Department of Urology, Osaka General Medical Center, Osaka, Japan.
J Urol. 2011 May;185(5):1722-7. doi: 10.1016/j.juro.2010.12.058. Epub 2011 Mar 21.
Asymptomatic prostatic inflammation may cause increased prostate specific antigen in some men, leading to unnecessary repeat prostate biopsy. We determined whether histological findings of inflammation in initial biopsy specimens and/or clinical indicators of inflammation could predict the outcome of subsequent biopsy in men with a negative initial biopsy.
A total of 105 Japanese men with increased prostate specific antigen underwent repeat prostate biopsy after initial biopsy revealed no evidence of carcinoma. Of the cases 45 (42.8%) were positive for prostate cancer at repeat biopsy. We evaluated initial biopsy specimens for evidence of inflammation by mononuclear and polymorphonuclear leukocytes, serum and urinary white blood count, and C-reactive protein.
Polymorphonuclear leukocyte infiltrates, urinary white blood count, patient age, prostate specific antigen at repeat biopsy, prostate volume, prostate specific antigen velocity and prostate specific antigen density were associated with the repeat biopsy outcome (p <0.05). Multivariate analysis revealed that age, prostate specific antigen density and urinary white blood count were independent predictors of outcome. On subgroup analysis of 63 men with serum prostate specific antigen less than 10 ng/ml before initial biopsy polymorphonuclear and mononuclear leukocyte inflammation, age, prostate specific antigen at repeat biopsy, prostate volume, prostate specific antigen velocity and prostate specific antigen density were associated with the outcome of repeat biopsy (p <0.05). Multivariate analysis showed that polymorphonuclear leukocyte infiltrate, prostate specific antigen density and age were independent predictors.
Age, prostate specific antigen density, polymorphonuclear leukocyte inflammation in initial biopsy specimens and urinary pyuria are indicators of benign repeat biopsy. They help avoid unnecessary repeat biopsy in men with increased prostate specific antigen.
前列腺炎症可能会导致一些男性的前列腺特异性抗原(PSA)水平升高,从而导致不必要的重复前列腺活检。本研究旨在确定初始活检标本中炎症的组织学发现和/或炎症的临床指标是否可以预测初次活检阴性男性的后续活检结果。
共有 105 名 PSA 升高的日本男性在初次活检未发现癌后接受了重复前列腺活检。其中 45 例(42.8%)在重复活检时被诊断为前列腺癌。我们通过单核细胞和多形核白细胞、血清和尿液白细胞计数以及 C 反应蛋白评估初始活检标本中的炎症证据。
多形核白细胞浸润、尿液白细胞计数、患者年龄、重复活检时的 PSA、前列腺体积、PSA 速度和 PSA 密度与重复活检结果相关(p<0.05)。多变量分析显示,年龄、PSA 密度和尿液白细胞计数是独立的预测因素。在初次活检前血清 PSA<10ng/ml 的 63 例男性亚组分析中,多形核和单核白细胞炎症、年龄、重复活检时的 PSA、前列腺体积、PSA 速度和 PSA 密度与重复活检结果相关(p<0.05)。多变量分析显示,多形核白细胞浸润、PSA 密度和年龄是独立的预测因素。
年龄、PSA 密度、初始活检标本中的多形核白细胞炎症和尿液脓尿是良性重复活检的指标。它们有助于避免 PSA 升高的男性进行不必要的重复活检。