New York University School of Medicine, New York, NY, USA.
Eur Urol. 2011 Sep;60(3):548-53. doi: 10.1016/j.eururo.2011.05.036. Epub 2011 May 26.
Prostate-specific antigen (PSA) is the only independent predictor of biochemical recurrence (BCR) following radical prostatectomy (RP) subject to change over time.
To determine whether an ultrasensitive PSA measured at 3 yr following RP is a predictor of subsequent BCR.
DESIGN, SETTING, AND PARTICIPANTS: There were 1197 consecutive men with clinically localized prostate cancer who underwent an open radical retropubic prostatectomy (ORRP) at a tertiary referral academic medical center. Exclusions included 107 men (8.9%) who developed a PSA level ≥ 0.2 ng/ml or underwent hormone therapy or radiation therapy (RT) within the first 3 r after surgery, 191 men (16%) who did not undergo a 3-yr ultrasensitive PSA assay, and 98 men (8.2%) who had PSA levels ≥ 0.1 and <0.2 at 3 yr. The remaining 801 men were stratified into two groups based on their ultrasensitive PSA level at 3 yr postoperatively: group 1, which consisted of patients whose PSA was ≤ 0.04 (n = 765), and group 2, which consisted of patients whose PSA was >0.04 and <0.10 (n = 36).
Delayed BCR was the primary end point and represented those men in this cohort who developed a PSA level ≥ 0.2 or underwent salvage RT for a persistently rising PSA level after 3 yr of follow-up.
The 7-yr cumulative BCR-free survival rate for groups 1 and 2 was 0.957 (95% confidence interval [CI], 0.920-0.978) and 0.654 (95% CI, 0.318-0.855), respectively. In multivariable Cox proportional hazards models, ultrasensitive PSA level at 3 yr remained the only significant predictor of delayed BCR (likelihood ratio χ(2) for full model: 27.03; df = 1; p < 0.001). A limitation of the study is that no uniform PSA assay was obtained.
Our findings provide compelling evidence that an ultrasensitive PSA at 3 yr following RP provides useful insights into delayed BCR and is a source of reassurance for the overwhelming majority of men being followed for delayed recurrences.
前列腺特异性抗原(PSA)是根治性前列腺切除术(RP)后生化复发(BCR)的唯一独立预测因子,但会随时间变化。
确定 RP 后 3 年测量的超敏 PSA 是否可预测随后的 BCR。
设计、地点和参与者:共有 1197 例连续的局限性前列腺癌男性患者在一家三级转诊学术医疗中心接受开放式经直肠前列腺根治切除术(ORRP)。排除标准包括 107 例(8.9%)患者在手术后 3 年内 PSA 水平≥0.2ng/ml 或接受激素治疗或放射治疗(RT),191 例(16%)未行 3 年超敏 PSA 检测,98 例(8.2%)患者在 3 年时 PSA 水平≥0.1 且 <0.2ng/ml。其余 801 例患者根据术后 3 年超敏 PSA 水平分为两组:组 1,PSA 水平≤0.04(n=765);组 2,PSA 水平>0.04 且 <0.10(n=36)。
延迟 BCR 为主要终点,代表该队列中在随访 3 年后 PSA 水平≥0.2 或因 PSA 持续升高而行挽救性 RT 的患者。
组 1 和组 2 的 7 年无 BCR 累积生存率分别为 0.957(95%置信区间[CI],0.920-0.978)和 0.654(95%CI,0.318-0.855)。在多变量 Cox 比例风险模型中,术后 3 年的超敏 PSA 水平仍然是延迟 BCR 的唯一显著预测因素(全模型似然比 χ(2)检验:27.03;df=1;p<0.001)。该研究的局限性在于未获得统一的 PSA 检测。
我们的研究结果提供了有力的证据,表明 RP 后 3 年的超敏 PSA 能深入了解延迟 BCR,并为绝大多数接受延迟复发随访的男性提供了安心的依据。