Bruno J James, Armenakas Noel A, Fracchia John A
Department of Surgery, Division of Urology, Lenox Hill Hospital, New York, New York 10021, USA.
J Urol. 2007 May;177(5):1741-4. doi: 10.1016/j.juro.2007.01.067.
Percent free prostate specific antigen and prostate specific antigen density have been independently shown to increase the specificity of prostate cancer screening in men with prostate specific antigen levels between 4.1 and 10.0 ng/ml. Recent data suggest the total prostate specific antigen cutoff for performing a biopsy should be 2.6 ng/ml. We assessed the influence of percent free prostate specific antigen and prostate volume on cancer detection in men with a prostate specific antigen between 2.6 and 10.0 ng/ml.
From 1991 to 2005 all transrectal ultrasound guided prostate biopsies (5,587) for abnormal digital rectal examination and/or increased age specific prostate specific antigen were evaluated. A total of 1,072 patients with a prostate specific antigen between 2.6 and 10.0 ng/ml and any percent free prostate specific antigen were included in study. The cancer detection rate was calculated for each percent free prostate specific antigen/volume stratum.
Prostate cancer was detected in 296 patients (27.6%). The mean age and prostate specific antigen of the patients with benign pathology and prostate cancer were similar. Mean percent free prostate specific antigen was 17.5% and 14.1% (p>0.05), and the mean volume was 62.0 and 46.0 cc (p=0.001), respectively. The strongest risk factors for a positive biopsy were percent free prostate specific antigen (odds ratio 0.004, p<0.001), volume (OR 0.977, p<0.001) and digital rectal examination (OR 1.765, p=0.007), but not total prostate specific antigen (p=0.303). When stratified by volume and percent free prostate specific antigen, distinct risk groups were identified. The probability of detecting cancer inversely correlated with prostate volume and percent free prostate specific antigen.
In men with prostate specific antigen levels between 2.6 and 10.0 ng/ml, the probability of detecting cancer was inversely proportional to prostate volume and percent free prostate specific antigen. This table may assist in predicting patient risk for harboring prostate cancer.
游离前列腺特异性抗原百分比和前列腺特异性抗原密度已被独立证明可提高前列腺特异性抗原水平在4.1至10.0 ng/ml之间男性前列腺癌筛查的特异性。近期数据表明,进行活检的总前列腺特异性抗原临界值应为2.6 ng/ml。我们评估了游离前列腺特异性抗原百分比和前列腺体积对前列腺特异性抗原在2.6至10.0 ng/ml之间男性癌症检测的影响。
对1991年至2005年期间因直肠指检异常和/或年龄特异性前列腺特异性抗原升高而进行的所有经直肠超声引导下前列腺活检(5587例)进行评估。共有1072例前列腺特异性抗原在2.6至10.0 ng/ml之间且有任何游离前列腺特异性抗原百分比的患者纳入研究。计算每个游离前列腺特异性抗原/体积分层的癌症检测率。
296例患者(27.6%)检测出前列腺癌。良性病理和前列腺癌患者的平均年龄和前列腺特异性抗原相似。游离前列腺特异性抗原平均百分比分别为17.5%和14.1%(p>0.05),平均体积分别为62.0和46.0 cc(p=0.001)。活检阳性的最强危险因素是游离前列腺特异性抗原百分比(比值比0.004,p<0.001)、体积(OR 0.977,p<0.001)和直肠指检(OR 1.765,p=0.007),而非总前列腺特异性抗原(p=0.303)。按体积和游离前列腺特异性抗原百分比分层时,确定了不同的风险组。检测到癌症的概率与前列腺体积和游离前列腺特异性抗原百分比呈负相关。
在前列腺特异性抗原水平在2.6至10.0 ng/ml之间的男性中,检测到癌症的概率与前列腺体积和游离前列腺特异性抗原百分比成反比。此表可能有助于预测患者患前列腺癌的风险。