Department of Urology, Charité University Medicine, Berlin, Germany.
J Urol. 2012 Dec;188(6):2165-70. doi: 10.1016/j.juro.2012.07.106. Epub 2012 Oct 18.
Limited data exist on the relationship of percent free prostate specific antigen and prostate specific antigen density with prostate cancer prognosis. Therefore, we compared percent free prostate specific antigen and prostate specific antigen density with prostate specific antigen, Gleason sum and stage to predict prostate cancer prognosis in a large cohort using a single prostate specific antigen and free prostate specific antigen assay.
Between 1999 and 2007 a total of 1,656 patients with prostate cancer underwent laparoscopic radical prostatectomy at the Charité Berlin. There were 322 patients excluded from analysis for a variety of reasons. The final 1,334 patients had prostate specific antigen, free prostate specific antigen, prostate volume and complete pathological analysis available.
Median followup was 60.3 months (range 0.2 to 135). Median age (63 years, range 43 to 75) did not differ between the 1,092 patients without and the 242 with biochemical recurrence (p = 0.956), but prostate volume, prostate specific antigen and percent free prostate specific antigen differed significantly (p <0.0001). While prostate specific antigen and prostate specific antigen density increased significantly in patients with Gleason less than 7, 7 and greater than 7 tumors, percent free prostate specific antigen decreased significantly (p <0.0001). Prostate specific antigen, percent free prostate specific antigen and prostate specific antigen density differed significantly between pT2 and pT3 tumors, and between patients with vs without positive surgical margins. On univariate analysis Gleason sum, pathological stage, positive surgical margin, total prostate specific antigen, percent free prostate specific antigen and prostate specific antigen density were predictors of biochemical recurrence-free survival. Multivariate Cox regression analysis identified Gleason sum, pathological stage, positive surgical margin and prostate specific antigen density as independent predictors of biochemical recurrence-free survival, while percent free prostate specific antigen and total prostate specific antigen failed to be significant.
Few models for prostate cancer prognosis include prostate specific antigen density. There is substantial value in prostate specific antigen density but not in percent free prostate specific antigen for improving prostate cancer prognosis and biochemical recurrence prediction.
关于游离前列腺特异性抗原(PSA)百分比和 PSA 密度与前列腺癌预后的关系,目前仅有少量数据。因此,我们通过单一的 PSA 和游离 PSA 检测,在一个大的队列中比较了游离 PSA 百分比和 PSA 密度与 PSA、Gleason 总和及分期,以预测前列腺癌的预后。
1999 年至 2007 年间,共有 1656 例前列腺癌患者在柏林 Charité 接受腹腔镜根治性前列腺切除术。由于各种原因,有 322 例患者被排除在分析之外。最终有 1334 例患者有 PSA、游离 PSA、前列腺体积和完整的病理分析结果。
中位随访时间为 60.3 个月(范围 0.2 至 135)。1092 例无生化复发患者和 242 例生化复发患者的中位年龄(63 岁,范围 43 至 75)无差异(p=0.956),但前列腺体积、PSA 和游离 PSA 百分比差异有统计学意义(p<0.0001)。在 Gleason 评分<7、7 和>7 肿瘤患者中,PSA 和 PSA 密度显著升高,而游离 PSA 百分比显著降低(p<0.0001)。在 pT2 和 pT3 肿瘤患者之间,以及在有和无阳性切缘的患者之间,PSA、游离 PSA 百分比和 PSA 密度均有显著差异。在单因素分析中,Gleason 总和、病理分期、阳性切缘、总 PSA、游离 PSA 百分比和 PSA 密度是生化无复发生存的预测因子。多因素 Cox 回归分析确定 Gleason 总和、病理分期、阳性切缘和 PSA 密度是生化无复发生存的独立预测因子,而游离 PSA 百分比和总 PSA 无统计学意义。
少数前列腺癌预后模型包括 PSA 密度。PSA 密度对改善前列腺癌预后和生化复发预测具有重要价值,而游离 PSA 百分比则没有价值。