,2 ,6 ]
Kuo, Hsun-Chuan [2 ,3 ]
Jeng, Yung-Ming [2 ,8 ]
Yen, Rouh-Fang [1 ,2 ]
Tien, Yu-Wen [2 ,3 ]
机构
[1] Natl Taiwan Univ Hosp, Dept Nucl Med, Taipei, Taiwan
[2] Natl Taiwan Univ, Coll Med, 7 Chung Shan South Rd, Taipei 10002, Taiwan
[3] Natl Taiwan Univ Hosp, Dept Surg, 7 Chung Shan South Rd, Taipei 10002, Taiwan
[4] Taipei Med Univ, Dept Anesthesiol, Wang Fang Hosp, Taipei, Taiwan
[5] Natl Taiwan Univ, Sch Pharm, Taipei, Taiwan
[6] Natl Taiwan Univ, Mol Imaging Ctr, Taipei, Taiwan
[7] Natl Taiwan Univ, Ctr Innovat Therapeut Discovery, Taipei, Taiwan
[8] Natl Taiwan Univ Hosp, Dept Pathol, Taipei, Taiwan
关键词
Pancreatic cancer; Liver metastases; Positron emission tomography; FSPG; xC transporter system; X(C)(-) TRANSPORTER ACTIVITY; CYSTINE/GLUTAMATE ANTIPORTER; CANCER; TOMOGRAPHY; MANAGEMENT; RESECTION; ACID; XCT;
D O I
10.1007/s00259-018-4251-5
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(4S)-4-(3-F-18-Fluoropropyl)-l-glutamate (FSPG) positron emission tomography (PET) reflects system x(C)(-) transporter (xCT) expression. FSPG PET has been used to detect brain, lung, breast and liver cancer with only modest success. There is no report on the use of FSPG PET in pancreatic ductal adenocarcinoma (PDAC), presumably because of normal xCT expression in the pancreas. Nonetheless, the tissue-specific expression of xCT in the pancreas suggests that FSPG PET may be ideal for identifying metastasized PDAC.MethodsThe performance of FSPG in detecting PDAC metastases was compared with that of F-18-fluorodeoxyglucose (FDG) in small-animal PET studies in seven PDAC tumour-bearing mice and in prospective PET/computed tomography (CT) studies in 23 patients with tissue-confirmed PDAC of stage III or stage IV. All PET/CT results were correlated with the results of histopathology or contrast-enhanced CT (ceCT) performed 3 and 6months later.ResultsIn the rodent model, FSPG PET consistently found more PDAC metastases earlier than FDG PET. FSPG PET showed a trend for a higher sensitivity, specificity and diagnostic accuracy than FDG PET in detecting PDAC metastases in a patient-based analysis: 95.0%, 100.0% and 95.7%, and 90.0%, 66.7% and 90.0%, respectively. In a lesion-based analysis, FSPG PET identified significantly more PDAC metastases, especially in the liver, than FDG PET (109 vs. 95; P=0.0001, 95% CI 4.9-14.6). The tumour-to-background ratios for FSPG and FDG uptake on positive scans were similar (FSPG 4.24.3, FDG 3.6 +/- 3.0; P=0.44, 95% CI -1.11 to 0.48), despite a lower tumour maximum standardized uptake value in FSPG-avid lesions (FSPG 4.2+2.3, FDG 7.7+5.7; P=0.002, 95% CI 0.70-4.10). Because of the lower physiological activity of FSPG in the liver, FSPG PET images of the liver are more easy to interpret than FDG PET images, and therefore the use of FSPG improves the detection of liver metastasis.ConclusionFSPG PET is superior to FDG PET in detecting metastasized PDAC, especially in the liver.
引用
收藏
页码:810 / 820
页数:11
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