Racial Disparities in Future Development of Lethal Prostate Cancer Based on Midlife Baseline Prostate-Specific Antigen.

IF 2.6 3区 医学 Q3 ENDOCRINOLOGY & METABOLISM Prostate Pub Date : 2025-03-01 Epub Date: 2024-12-09 DOI:10.1002/pros.24834
Giuseppe Chiarelli, Matthew Davis, Alex Stephens, Marco Finati, Giuseppe Ottone Cirulli, Chase Morrison, Akshay Sood, Giuseppe Carrieri, Alberto Briganti, Francesco Montorsi, Giovanni Lughezzani, Nicolò Buffi, Craig Rogers, Firas Abdollah
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Abstract

Background: Previous studies found that Midlife Baseline PSA (MB PSA) predicts the risk of developing lethal prostate cancer (PCa), although the cohorts were homogenous in terms of racial compositions. We aimed to investigate racial disparities in the predictive value of MB PSA for lethal PCa in a diverse, contemporary, North American population.

Methods: Our cohort included White and Black men aged 40-59 years, who underwent MB PSA through our health system. Cumulative incidence curves depicted lethal PCa stratified by race and MB PSA above/below the median. We utilized time-dependent Receiver Operating Characteristic (ROC) curves and Area Under the ROC Curve (AUC) to compare the performance of MB PSA in predicting lethal PCa based on race. Multivariable regression (MVA) was used to examine the impact of the MB PSA in predicting lethal PCa by race.

Results: We included 112,967 men, of whom 27% were Black. The cumulative incidence estimate with MB PSA values equal to the median at 15 years of follow-up was 0.13 (0.04, 0.32) for White men and 0.55 (0.24, 1.11) for Black men. AUCs comparison showed no statistically significant differences in the predictive role of MB PSA for lethal PCa between White and Black men. At MVA, using White patients with PSA ≤ median as the reference group, the HR of lethal PCa for White men with PSA > median aged 40-44, 45-49, 50-54, and 55-59 was respectively 2.98 (1.59-5.57), 3.01 (1.89-4.81), 5.10 (3.38-7.70), and 3.38 (2.32-4.92). While for Black men was respectively 5.50 (2.94-10.27), 4.19 (2.59-6.78), 9.79 (6.37-15.04), and 7.53 (5.03-11.26) (all p < 0.001).

Conclusion: Our findings indicate that for the same MB PSA and within the same age category, Black men have a greater risk of developing lethal PCa than White men. A separate cut-off should be created for MB PSA, if this is to be used to guide PSA screening in clinical practice.

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基于中年基线前列腺特异性抗原的致死性前列腺癌未来发展的种族差异。
背景:先前的研究发现,中年基线PSA (MB PSA)预测发生致死性前列腺癌(PCa)的风险,尽管队列在种族组成方面是同质的。我们的目的是在不同的当代北美人群中调查MB PSA对致死性PCa的预测价值的种族差异。方法:我们的队列包括40-59岁的白人和黑人男性,他们通过我们的卫生系统接受了MB PSA。累积发病率曲线描绘了按种族和MB PSA高于/低于中位数分层的致死性PCa。我们利用随时间变化的受试者工作特征(ROC)曲线和ROC曲线下面积(AUC)来比较MB PSA预测基于种族的致死性PCa的性能。采用多变量回归(MVA)来检验MB PSA在预测种族致死性PCa中的影响。结果:我们纳入了112,967名男性,其中27%为黑人。在15年随访时,MB PSA值等于中位值的累积发病率估计为白人男性0.13(0.04,0.32),黑人男性0.55(0.24,1.11)。auc比较显示,MB PSA对白人和黑人男性致死性前列腺癌的预测作用无统计学差异。在MVA,以PSA≤中位数的白人患者为参照组,40-44岁、45-49岁、50-54岁和55-59岁中位数PSA为>的白人男性致死性前列腺癌的HR分别为2.98(1.59-5.57)、3.01(1.89-4.81)、5.10(3.38-7.70)和3.38(2.32-4.92)。而黑人男性分别为5.50(2.94 ~ 10.27)、4.19(2.59 ~ 6.78)、9.79(6.37 ~ 15.04)和7.53(5.03 ~ 11.26)(均为p)。结论:在同一年龄段,相同MB PSA,黑人男性发生致死性PCa的风险高于白人男性。如果要在临床实践中用于指导PSA筛查,则应为MB PSA创建单独的截止值。
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来源期刊
Prostate
Prostate 医学-泌尿学与肾脏学
CiteScore
5.10
自引率
3.60%
发文量
180
审稿时长
1.5 months
期刊介绍: The Prostate is a peer-reviewed journal dedicated to original studies of this organ and the male accessory glands. It serves as an international medium for these studies, presenting comprehensive coverage of clinical, anatomic, embryologic, physiologic, endocrinologic, and biochemical studies.
期刊最新文献
Evaluating the Prognostic Impact of Apparent Diffusion Coefficient in Definitive Radiotherapy for Gleason Score 7 Prostate Cancer Patients. Comparison of Prognosis and Health-Related Quality of Life Between Robot-Assisted Radical Prostatectomy Versus High-Dose-Rate Brachytherapy Combined With External Beam Radiation Therapy and Hormone Therapy for High-Risk Prostate Cancer. ERG and PTEN Role on Active Surveillance for Low-Risk Prostate Cancer in the Multiparametric MRI Era. Racial Disparities in Future Development of Lethal Prostate Cancer Based on Midlife Baseline Prostate-Specific Antigen. Histopathologic Features and Transcriptomic Signatures Do Not Solve the Issue of Magnetic Resonance Imaging-Invisible Prostate Cancers: A Matched-Pair Analysis.
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