超敏 PSA 预测根治性前列腺切除术后疾病进展的准确性。

IF 1.6 Q3 UROLOGY & NEPHROLOGY
BJUI compass Pub Date : 2024-09-15 DOI:10.1002/bco2.413
Heikki Seikkula, Jaakko Hyysalo, Mikael Högerman, Peter J. Boström, Otto Ettala
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引用次数: 0

摘要

研究目的评估前列腺癌根治术后超敏 PSA 值(usPSA)在预测后续生化复发(BCR)中的作用:研究纳入了2003年至2018年期间在图尔库大学医院接受开放式或机器人辅助前列腺癌根治术的1836名患者。排除标准包括接受辅助治疗的患者和未达到 PSA 最低值的患者(N = 1313)。我们为术后 3-5 年(N = 806)和随访 5 年以上(N = 493)的患者确定了最佳 usPSA 临界值。我们采用了曲线下面积(AUC)计算法和卡普兰-梅耶法:手术后首次监测时的uPSA阈值为0.01纳克/毫升(AUC = 0.80),是确定前列腺癌术后3年内低(80%)或高(20%)风险受试者的最佳临界值。除此以外,手术后前 3 年[(AUC = 0.89;手术后 3-5 年)和(AUC = 0.81;5 年后)]和 5 年(AUC = 0.85)的 uPSA 值在预测后续 BCR 方面优于 uPSA 最低值。值得注意的是,低uPSA nadir的EAU定义的高危患者保持了很高的无BCR生存率:总之,低uPSA可预测测量后2-3年内的最低BCR风险。在不影响疗效的情况下,低uPSA患者可以从减少手术后2-3年的PSA监测中获益。这种战略方法优化了繁忙的泌尿科门诊的资源分配,在芬兰这样的公费医疗系统中尤为重要。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

The accuracy of ultrasensitive PSA in predicting disease progression after radical prostatectomy

The accuracy of ultrasensitive PSA in predicting disease progression after radical prostatectomy

Objectives

To assess the role of ultrasensitive PSA values (usPSA) after radical prostatectomy in predicting the subsequent biochemical recurrence (BCR).

Material and methods

The study included 1836 patients who underwent open or robot-assisted RP at Turku University Hospital between 2003 and 2018. Exclusion criteria involved patients with adjuvant treatments and those who did not reach a PSA nadir <0.1 ng/ml, resulting in a final cohort of 1313 patients. The prognostic impact of the optimal usPSA nadir cut-off value 6 months after RP was investigated to predict subsequent BCR for the whole cohort (N = 1313). The optimal usPSA cut-off value was determined for patients at 3–5 years post-surgery (N = 806) and beyond 5 years (N = 493) of follow-up. We used the area under the curve (AUC) calculation and the Kaplan–Meier method.

Results

In a cohort with a median age of 64, primarily featuring Gleason score 7 prostate cancer. uPSA nadir of 0.01 ng/ml (AUC = 0.80) at the first monitoring post-surgery emerged as the optimal cut-off for identifying subjects at low (80%) or high (20%) risk of BCR within the first 3 years. Beyond this period, uPSA values during the first 3 [(AUC = 0.89; 3–5 years post-surgery) and (AUC = 0.81; beyond 5 years)] and 5 post-surgery years (AUC = 0.85) outperformed uPSA nadir in predicting subsequent BCR. Notably, EAU-defined high-risk patients with low uPSA nadir maintained substantial BCR-free survival.

Conclusion

In conclusion, a low usPSA predicts minimal BCR risk over the next 2–3 years post-measurement. Patients with low usPSA can benefit from reduced post-surgery PSA monitoring at 2- to 3-year intervals without compromising outcomes. This strategic approach optimizes resource allocation in busy urological outpatient clinics, especially valuable in publicly reimbursed healthcare systems like Finland.

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CiteScore
2.30
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