School of Medicine, Department of Nuclear Medicine, Technical University Munich, Munich, Germany;
Division of Nuclear Medicine, Department of Radiology, Faculty of Medicine, Chulalongkorn University, King Chulalongkorn Memorial Hospital, The Thai Red Cross Society, Bangkok, Thailand.
J Nucl Med. 2021 Jul 1;62(7):968-974. doi: 10.2967/jnumed.120.255661. Epub 2020 Nov 13.
The objective of this retrospective study was to assess the detection rate (DR), positive predictive value (PPV), and correct detection rate (CDR) of F-rhPSMA-7 PET/CT in biochemical recurrence (BCR) of prostate cancer (PCa) after radical prostatectomy (RP) using composite validation. F-rhPSMA-7 PET/CT scans of patients with BCR between July 2017 and June 2018 were retrospectively reviewed. All suspicious lesions were recorded. The reference standard was histopathology or combinations of histopathology, imaging, or prostate-specific antigen (PSA) follow up, defined as composite reference standard. DR was calculated as the proportion of PSMA PET-positive patients to all patients independent of the reference standard, whereas the CDR was the percentage of patients who had at least 1 true-positive PSMA PET lesion localized that corresponded with the reference standard. The PPV was defined as the proportion of patients who had true-positive to all positive findings. The correlation between DR and patient characteristics was evaluated. A total of 532 patients with a median PSA level of 0.97 ng/mL (interquartile range: 0.41-2.46 ng/mL) were included. Of these, 162 patients had composite follow-up at a median duration of 5.6 mo (range: 1.1-14.2 mo). The proportion of patients who had no lesion visualized on PET/CT, localized disease, and any distant metastases (M1) were 20%, 43%, and 37%, respectively. PET DR among all patients was 80%. On a per-patient basis, the PPV of F-rhPSMA-7 PET/CT in the composite cohort was 88%, and the CDR was 70%. The PPV in the histopathology-proven cohort was 91%, and the CDR in this subgroup was 73%. In patients with PSA levels ≥ 1 ng/mL the DR and PPV were 90% and 91%, respectively, resulting in a CDR of 82%. In patients with PSA levels < 1 ng/mL, the DR and PPV were 69% and 85%, respectively, resulting in a CDR of 59%. There was a significant positive correlation between F-rhPSMA-7 PET/CT detection efficacy and stratified PSA levels ( = 0.005), as well as PSA nadir after prostatectomy ( < 0.001). F-rhPSMA-7 PET/CT offers high PPV in BCR after RP. Its CDR is dependent on the prescan PSA value with excellent CDR in patients with PSA ≥ 1 ng/mL.
本回顾性研究的目的是使用复合验证评估前列腺癌(PCa)根治性前列腺切除术后生化复发(BCR)患者 F-rhPSMA-7 PET/CT 的检出率(DR)、阳性预测值(PPV)和正确检出率(CDR)。回顾性分析了 2017 年 7 月至 2018 年 6 月期间 BCR 的患者的 F-rhPSMA-7 PET/CT 扫描。记录所有可疑病灶。参考标准为组织病理学或组织病理学、影像学或前列腺特异性抗原(PSA)随访的组合,定义为复合参考标准。DR 计算为 PSMA PET 阳性患者与独立于参考标准的所有患者的比例,而 CDR 为至少有 1 个与参考标准对应的定位阳性 PSMA PET 病变的患者百分比。PPV 定义为真阳性患者与所有阳性发现的比例。评估了 DR 与患者特征之间的相关性。共纳入 532 例中位 PSA 水平为 0.97ng/mL(四分位距:0.41-2.46ng/mL)的患者。其中,162 例患者的中位随访时间为 5.6 个月(范围:1.1-14.2 个月)。无 PET/CT 显示病变、局限性疾病和任何远处转移(M1)的患者比例分别为 20%、43%和 37%。所有患者的 PET DR 为 80%。基于每位患者,复合队列中 F-rhPSMA-7 PET/CT 的 PPV 为 88%,CDR 为 70%。在组织病理学证实的队列中,PPV 为 91%,该亚组的 CDR 为 73%。PSA 水平≥1ng/mL 的患者 DR 和 PPV 分别为 90%和 91%,CDR 为 82%。PSA 水平<1ng/mL 的患者 DR 和 PPV 分别为 69%和 85%,CDR 为 59%。F-rhPSMA-7 PET/CT 的检测效果与分层 PSA 水平呈显著正相关(=0.005),与前列腺切除术后 PSA 最低点呈显著负相关(<0.001)。F-rhPSMA-7 PET/CT 在 RP 后 BCR 中提供高 PPV。其 CDR 取决于 PSCA 扫描前的值,PSA≥1ng/mL 的患者 CDR 非常好。