Yanke Brent V, Salzhauer Elan W, Colon Ivan
Department of Urology, State University of New York Downstate School of Medicine, 445 Lenox Road, Brooklyn, NY 11203, USA.
J Urol. 2006 Sep;176(3):1114-7. doi: 10.1016/j.juro.2006.04.041.
High grade intraepithelial neoplasia and atypical small acinar proliferation increase the probability of cancer on a subsequent prostate biopsy. We investigated whether race is prognostic for detecting cancer in patients undergoing repeat prostate biopsies.
At a single institution 416 men underwent 2 or more prostate biopsies from January 1993 through June 2003 for a total of 1,023 biopsies. We retrospectively examined multiple factors, including patient age, race, total number of biopsy cores total number of previously negative biopsy cores, prostate specific antigen, prostate specific antigen slope, digital rectal examination and family history of prostate cancer. Previous high grade intraepithelial neoplasia, atypical small acinar proliferation and Gleason score in positive biopsies were recorded from the histopathology review. Clinical variables were compared between black and white men using the Wilcoxon rank sum and Fisher exact tests. The Cox proportional hazards model was used for multivariate analysis.
Of the 416 men 216 (51.9%) were black, 174 (41.8%) were white and 26 (6.3%) were another race. The average number of biopsy sessions in black and white men was 2.41 and 2.51, respectively. The cancer detection rate was 35.1% at the second biopsy, 34.6% at the third biopsy and 32.0% at the fourth biopsy. Cancer was diagnosed in 43.5% of black men compared to 25.9% of white men (p = 0.0004). When clinical and pathological variables were compared between the racial groups, black men had significantly higher prostate specific antigen (p = 0.02). There was no statistically significant difference in patient age, total number of cores, number of previous negative cores, prostate specific antigen slope, abnormal digital rectal examination, family history, or previous high grade intraepithelial neoplasia or atypical small acinar proliferation. Multivariate analysis showed that race approached but did not achieve statistical significance as a predictor of prostate cancer on repeat biopsy (p = 0.09). Previous high grade intraepithelial neoplasia (p = 0.0025), previous atypical small acinar proliferation (p = 0.0049), digital rectal examination (p = 0.0076) and prostate specific antigen slope (p = 0.0005) were independent predictors of prostate cancer on repeat biopsy. Of patients with previous atypical small acinar proliferation black men had a significantly higher rate of cancer detection on repeat biopsy.
Previous high grade intraepithelial neoplasia, atypical small acinar proliferation, digital rectal examination and prostate specific antigen slope were independent predictors of prostate cancer on repeat biopsy. Race approached but did not attain significance after adjusting for disease features.
高级别上皮内瘤变和非典型小腺泡增生会增加后续前列腺活检时患癌的可能性。我们研究了种族因素对于接受重复前列腺活检患者癌症检测是否具有预后意义。
在一家机构中,从1993年1月至2003年6月,416名男性接受了2次或更多次前列腺活检,共计1023次活检。我们回顾性检查了多个因素,包括患者年龄、种族、活检芯针总数、既往阴性活检芯针总数、前列腺特异性抗原、前列腺特异性抗原斜率、直肠指检以及前列腺癌家族史。从组织病理学检查记录中获取既往阳性活检中的高级别上皮内瘤变、非典型小腺泡增生以及Gleason评分。使用Wilcoxon秩和检验和Fisher精确检验比较黑人和白人男性之间的临床变量。采用Cox比例风险模型进行多变量分析。
416名男性中,216名(51.9%)为黑人,174名(41.8%)为白人,26名(6.3%)为其他种族。黑人和白人男性的平均活检次数分别为2.41次和2.51次。第二次活检时癌症检出率为35.1%,第三次活检时为34.6%,第四次活检时为32.0%。43.5%的黑人男性被诊断出患有癌症,而白人男性为25.9%(p = 0.0004)。当比较不同种族组之间的临床和病理变量时,黑人男性的前列腺特异性抗原显著更高(p = 0.02)。在患者年龄、芯针总数、既往阴性芯针数、前列腺特异性抗原斜率、直肠指检异常、家族史或既往高级别上皮内瘤变或非典型小腺泡增生方面,没有统计学上的显著差异。多变量分析显示,种族因素在重复活检中作为前列腺癌的预测指标接近但未达到统计学意义(p = 0.09)。既往高级别上皮内瘤变(p = 0.0025)、既往非典型小腺泡增生(p = 0.0049)、直肠指检(p = 0.0076)和前列腺特异性抗原斜率(p = 0.0005)是重复活检中前列腺癌的独立预测指标。在既往有非典型小腺泡增生患者中,黑人男性在重复活检时癌症检出率显著更高。
既往高级别上皮内瘤变、非典型小腺泡增生、直肠指检和前列腺特异性抗原斜率是重复活检中前列腺癌的独立预测指标。在调整疾病特征后,种族因素接近但未达到显著意义。