Department of Urology, Hospital Universitario Ramón y Cajal, IRYCIS, Universidad de Alcalá, Madrid, Spain.
Radiation Oncology Department, University Hospital Virgen del Rocío, Biomedical Institute of Seville (IBIS)/CSIC/University of Seville, Seville, Spain.
Clin Oncol (R Coll Radiol). 2023 Dec;35(12):e676-e688. doi: 10.1016/j.clon.2023.09.012. Epub 2023 Sep 27.
After primary radiotherapy, biochemical recurrence is defined according to the Phoenix criteria as a prostate-specific antigen (PSA) value >2 ng/ml relative to the nadir. Several studies have shown that prostate-specific membrane antigen (PSMA)-ligand positron emission tomography/computed tomography (PET/CT) can help in detecting recurrence in patients with low PSA values. This study aimed to assess the detection rate and patterns of PSMA-ligand PET/CT uptake in patients with suspected biochemical recurrence after primary radiotherapy and with PSA levels below the Phoenix threshold.
The meta-analysis was carried out in accordance with the Preferred Reporting Items for Systematic Reviews and Meta-Analyses statement. Articles providing data on patients with suspected prostate cancer recurrence after primary radiotherapy with a PSA value below the Phoenix threshold and who underwent PSMA-ligand PET/CT were included. Quality assessment was carried out using the Quality Assessment of Diagnostic Accuracy Studies-2 tool (QUADAS-2).
In total, five studies were included, recruiting 909 patients (202 with PSA ≤2 ng/ml). The PSMA-ligand detection rate in the patients with ≤2 ng/ml ranged from 66 to 83%. The most frequent source of PSMA-ligand PET/CT uptake was local recurrence, followed by lymph node metastasis and bone metastasis. PSMA-ligand PET/CT uptake due to local-only recurrence was more likely in patients with PSA ≤2 ng/ml compared with PSA > 2 ng/ml: risk ratio 0.72 (95% confidence interval 0.58-0.89), P = 0.003. No significant differences were observed in the detection of PSMA-ligand uptake in other areas. Limitations include a lack of biopsy confirmation, cohort reports with small sample sizes and a potentially high risk of bias.
A significant detection of PSMA-ligand-avid disease was observed in patients with PSA levels below the Phoenix threshold. There was a higher likelihood of detecting local-only uptake when the PSA value was ≤2 ng/ml. The findings suggest that a critical review of the Phoenix criteria may be warranted in the era of PSMA-ligand PET/CT and highlight the need for further prospective trials.
根据凤凰标准,原发性放疗后生化复发定义为前列腺特异性抗原(PSA)值相对于最低点 >2ng/ml。几项研究表明,前列腺特异性膜抗原(PSMA)-配体正电子发射断层扫描/计算机断层扫描(PET/CT)有助于检测 PSA 值较低的患者的复发。本研究旨在评估 PSMA-配体 PET/CT 在原发性放疗后疑似生化复发且 PSA 水平低于凤凰阈值的患者中的检测率和摄取模式。
该荟萃分析是按照系统评价和荟萃分析的首选报告项目进行的。纳入了提供原发性放疗后 PSA 值低于凤凰阈值且接受 PSMA-配体 PET/CT 检查的疑似前列腺癌复发患者数据的文章。使用诊断准确性研究质量评估-2 工具(QUADAS-2)进行质量评估。
共纳入 5 项研究,共纳入 909 例患者(PSA≤2ng/ml 患者 202 例)。PSA≤2ng/ml 患者的 PSMA-配体检测率为 66%至 83%。PSMA-配体 PET/CT 摄取最常见的来源是局部复发,其次是淋巴结转移和骨转移。与 PSA>2ng/ml 相比,PSA≤2ng/ml 患者的局部复发中 PSMA-配体摄取的可能性更高:风险比 0.72(95%置信区间 0.58-0.89),P=0.003。在其他区域检测到 PSMA-配体摄取没有显著差异。局限性包括缺乏活检证实、样本量小的队列报告和潜在的高偏倚风险。
在 PSA 水平低于凤凰阈值的患者中观察到 PSMA-配体活性疾病的显著检测。当 PSA 值≤2ng/ml 时,检测局部摄取的可能性更高。这些发现表明,在 PSMA-配体 PET/CT 时代,可能需要对凤凰标准进行严格审查,并强调需要进一步进行前瞻性试验。