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Prostate cancer care disparities: treatment gaps, access barriers, and the impact of screening recommendations on the Non-Hispanic Black community
Dissertation

Prostate cancer care disparities: treatment gaps, access barriers, and the impact of screening recommendations on the Non-Hispanic Black community

Gawain Javon Williams
University of Iowa
Doctor of Philosophy (PhD), University of Iowa
Spring 2026
DOI: 10.25820/etd.008456
pdf
Gawain Williams Dissertation FINAL1.57 MB
Embargoed Access, Embargo ends: 06/29/2028

Abstract

Prostate cancer (PCa) is one of the most frequently diagnosed cancers and a leading cause of cancer-related death among men in the United States. Non-Hispanic Black (NHB) men bear a disproportionate burden, experiencing higher incidence, earlier age at onset, and greater mortality compared to other racial and ethnic groups. While biological susceptibility has been previously identified, a growing body of work suggests that disparities in prostate cancer outcomes cannot be explained by genetics alone. Differences in screening access, timeliness of care, systemic barriers, healthcare experiences, and broader social determinants of health play critical roles in shaping outcomes for NHB men across the prostate cancer care continuum. This dissertation examined disparities in PCa screening, treatment, and access to care among NHB men through three complementary studies. The first study evaluated racial differences in definitive treatment and time to treatment initiation in Iowa using Iowa Cancer Registry data. NHB men with advanced stage PCa were less likely to receive definitive treatment compared to (Non-Hispanic White) NHW men and experienced longer delays to adjuvant therapy, despite a higher proportion receiving care at National Cancer Institute-designated or Commission on Cancer- accredited facilities. The second study explored barriers and access challenges experienced by NHB individuals seeking cancer care in Iowa, through key-informant interviews with Black community leaders and stakeholders. The analysis identified themes related to health literacy and cultural understanding, structural barriers to care, interpersonal dynamics and communication, trust within the healthcare system, strengths and resiliencies, as well as community-based solutions for improving access to cancer care across the continuum. Comparative findings highlighted both shared and distinct experiences between African American and Black African immigrants, particularly in relation to health literacy and trust in the healthcare system. The third study evaluated the impact of the 2018 United States Preventive Services Task Force recommendation on Prostate-Specific Antigen (PSA) screening and PSA screening related conversations. Using Behavioral Risk Factor Surveillance System (BRFSS) data from 2010-2020, we applied a weighted continuous difference-in-difference approach with state and year fixed effects to examine changes in screening and shared decision making across baseline screening contexts. The findings revealed reductions in screening in previously high-screening states alongside a shift toward more balanced shared decision making. Together, these studies demonstrated the impact of the differences in treatment patterns, care access, and communication contribute to persistent disparities in PCa outcomes, offering evidence to inform future clinical practice and policy aimed to strengthen shared decision-making guidelines, improve equitable access to timely and high-quality cancer care, and support targeted, community-informed interventions to reduce disparities in PCa outcomes.
Prostate Cancer Cancer Health Disparities Health Policy PSA Screening Racial Disparities

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