Bolduc Stéphane, Lacombe Louis, Naud Alain, Grégoire Mireille, Fradet Yves, Tremblay Roland R
Division of Urology, Centre Hospitalier Universitaire de Québec (CHUQ), Laval University, Québec, Que.
Can Urol Assoc J. 2007 Nov;1(4):377-81. doi: 10.5489/cuaj.444.
Our objective was to evaluate the usefulness of urinary prostate specific antigen (PSA) in the differential diagnosis of benign prostatic hyperplasia (BPH) and prostate cancer.
We undertook a prospective study and obtained informed consent from 170 men. They provided blood samples to measure serum PSA and 50 mL of first-voided urine to measure urinary PSA. Seventy-seven men were diagnosed with BPH; 42 patients had newly diagnosed prostate cancer; and 51 were selected as age-matched control subjects. Data were analyzed using Wilcoxon signed rank tests, receiver operating characteristic (ROC) curves and logistic regression.
Prostate volume was 35 cm(3) and 45 cm(3) (p < 0.05), serum PSA was 9.7 ng/mL and 4.5 ng/mL (p < 0.001) and PSA density was 0.28 and 0.11 (p < 0.01) for prostate cancer and BPH patients, respectively. Overall, urinary PSA was not significantly different, but PSA ratio (urinary:serum) was significantly different at 6.7 and 30.6 (p < 0.001) for prostate cancer and BPH patients, respectively. A subgroup with serum PSA between 2.5 ng/mL and 10.0 ng/mL was selected and urinary PSA was significant: 52.6 ng/mL (n = 29) and 123.2 ng/mL (n = 35) (p < 0.05) for prostate cancer and BPH patients, respectively. PSA ratios were also significant (p = 0.007). ROC curves identified a cutoff for urinary PSA at > 150 ng/mL, with a sensitivity of 92.5%. When comparing prostate cancer patients with age-matched control subjects, serum PSA, urinary PSA and PSA ratio were different (p = 0.004).
Our study supports urinary PSA as a useful marker in the differential diagnosis of prostate cancer and BPH, especially when serum PSA is between 2.5 ng/mL and 10 ng/mL. Low urinary PSA and PSA ratios point toward prostate cancer. A urinary PSA threshold of > 150 ng/mL may be used to decrease the number of prostatic biopsies.
我们的目的是评估尿前列腺特异性抗原(PSA)在良性前列腺增生(BPH)和前列腺癌鉴别诊断中的作用。
我们进行了一项前瞻性研究,并获得了170名男性的知情同意。他们提供血样以检测血清PSA,并提供50毫升首次晨尿以检测尿PSA。77名男性被诊断为BPH;42例患者为新诊断的前列腺癌;51名被选为年龄匹配的对照受试者。数据采用Wilcoxon符号秩检验、受试者工作特征(ROC)曲线和逻辑回归进行分析。
前列腺癌患者和BPH患者的前列腺体积分别为35立方厘米和45立方厘米(p<0.05),血清PSA分别为9.7纳克/毫升和4.5纳克/毫升(p<0.001),PSA密度分别为0.28和0.11(p<0.01)。总体而言,尿PSA无显著差异,但前列腺癌患者和BPH患者的PSA比值(尿:血清)有显著差异,分别为6.7和30.6(p<0.001)。选择血清PSA在2.5纳克/毫升至10.0纳克/毫升之间的一个亚组,尿PSA有显著差异:前列腺癌患者和BPH患者分别为52.6纳克/毫升(n=29)和123.2纳克/毫升(n=35)(p<0.05)。PSA比值也有显著差异(p=0.007)。ROC曲线确定尿PSA的临界值>150纳克/毫升,敏感性为92.5%。当将前列腺癌患者与年龄匹配的对照受试者进行比较时,血清PSA、尿PSA和PSA比值存在差异(p=0.004)。
我们的研究支持尿PSA作为前列腺癌和BPH鉴别诊断中的一个有用标志物,尤其是当血清PSA在2.5纳克/毫升至10纳克/毫升之间时。低尿PSA和PSA比值提示前列腺癌。尿PSA阈值>150纳克/毫升可用于减少前列腺活检的数量。