Carver Brett S, Bozeman Caleb B, Simoneaux Walter J, Venable Dennis D, Kattan Michael W, Eastham James A
Department of Urology, Louisiana State University-Health Sciences Center and Overton Brooks Veterans Administration Medical Center, Shreveport, Louisiana, USA.
J Urol. 2004 Nov;172(5 Pt 1):1853-5. doi: 10.1097/01.ju.0000141248.28904.fd.
We evaluated men undergoing repeat prostate biopsies for persistently increased serum prostate specific antigen (PSA) levels to determine if race was a predictor of cancer detection.
Between July 1995 and June 2002, 401 men had undergone 2 or more transrectal ultrasound guided prostate biopsies at our institutions. Clinical information was gathered using our prostate biopsy database and retrospectively reviewed. Race, age, serum PSA, PSA velocity, total number of biopsies performed, total number of previous negative cores and the presence of high grade prostatic intraepithelial neoplasia (HGPIN) or atypical small acinar proliferation (ASAP) on prior biopsy were evaluated to determine if they were predictors of subsequent cancer detection. Multivariate analysis was performed using a time dependent covariate Cox proportional hazards model.
Of the 401 men undergoing repeat prostate biopsy, 91 (22.7%) were diagnosed with prostate cancer. In total there were 180 (44.9%) black men and 221 (55.1%) white men. Cancer was diagnosed in 49 black men (27.2%) and 42 white men (19.0%, p = 0.06). On multivariate analysis serum PSA, HGPIN, ASAP and PSA velocity were predictors of prostate cancer detection (p = 0.006, <0.0001, 0.001 and 0.0004, respectively). Race was not found to be a predictor of prostate cancer detection on repeat prostate biopsy (p = 0.16). In the evaluation of clinical data for racial differences, black men had a significantly higher incidence of HGPIN on prior biopsy compared to white men (p = 0.02). Serum PSA, PSA velocity, presence of ASAP on prior biopsy, age, number of biopsies performed and number of previous negative cores were not statistically different between black and white men.
Race is not a predictor of prostate cancer detection in men undergoing repeat prostate biopsies. With the exception of HGPIN, all other clinical parameters were similar between black and white men. Serum PSA, PSA velocity, HGPIN and ASAP were found to be significant predictors of subsequent prostate cancer detection.
我们对因血清前列腺特异性抗原(PSA)水平持续升高而接受重复前列腺活检的男性进行评估,以确定种族是否为癌症检测的预测因素。
1995年7月至2002年6月期间,401名男性在我们机构接受了2次或更多次经直肠超声引导下的前列腺活检。使用我们的前列腺活检数据库收集临床信息并进行回顾性分析。评估种族、年龄、血清PSA、PSA变化率、活检总次数、既往阴性活检样本总数以及既往活检中高级别前列腺上皮内瘤变(HGPIN)或非典型小腺泡增生(ASAP)的存在情况,以确定它们是否为后续癌症检测的预测因素。使用时间依赖性协变量Cox比例风险模型进行多变量分析。
在401名接受重复前列腺活检的男性中,91名(22.7%)被诊断为前列腺癌。总共有180名(44.9%)黑人男性和221名(55.1%)白人男性。49名黑人男性(27.2%)和42名白人男性(19.0%,p = 0.06)被诊断为癌症。多变量分析显示,血清PSA、HGPIN、ASAP和PSA变化率是前列腺癌检测的预测因素(p分别为0.006、<0.0001、0.001和0.0004)。在重复前列腺活检中,未发现种族是前列腺癌检测的预测因素(p = 0.16)。在评估种族差异的临床数据时,黑人男性既往活检中HGPIN的发生率显著高于白人男性(p = 0.02)。黑人男性和白人男性之间的血清PSA、PSA变化率、既往活检中ASAP的存在情况、年龄、活检次数和既往阴性活检样本总数在统计学上无差异。
在接受重复前列腺活检的男性中,种族不是前列腺癌检测的预测因素。除HGPIN外,黑人男性和白人男性的所有其他临床参数相似。血清PSA、PSA变化率、HGPIN和ASAP被发现是后续前列腺癌检测的重要预测因素。