Loeb Stacy, Roehl Kimberly A, Antenor Jo Ann V, Catalona William J, Suarez Brian K, Nadler Robert B
Department of Urology, Northwestern University Feinberg School of Medicine, Chicago, Illinois 60611, USA.
Urology. 2006 Feb;67(2):316-20. doi: 10.1016/j.urology.2005.08.040. Epub 2006 Jan 25.
Limited data are available concerning the extent to which the initial prostate-specific antigen (PSA) measurement in men younger than age 60 predicts for the risk of prostate cancer (CaP) and how this compares to other known risk factors.
From 1991 to 2001, 13,943 men younger than 60 years old participated in a CaP screening study. Men aged 40 to 49 years were eligible for the study if they had a positive family history or African-American heritage, and men older than 50 years were screened without respect to risk factors. The CaP detection rate, PSA velocity, pathologic features, and treatment outcomes were evaluated as a function of the baseline PSA level.
The median PSA level was 0.7 ng/mL for men aged 40 to 49 years and 0.9 ng/mL for men aged 50 to 59. A baseline PSA level between the median and 2.5 ng/mL was associated with a 14.6-fold and 7.6-fold increased risk of CaP in men aged 40 to 49 and 50 to 59 years, respectively. A greater baseline PSA value was also associated with a significantly greater PSA velocity, more aggressive tumor features, a greater biochemical progression rate, and a trend toward a greater cancer-specific mortality rate.
In men younger than 60, a baseline PSA value between the age-specific median and 2.5 ng/mL was a significant predictor of later CaP and was associated with a significantly greater PSA velocity. A young man's baseline PSA value was a stronger predictor of CaP than family history, race, or suspicious digital rectal examination findings. A greater baseline PSA level was associated with significantly more adverse pathologic features and biochemical progression.
关于60岁以下男性初始前列腺特异性抗原(PSA)测量对前列腺癌(CaP)风险的预测程度以及与其他已知风险因素相比情况的数据有限。
1991年至2001年,13943名60岁以下男性参与了一项CaP筛查研究。40至49岁男性若有家族史阳性或非裔美国人血统则符合研究条件,50岁以上男性无论风险因素均进行筛查。将CaP检出率、PSA速度、病理特征和治疗结果作为基线PSA水平的函数进行评估。
40至49岁男性的PSA中位数水平为0.7 ng/mL,50至59岁男性为0.9 ng/mL。40至49岁和50至59岁男性中,基线PSA水平在中位数与2.5 ng/mL之间分别与CaP风险增加14.6倍和7.6倍相关。更高的基线PSA值还与显著更高的PSA速度、更具侵袭性的肿瘤特征、更高的生化进展率以及癌症特异性死亡率升高趋势相关。
在60岁以下男性中,特定年龄中位数与2.5 ng/mL之间的基线PSA值是后期CaP的重要预测指标,且与显著更高的PSA速度相关。年轻男性的基线PSA值比家族史、种族或可疑的直肠指检结果更能预测CaP。更高的基线PSA水平与明显更多的不良病理特征和生化进展相关。