Evaluating Prostate-Specific Antigen Screening for Young African American Men With Cancer

被引:6
|
作者
Qiao, Edmund M. [1 ,2 ]
Lynch, Julie A. [3 ]
Lee, Kyung M. [3 ]
Kotha, Nikhil, V [1 ,2 ]
Nalawade, Vinit [1 ,2 ]
Voora, Rohith S. [1 ,2 ]
Qian, Alexander S. [2 ]
Nelson, Tyler J. [1 ,2 ]
Yamoah, Kosj [4 ]
Garraway, Isla P. [5 ]
Stewart, Tyler F. [6 ]
Parsons, J. Kellogg [7 ]
Rose, Brent S. [1 ,2 ]
机构
[1] VA San Diego Hlth Care Syst, La Jolla, CA USA
[2] Univ Calif San Diego, Dept Radiat Med & Appl Sci, 3960 Hlth Sci Dr, San Diego, CA 92093 USA
[3] VA Salt Lake City Hlth Care Syst, Salt Lake City, UT USA
[4] H Lee Moffitt Canc Ctr & Res Inst, Dept Radiat Oncol, Tampa, FL USA
[5] Univ Calif Los Angeles, Dept Urol, Los Angeles, CA USA
[6] Univ Calif San Diego, Div Hematol Oncol, Dept Internal Med, La Jolla, CA 92093 USA
[7] Univ Calif San Diego, Dept Urol, San Diego, CA 92093 USA
来源
关键词
HEPATOCELLULAR-CARCINOMA; CLINICAL-TRIALS; PARTICIPATION; SURVEILLANCE; MORTALITY;
D O I
10.1093/jnci/djab221
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Background Despite higher risks associated with prostate cancer, young African American men are poorly represented in prostate-specific antigen (PSA) trials, which limits proper evidence-based guidance. We evaluated the impact of PSA screening, alongside primary care provider utilization, on prostate cancer outcomes for these patients. Methods We identified African American men aged 40-55 years, diagnosed with prostate cancer between 2004 and 2017 within the Veterans Health Administration. Inverse probability of treatment-weighted propensity scores were used in multivariable models to assess PSA screening on PSA levels higher than 20, Gleason score of 8 or higher, and metastatic disease at diagnosis. Lead-time adjusted Fine-Gray regression evaluated PSA screening on prostate cancer-specific mortality (PCSM), with noncancer death as competing events. All statistical tests were 2-sided. Results The cohort included 4726 patients. Mean age was 51.8 years, with 84-month median follow-up. There were 1057 (22.4%) with no PSA screening prior to diagnosis. Compared with no screening, PSA screening was associated with statistically significantly reduced odds of PSA levels higher than 20 (odds ratio [OR] = 0.56, 95% confidence interval [CI] = 0.49 to 0.63; P < .001), Gleason score of 8 or higher (OR = 0.78, 95% CI = 0.69 to 0.88; P < .001), and metastatic disease at diagnosis (OR = 0.50, 95% CI = 0.39 to 0.64; P < .001), and decreased PCSM (subdistribution hazard ratio = 0.52, 95% CI = 0.36 to 0.76; P < .001). Primary care provider visits displayed similar effects. Conclusions Among young African American men diagnosed with prostate cancer, PSA screening was associated with statistically significantly lower risk of PSA levels higher than 20, Gleason score of 8 or higher, and metastatic disease at diagnosis and statistically significantly reduced risk of PCSM. However, the retrospective design limits precise estimation of screening effects. Prospective studies are needed to validate these findings.
引用
收藏
页码:592 / 599
页数:8
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