Irani J, Millet C, Levillain P, Doré B, Begon F, Aubert J
Departments of Urology, Nuclear Medicine and Pathology, Centre Hospitalier Universitaire, La Milétrie, Poitiers, France.
J Urol. 1997 Jan;157(1):185-8. doi: 10.1016/s0022-5347(01)65319-9.
Benign prostatic hyperplasia (BPH) was shown to be associated with high concentrations of urinary prostate specific antigen (PSA). We investigated the serum-to-urinary PSA ratio in patients undergoing prostate biopsy to assess its efficacy in enhancing serum PSA specificity in the detection of prostate carcinoma.
From November 1995 through January 1996 consecutive patients undergoing prostate biopsy were prospectively included in the study. Serum and urine PSA levels were measured at our laboratory with the Tandem-R assay. Samples were drawn 24 hours before prostate biopsy and at a distance from prostatic manipulation or ejaculation.
We studied 73 patients with BPH and 57 with prostate cancer. Differences between BPH and prostate cancer were statistically significant considering serum PSA or serum-to-urinary PSA ratios. In the 50 patients with a serum PSA of 4.0 to 10.0 ng./ml. (35 with BPH and 15 with prostate cancer) the differences between prostate cancer and BPH were still significant only when considering serum-to-urinary PSA ratio. Receiver operating characteristic curves showed that serum-to-urinary PSA ratio was a better predictor of prostate cancer than serum PSA.
Our results suggest that the serum-to-urinary PSA ratio may be useful in distinguishing BPH from prostate cancer, particularly in the diagnostic gray zone of serum PSA between 4.0 and 10.0 ng./ml.
研究表明良性前列腺增生(BPH)与高浓度的尿前列腺特异性抗原(PSA)相关。我们调查了接受前列腺活检患者的血清与尿液PSA比值,以评估其在提高血清PSA检测前列腺癌特异性方面的效果。
从1995年11月至1996年1月,连续接受前列腺活检的患者被前瞻性纳入本研究。血清和尿液PSA水平在我们实验室采用串联R法进行测量。样本在前列腺活检前24小时采集,且采集时远离前列腺操作或射精。
我们研究了73例BPH患者和57例前列腺癌患者。考虑血清PSA或血清与尿液PSA比值时,BPH和前列腺癌之间的差异具有统计学意义。在血清PSA为4.0至10.0 ng./ml的50例患者中(35例BPH患者和15例前列腺癌患者),仅考虑血清与尿液PSA比值时,前列腺癌和BPH之间的差异仍然显著。受试者工作特征曲线显示,血清与尿液PSA比值比血清PSA能更好地预测前列腺癌。
我们的结果表明,血清与尿液PSA比值可能有助于区分BPH和前列腺癌,特别是在血清PSA处于4.0至10.0 ng./ml的诊断灰色区域时。