根治性前列腺切除术后生化复发患者的游离总 PSA 比率与 18F-DCFPyL 前列腺特异性膜抗原 PET/CT 发现的关联:一项前瞻性单中心研究

Rui M. Bernardino, Katherine Lajkosz, Leyi B. Yin, Rashid K. Sayyid, Marian Wettstein, Harkanwal Randhawa, Jessica G. Cockburn, Sayeed Ahmed, Rosita Thomassian, Eleftherios Diamandis, Ur Metser, Alejandro Berlin, Neil E. Fleshner
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Our aim in this study was to determine the association of FPSAR in patients referred for <sup>18</sup>F-DCFPyL PSMA PET/CT in the BCR setting and assess the correlation between FPSAR and <sup>18</sup>F-DCFPyL PSMA PET/CT positivity (local recurrence or distant metastases). <strong>Methods:</strong> This prospective study included 137 patients who were referred for <sup>18</sup>F-DCFPyL PSMA PET/CT and had BCR with a total PSA of less than 1 ng/mL after radical prostatectomy (RP) (including adjuvant or salvage radiotherapy). Blood samples were collected on the day of <sup>18</sup>F-DCFPyL PSMA PET/CT. FPSAR was categorized as less than 0.10 or as 0.10 or more. A positive <sup>18</sup>F-DCFPyL PSMA PET/CT scan was defined by a PROMISE classification lesion score of 2 or 3, irrespective of the site of increased tracer uptake (e.g., prostate, pelvic nodes, bone, or viscera). <strong>Results:</strong> Overall, 137 blood samples of patients with BCR after RP were analyzed to calculate FPSAR. The median age at <sup>18</sup>F-DCFPyL PSMA PET/CT was 68.6 y (interquartile range, 63.0–72.4 y), and the median PSA at <sup>18</sup>F-DCFPyL PSMA PET/CT was 0.3 ng/mL (interquartile range, 0.3–0.6 ng/mL). Eighty-six patients (62.8%) had an FPSAR of less than 0.10, whereas 51 patients (37.2%) had an FPSAR of 10 or more. 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引用次数: 0

摘要

在加拿大和全球各地,PSMA PET/CT 的使用机会有限且费用昂贵。对于前列腺癌治疗后生化复发(BCR)的患者,需要采用新的策略来更好地对可能或不可能从 PSMA PET 扫描中获益的患者进行分层。游离前列腺特异性抗原(PSA)与总前列腺特异性抗原(PSA)的比值(FPSAR)在前列腺癌治疗后的作用,特别是在 PSMA PET/CT 时代的作用仍不清楚。本研究旨在确定在 BCR 环境下转诊接受 18F-DCFPyL PSMA PET/CT 的患者中 FPSAR 的相关性,并评估 FPSAR 与 18F-DCFPyL PSMA PET/CT 阳性(局部复发或远处转移)之间的相关性。研究方法这项前瞻性研究纳入了137名转诊接受18F-DCFPyL PSMA PET/CT检查的患者,这些患者在接受根治性前列腺切除术(RP)(包括辅助或挽救性放疗)后出现BCR,总PSA小于1 ng/mL。血液样本在 18F-DCFPyL PSMA PET/CT 当天采集。FPSAR分为小于0.10和大于0.10两种。18F-DCFPyL PSMA PET/CT 扫描阳性的定义是 PROMISE 分类病变评分为 2 或 3,而不论示踪剂摄取增加的部位(如前列腺、盆腔结节、骨或内脏)。结果共分析了 137 例 RP 后 BCR 患者的血液样本,以计算 FPSAR。18F-DCFPyL PSMA PET/CT 时的中位年龄为 68.6 岁(四分位间范围为 63.0-72.4 岁),18F-DCFPyL PSMA PET/CT 时的中位 PSA 为 0.3 纳克/毫升(四分位间范围为 0.3-0.6 纳克/毫升)。86名患者(62.8%)的FPSAR小于0.10,而51名患者(37.2%)的FPSAR达到或超过10。FPSAR大于或等于10被认为是18F-DCFPyL PSMA PET/CT扫描阳性的独立预测因素,其几率比为6.99(95% CI,2.96-16.51;P< 0.001)。结论RP术后FPSAR达到或超过10与BCR术后RP患者18F-DCFPyL PSMA PET/CT扫描阳性几率增加独立相关。这些发现可能提供了一种廉价的方法,可用于在可用性不充分的地区对 18F-DCFPyL PSMA PET/CT 进行分流。
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Association of Free-to-Total PSA Ratio and 18F-DCFPyL Prostate-Specific Membrane Antigen PET/CT Findings in Patients with Biochemical Recurrence After Radical Prostatectomy: A Prospective Single-Center Study

In Canada and across the globe, access to PSMA PET/CT is limited and expensive. For patients with biochemical recurrence (BCR) after treatment for prostate cancer, novel strategies are needed to better stratify patients who may or may not benefit from a PSMA PET scan. The role of the free-to-total prostate-specific antigen (PSA) ratio (FPSAR) in posttreatment prostate cancer, specifically in the PSMA PET/CT era, remains unknown. Our aim in this study was to determine the association of FPSAR in patients referred for 18F-DCFPyL PSMA PET/CT in the BCR setting and assess the correlation between FPSAR and 18F-DCFPyL PSMA PET/CT positivity (local recurrence or distant metastases). Methods: This prospective study included 137 patients who were referred for 18F-DCFPyL PSMA PET/CT and had BCR with a total PSA of less than 1 ng/mL after radical prostatectomy (RP) (including adjuvant or salvage radiotherapy). Blood samples were collected on the day of 18F-DCFPyL PSMA PET/CT. FPSAR was categorized as less than 0.10 or as 0.10 or more. A positive 18F-DCFPyL PSMA PET/CT scan was defined by a PROMISE classification lesion score of 2 or 3, irrespective of the site of increased tracer uptake (e.g., prostate, pelvic nodes, bone, or viscera). Results: Overall, 137 blood samples of patients with BCR after RP were analyzed to calculate FPSAR. The median age at 18F-DCFPyL PSMA PET/CT was 68.6 y (interquartile range, 63.0–72.4 y), and the median PSA at 18F-DCFPyL PSMA PET/CT was 0.3 ng/mL (interquartile range, 0.3–0.6 ng/mL). Eighty-six patients (62.8%) had an FPSAR of less than 0.10, whereas 51 patients (37.2%) had an FPSAR of 10 or more. An FPSAR of 10 or more was identified as an independent predictor of a positive 18F-DCFPyL PSMA PET/CT scan, with an odds ratio of 6.99 (95% CI, 2.96–16.51; P < 0.001). Conclusion: An FPSAR of 10 or more after RP independently correlated with increased odds of a positive 18F-DCFPyL PSMA PET/CT scan among BCR post-RP patients. These findings may offer an inexpensive method by which to triage access to 18F-DCFPyL PSMA PET/CT in jurisdictions where availability is not replete.

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