Clinical Evaluation of (4S)-4-(3-[18F]Fluoropropyl)-L-glutamate (18F-FSPG) for PET/CT Imaging in Patients with Newly Diagnosed and Recurrent Prostate Cancer

被引:17
作者
Park, Sonya Youngju [1 ,2 ]
Na, Sae Jung [1 ,3 ]
Kumar, Meena [2 ]
Mosci, Camila [2 ]
Wardak, Mirwais [2 ]
Koglin, Norman [4 ,5 ]
Bullich, Santiago [5 ]
Mueller, Andre [4 ,5 ]
Berndt, Mathias [4 ,5 ]
Stephens, Andrew W. [4 ,5 ]
Cho, Yong Mee [6 ]
Ahn, Hanjong [7 ]
Chae, Sun Young [3 ]
Kim, Hye Ok [3 ,8 ]
Moon, Dae Hyuk [3 ]
Gambhir, Sanjiv S. [2 ,9 ]
Mittra, Erik S. [2 ,10 ]
机构
[1] Catholic Univ Korea, Coll Med, Dept Radiol, Seoul, South Korea
[2] Stanford Univ, Mol Imaging Program Stanford MIPS, Dept Radiol, Stanford, CA 94305 USA
[3] Univ Ulsan, Asan Med Ctr, Dept Nucl Med, Coll Med, Seoul, South Korea
[4] Bayer Pharma AG, Berlin, Germany
[5] Life Mol Imaging GmbH, Berlin, Germany
[6] Univ Ulsan, Asan Med Ctr, Dept Pathol, Coll Med, Seoul, South Korea
[7] Univ Ulsan, Asan Med Ctr, Dept Urol, Coll Med, Seoul, South Korea
[8] Ewha Womans Univ, Dept Nucl Med, Coll Med, Seoul, South Korea
[9] Stanford Univ, Stanford Bio X Program, Dept Mat Sci & Engn, Dept Bioengn, Stanford, CA 94305 USA
[10] Oregon Hlth & Sci Univ, Dept Diagnost Radiol, Portland, OR 97239 USA
关键词
POSITRON-EMISSION-TOMOGRAPHY; X(C)(-) TRANSPORTER ACTIVITY; OXIDATIVE STRESS; LOCALIZATION; CELLS; CD44; (4S)-4-(3-F-18-FLUOROPROPYL)-L-GLUTAMATE; ACID;
D O I
10.1158/1078-0432.CCR-20-0644
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Purpose: (4S)-4-(3-[F-18]Fluoropropyl)-L-glutamic acid (F-18-FSPG) is a radiopharmaceutical for PET imaging of system x(C)(-) activity, which can be upregulated in prostate cancer. We present data on the first evaluation of patients with newly diagnosed or recurrent prostate cancer with this radiopharmaceutical. Experimental Design: Ten patients with primary and 10 patients with recurrent prostate cancer were enrolled in this prospective multicenter study. After injection of 300 MBq of F-18-FSPG, three whole-body PET/CT scans were obtained. Visual analysis was compared with step-section histopathology when available as well as other imaging studies and clinical outcomes. Metabolic parameters were measured semiquantitatively. Expression levels of xCT and CD44 were evaluated by IHC for patients with available tissue samples. Results: F-18-FSPG PET showed high tumor-to-background ratios with a relatively high tumor detection rate on a per-patient (89%) and per-lobe (87%) basis. The sensitivity was slightly higher with imaging at 105 minutes in comparison with 60 minutes. The maximum standardized uptake values (SUVmax) for cancer was significantly higher than both normal (P < 0.005) and benign pathology (P = 0.011), while there was no significant difference between normal and benign pathology (P = 0.120). In the setting of recurrence, agreement with standard imaging was demonstrated in 7 of 9 patients (78%) and 13 of 18 lesions (72%), and revealed true local recurrence in a discordant case. F-18-FSPG accumulation showed moderate correlation with CD44 expression. Conclusions: F-18-FSPG is a promising tumor imaging agent for PET that seems to have favorable biodistribution and high cancer detection rate in patients with prostate cancer. Further studies are warranted to determine the diagnostic value for both initial staging and recurrence, and how it compares with other investigational radiotracers and conventional imaging modalities.
引用
收藏
页码:5380 / 5387
页数:8
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