Pan Charlie C, Lee Julia S, Chan June L, Sandler Howard M, Underwood Willie, McLaughlin Patrick W
Department of Radiation Oncology, University of Michigan, Ann Arbor, Michigan 48109, USA.
Int J Radiat Oncol Biol Phys. 2003 Dec 1;57(5):1292-6. doi: 10.1016/s0360-3016(03)00771-5.
We sought to determine whether African American men diagnosed with prostate cancer in the prostate-specific antigen (PSA) era differed in initial presenting serum PSA levels (iPSA) compared to white men. Recent retrospective studies have demonstrated higher iPSA within the African American men than in white men at the time of diagnosis, suggestive of more advanced disease in African American men. Both biologic differences and/or sociologic factors have been postulated as explaining the noted differences in iPSA. We reviewed our institution's PSA-era experience to determine any association between race and iPSA.
Between January 1990 and September 2001, 4519 patients representing a broad demographic sample were seen in the radiation oncology department of a university hospital or one of its four community affiliates. A total of 2332 eligible patients, with data on race, age, year of diagnosis, Gleason score, T stage, and iPSA, were analyzed. The patients were separated into the two following time periods for analysis, based on the new American Cancer Society screening guidelines: (1) 1991 to 1996 and (2) 1997 to 2001. The relationships between race and iPSA, T stage, Gleason score, and age are explored.
Of the 2332 patients analyzed, there were 1968 white men and 364 African American men. For the time period 1990 through 1996, the expected average (median) iPSA level was 10.5 (10.2) and 14.6 (15.8) for white men and African American men, respectively. For 1997 to 2001, the expected average iPSA level was 9.5 (8.4) and 10.8 (9.8), respectively. T stage distributions improved, independent of race, toward earlier stage at presentation. Gleason score distribution remained unchanged. African American men are 2.5-3.1 years younger than white men at diagnosis.
An overall decline in iPSA has occurred in both racial groups over time. More importantly, racial differences in iPSA among men diagnosed in the later time period (1997 to 2001) are less pronounced compared to men diagnosed in the earlier time period (1990 to 1996). This racial convergence in iPSA over time suggests improved penetrance of PSA screening in the African American population. Our findings also suggest that studies comparing racial differences in iPSA should consider time period of diagnosis and possible sociologic changes during that period (i.e., access to medical care, socioeconomic status, and educational level). The American Cancer Society guideline to begin screening African Americans at an earlier age is appropriate.
我们试图确定在前列腺特异性抗原(PSA)时代被诊断为前列腺癌的非裔美国男性与白人男性相比,其初始血清PSA水平(iPSA)是否存在差异。最近的回顾性研究表明,在诊断时非裔美国男性的iPSA高于白人男性,这表明非裔美国男性的疾病进展更为严重。生物学差异和/或社会因素被认为可以解释iPSA中存在的差异。我们回顾了我们机构在PSA时代的经验,以确定种族与iPSA之间的任何关联。
1990年1月至2001年9月期间,一所大学医院及其四个社区附属医院的放射肿瘤科共接待了4519名具有广泛人口统计学样本的患者。对总共2332名符合条件的患者进行了分析,这些患者有关于种族、年龄、诊断年份、Gleason评分、T分期和iPSA的数据。根据美国癌症协会新的筛查指南,将患者分为以下两个时间段进行分析:(1)1991年至1996年和(2)1997年至2001年。探讨了种族与iPSA、T分期、Gleason评分和年龄之间的关系。
在分析的2332名患者中,有1968名白人男性和364名非裔美国男性。在1990年至1996年期间,白人男性和非裔美国男性的预期平均(中位数)iPSA水平分别为10.5(10.2)和14.6(15.8)。在1997年至2001年期间,预期平均iPSA水平分别为9.5(8.4)和10.8(9.8)。T分期分布在就诊时独立于种族向更早阶段改善。Gleason评分分布保持不变。非裔美国男性在诊断时比白人男性年轻2.5 - 3.1岁。
随着时间的推移,两个种族群体的iPSA总体上都有所下降。更重要的是,与在早期时间段(1990年至1996年)被诊断的男性相比,在后期时间段(1997年至2001年)被诊断的男性中iPSA的种族差异不太明显。随着时间的推移,iPSA中的这种种族趋同表明PSA筛查在非裔美国人群中的普及率有所提高。我们的研究结果还表明,比较iPSA种族差异的研究应考虑诊断时间段以及该时间段内可能的社会变化(即获得医疗服务的机会、社会经济地位和教育水平)。美国癌症协会关于更早开始对非裔美国人进行筛查的指南是合适的。