Analysis reveals low educational attainment correlates with worse mortality outcomes in older men with prostate cancer, suggesting community-level education impacts survivorship.
327 Background: Educational attainment shapes access, treatment, and survivorship in prostate cancer (PC), yet community-level effects remain underexplored. We tested whether residence in low-education counties is associated with prostate cancer-specific mortality (PCSM) and related outcomes in older men with PC. Methods: We analyzed SEER-Medicare (2009-2017) including men aged ≥66 years with incident PC. Low education was defined as counties where >15% of adults lack a high-school diploma. Outcomes were PCSM (primary), cardiovascular events (CVE), cardiovascular mortality (CVm), and all-cause mortality (ACM). Fine-Gray competing-risk and Cox models adjusted for demographics, comorbidities, stage/grade, and treatments. Prespecified subgroup analyses were conducted in non-Hispanic Black (NHB) and urban residents. Results: Median follow-up ranged 3.3-4.5 years among 109,724 complete cases of men (85,516 in high-education and 32,210 in low-education counties). Residence in low-education counties was associated with a higher but not statistically significant risk of PCSM (subdistribution hazard ratio [sHR] 1.06; 95% CI 0.95-1.19; p=0.29). In contrast, low-education residence was associated with higher risks of CVE (sHR 1.04; 95% CI 1.01-1.06; p=0.002), CVm (sHR 1.18; 95% CI 1.12-1.25; p<0.001), and ACM (adjusted HR 1.08; 95% CI 1.05-1.11; p<0.001). Similar trends were observed in NHB and urban populations. Conclusions: Living in counties with lower educational attainment was independently associated with higher cardiovascular and overall mortality after PC diagnosis, with a consistent directional trend toward increased PCSM. Community-level education is a structural determinant of survivorship and a practical target for geospatial outreach to improve outcomes. Association of county level educational attainment with mortality and cardiovascular outcomes across overall, NHB, and urban subgroups. Outcome (Model) Overall (aHR/sHR [95% CI], p) NHB (aHR/sHR [95% CI], p) Urban (aHR/sHR [95% CI], p) PCSM (Fine-Gray) 1.06 (0.95–1.19, p=0.29) 1.08 (0.95–1.23, p=0.25) 1.12 (0.90–1.41, p=0.32) CVE (Fine-Gray) 1.04 (1.01–1.06, p=0.002) 0.98 (0.92–1.05, p=0.53) 1.02 (1.00–1.04, p=0.10) CVm (Fine-Gray) 1.18 (1.12–1.25, p<0.001) 1.08 (0.92–1.27, p=0.36) 1.17 (1.10–1.25, p<0.001) ACM (Cox) 1.08 (1.05–1.11, p<0.001) 1.11 (1.02–1.20, p=0.02) 1.05 (1.02–1.09, p<0.001) Sample sizes: Overall N = 109,724; NHB N = 11,726; Urban N = 93,318. Fine-Gray models account for competing risk of death, and Cox proportional hazards models were used for all-cause mortality. Models adjusted for age, race, marital status, socioeconomic status, rurality, prostate cancer stage and grade, diabetes, hypertension, hyperlipidemia, chronic kidney disease, surgery, radiation, chemotherapy, and prior cardiovascular events.
No takes yet. Share an insight, caveat, or question.
Shah et al. (2026) studied this question.
Synapse has enriched 5 closely related papers on similar clinical questions. Consider them for comparative context: