Department of Nuclear Medicine, University Hospital Heidelberg, Heidelberg, Germany
Cooperation Unit Nuclear Medicine, German Cancer Research Center (DKFZ), Heidelberg, Germany.
J Nucl Med. 2018 Apr;59(4):632-635. doi: 10.2967/jnumed.117.196329. Epub 2018 Feb 1.
Biochemical recurrence (BCR) is a concern for prostate cancer patients after local treatment. Ga-labeled prostate-specific membrane antigen (PSMA) ligands have significantly improved prostate cancer imaging. However, several F-labeled ligands that were developed as fluorinated tracers might present advantages. In this study, we analyzed the potential of F-PSMA-1007 in patients with BCR. Twelve patients with BCR after local treatment underwent PET/CT scans 1 and 3 h after injection of F-PSMA-1007. F-PSMA-1007 PET/CT detected lesions in 9 of 12 patients (75%). A significant difference was observed when comparing the tracer uptake in F-PSMA-1007-positive lesions 1 and 3 h after injection (median SUV, 7.00 vs. 11.34; < 0.001; = 76). Forty-four (88%) of 50 F-PSMA-1007-positive lymph nodes had a short-axis diameter of less than 8 mm. In this pilot study, F-PSMA-1007 PET/CT presented high potential for localization of recurrent disease in prostate cancer patients with BCR.
生化复发(BCR)是局部治疗后前列腺癌患者关注的问题。镓标记的前列腺特异性膜抗原(PSMA)配体显著改善了前列腺癌的成像。然而,作为氟代示踪剂开发的几种 F 标记配体可能具有优势。在这项研究中,我们分析了 F-PSMA-1007 在 BCR 患者中的潜力。12 例局部治疗后发生 BCR 的患者在注射 F-PSMA-1007 后 1 小时和 3 小时进行了 PET/CT 扫描。F-PSMA-1007 PET/CT 在 12 例患者中的 9 例(75%)中检测到病变。在注射后 1 小时和 3 小时 F-PSMA-1007 阳性病变的摄取中观察到显著差异(中位数 SUV,7.00 与 11.34;<0.001;=76)。50 个 F-PSMA-1007 阳性淋巴结中有 44 个(88%)短轴直径小于 8 毫米。在这项初步研究中,F-PSMA-1007 PET/CT 显示出在 BCR 前列腺癌患者中定位复发性疾病的高潜力。