Division of Urologic Surgery, Department of Surgery, and the Duke Prostate Center, Durham, NC, USA.
BJU Int. 2010 Jun;105(11):1541-7. doi: 10.1111/j.1464-410X.2009.09016.x. Epub 2009 Nov 12.
To define a level of persistently elevated prostate-specific antigen (PSA) after radical prostatectomy (RP) that equates with high-risk for disease progression, and to identify preoperative predictors of PSA persistence among men from the Shared Equal Access Regional Cancer Hospital (SEARCH) database.
A total of 901 men treated with RP between 2001 and 2008 were separated into groups based upon PSA nadir within 6 months after RP. We explored the association between nadir groups and time to biochemical recurrence (BCR) using multivariate Cox proportional hazards and determined the preoperative predictors of PSA persistence using logistic regression.
Relative to men with undetectable PSA levels, those with a PSA nadir of 0.03 (hazard ratio [HR] 3.88, P < 0.001), 0.04 (HR 4.87, P < 0.001), 0.05-0.09 (HR 12.69, P < 0.001), 0.1-0.19 (HR 13.17, P < 0.001), and 0.2 ng/mL (HR 13.23, P < 0.001) were at increased risk of BCR while men with a nadir of 0.01 (HR 1.36, P = 0.400) and 0.02 (HR 1.64, P = 0.180) were not. Using the PSA persistence definition of a PSA nadir > or = 0.03 ng/mL, 230 men (26%) had persistence. The independent preoperative predictors of PSA persistence were higher body mass index (BMI, P = 0.002), pathological Gleason score (relative to 2-6: 4 + 3-10, P = 0.001) and preoperative PSA level (P < 0.001).
Men with a PSA nadir > or = 0.03 ng/mL after RP were at higher risk for BCR. Using a PSA persistence definition of a PSA nadir > or = 0.03 ng/mL, persistence was predicted by known factors associated with aggressive disease (tumour grade, PSA level and BMI). Validation of the present definition in different populations using later end-points remains necessary to assess its prognostic usefulness.
定义根治性前列腺切除术(RP)后持续升高的前列腺特异性抗原(PSA)水平,使其等同于疾病进展的高危水平,并确定 SEARCH 数据库中男性 RP 术后 PSA 持续存在的术前预测因子。
将 2001 年至 2008 年间接受 RP 治疗的 901 名男性根据 RP 后 6 个月内 PSA 最低点分为几组。我们使用多变量 Cox 比例风险模型探讨最低点组与生化复发(BCR)时间之间的关系,并使用逻辑回归确定 PSA 持续存在的术前预测因子。
与 PSA 水平无法检测到的男性相比,PSA 最低点为 0.03(危险比 [HR] 3.88,P < 0.001)、0.04(HR 4.87,P < 0.001)、0.05-0.09(HR 12.69,P < 0.001)、0.1-0.19(HR 13.17,P < 0.001)和 0.2 ng/mL(HR 13.23,P < 0.001)的男性发生 BCR 的风险增加,而 PSA 最低点为 0.01(HR 1.36,P = 0.400)和 0.02(HR 1.64,P = 0.180)的男性则没有。使用 PSA 持续存在的 PSA 最低点定义为 > 或 = 0.03 ng/mL,有 230 名男性(26%)存在持续存在。PSA 持续存在的独立术前预测因子为较高的体重指数(BMI,P = 0.002)、病理 Gleason 评分(与 2-6 分相比:4 + 3-10,P = 0.001)和术前 PSA 水平(P < 0.001)。
RP 后 PSA 最低点 > 或 = 0.03 ng/mL 的男性发生 BCR 的风险更高。使用 PSA 最低点定义为 > 或 = 0.03 ng/mL 的 PSA 持续存在,持续性由与侵袭性疾病相关的已知因素(肿瘤分级、PSA 水平和 BMI)预测。使用不同人群的后期终点验证本定义以评估其预后价值仍然是必要的。