PET Center, Department of Nuclear Medicine, The First Affiliated Hospital, School of Medicine, Zhejiang University, Hangzhou 310003, China.
Hell J Nucl Med. 2022 Jan-Apr;25(1):11-18. doi: 10.1967/s002449912431. Epub 2022 Apr 8.
Fluorine-18-2-(3-{1-carboxy-5-[(6-F-flfluoro-pyridine-3-carbonyl)-amino]-pentyl}-ureido)-pentanedioic acid (F-DCFPyL), a novel positron emission tomography/computed tomography (PET/CT) radiotracer that binds to the prostate specific membrane antigen (PSMA), is increasingly used for biochemically recurrent prostate cancer diagnostics. However, the F-DCFPyL characteristics of suspected prostate cancer (SPCa) have been even more rarely described. Herein, in this retrospective study, we describe the clinical impact of F-DCFPyL PET/CT imaging in SPCa.
We retrospectively evaluated the data of 56 SPCa patients who had undergone F-DCFPyL PET/CT studies. These patients were done for primary diagnosis/staging. Positron emission tomography/CT images were analyzed both qualitatively and quantitatively (maximum standardized uptake value (SUVmax) and maximum SUV normalized by lean body mass (SULmax)). Histopathologic diagnosis was taken as reference standard. The optimal cut-off of F-DCFPyL was determined using receiver operating characteristic curve (ROC).
All the patients were confirmed by histopathological examination via prostatectomy or prostate biopsy. Fluorine-18-DCFPyL PET/CT showed higher radiotracer uptake in prostate cancer than that in non-prostate cancer. When SUVmax 5.0 and SULmax 4.0 were cut-off points for determining prostate cancer, the sensitivity of F-DCFPyL was 90%, specificity was 100%, and accuracy was 91.2%. Furthermore, there were highly significant positive correlations between SUVmax, SULmax and serum PSA. On comparison of areas under the curve, no significant difference was seen between SUVmax and SULmax in the sensitivity and specificity of F-DCFPyL PET/CT for PCa identification. However, delayed PET/CT did not improved accuracy in the term of uncertain PCa in the initial standard imaging. As for lymph node staging, the negative predictive value of F-DCFPyL PET/CT was 100%.
Fluorine-18-DCFPyL PET/CT is a promising imaging modality for initial diagnosis and preoperative N staging in SPCa.
氟-18-2-[(3-{1-羧基-5-[(6-F-氟吡啶-3-羰基)-氨基]-戊基}-脲基)-戊二酸(F-DCFPyL)是一种新型正电子发射断层扫描/计算机断层扫描(PET/CT)示踪剂,与前列腺特异性膜抗原(PSMA)结合,越来越多地用于生化复发性前列腺癌的诊断。然而,疑似前列腺癌(SPCa)的 F-DCFPyL 特征描述得更少。在此,在这项回顾性研究中,我们描述了 F-DCFPyL PET/CT 成像在 SPCa 中的临床影响。
我们回顾性评估了 56 例接受 F-DCFPyL PET/CT 研究的 SPCa 患者的数据。这些患者是为了进行初步诊断/分期。对正电子发射断层扫描/CT 图像进行了定性和定量分析(最大标准化摄取值(SUVmax)和通过瘦体重归一化的最大 SUV(SULmax))。组织病理学诊断作为参考标准。使用受试者工作特征曲线(ROC)确定 F-DCFPyL 的最佳截断值。
所有患者均通过前列腺切除术或前列腺活检进行组织病理学检查证实。氟-18-DCFPyL PET/CT 显示前列腺癌的放射性示踪剂摄取高于非前列腺癌。当 SUVmax 5.0 和 SULmax 4.0 作为确定前列腺癌的截断点时,F-DCFPyL 的灵敏度为 90%,特异性为 100%,准确性为 91.2%。此外,SUVmax 和 SULmax 与血清 PSA 之间存在高度显著的正相关。在比较曲线下面积时,SUVmax 和 SULmax 在 F-DCFPyL PET/CT 识别前列腺癌的灵敏度和特异性方面无显著差异。然而,在初始标准成像中,不确定的前列腺癌方面,延迟 PET/CT 并不能提高准确性。对于淋巴结分期,F-DCFPyL PET/CT 的阴性预测值为 100%。
氟-18-DCFPyL PET/CT 是 SPCa 初始诊断和术前 N 分期的一种很有前途的成像方式。