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Social, Structural, and Lifestyle Drivers of Prostate Cancer Disparities

Social, Structural, and Lifestyle Drivers of Prostate Cancer Disparities

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT07690579
Enrollment
350
Registered
2026-07-08
Start date
2026-03-31
Completion date
2028-03-31
Last updated
2026-07-08

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Prostate Cancer, Prostate Cancer Recurrent, Prostate Metastases

Keywords

Radical Prostatectomy

Brief summary

Prostate Cancer (PC) is the most common non-cutaneous malignancy diagnosed and second leading cause of cancer death among men across the United States. PC among Black men accounts for a higher proportion alike of cancer diagnoses and deaths. In the prostate specific antigen (PSA)-based screening era, mortality rates improved at a similar velocity among Black and White men, but the 2- to 3-fold excess mortality burden borne by Black men has persisted over the past 40 years, the second highest among all major cancers. In recent years mortality is rising among Black men, and at a rapid velocity. The explanations for this disparity-the extent to which it is attributable to genetics, environmental factors including Structural and Social Determinants of Health (SSDH), or access to care-are multifactorial and have been elucidated to a limited extent. A large meta-analysis recently found that across dozens of studies and cohorts, greater adjustment for clinical and SSDH factors generally resulted in race itself dropping as a significant predictor. These and other findings suggest that the determinants of disparity be identified at time of, and prior to, cancer diagnosis, and that both genetic and environmental factors contribute to earlier development and progression.

Detailed description

The investigators hypothesize that SSDH factors drive cancer development differentially by race, and including SSDH factors in prediction models can improve risk prediction to guide decision-making regarding screening, diagnosis, and treatment across race and ethnic groups. PRIMARY OBJECTIVE: To identify not yet discovered SSDH and lifestyle factors that associate with identification of unfavorable vs. favorable prostate cancer histology between Black, Hispanic, and Asian men. OUTLINE: UCSF participants who agreed to participate in the Urology 90991 Biobank Consent (UCSF internal review board (IRB) #11-05226), and urology surgeons at community hospitals may refer participants for radical prostatectomy to University of California, San Francisco. Potential participants will be approached by the UCSF study team for an offer to participate and Non-UCSF participants will be asked to sign a medical release form prior to the research team collecting data from your medical record about your prostate cancer and treatment.

Interventions

OTHERQuestionnaires

Participants will receive surveys to complete online via a secure system.

Data will be collected from participants medical charts which includes disease history, pathological findings, and other disease characteristics.

Sponsors

University of California, San Francisco
Lead SponsorOTHER
National Cancer Institute (NCI)
CollaboratorNIH

Study design

Observational model
CASE_CONTROL
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
MALE
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Participants who have elected radical prostatectomy as prostate cancer treatment. * Participants who have agreed to participate in the Urology Biobank.

Exclusion criteria

* Participant does not plan nor schedule a radical prostatectomy (RP) procedure.

Design outcomes

Primary

MeasureTime frameDescription
Identification of not yet identified factors contributing to prostate cancerUp to 2 yearsGenomic and SSDH factors will be evaluated to locate not yet identified factors that are associated with greater immune activation and prediction of unfavorable vs. favorable prostate cancer biology by race and ethnicity groups.

Countries

United States

Contacts

CONTACTKiana Washington
Kiana.Washington@ucsf.edu415.514.8026
CONTACTKarina Acevedo
Karina.Acevedo@ucsf.edu415.353.7615
PRINCIPAL_INVESTIGATORMatthew Cooperberg, MD

University of California, San Francisco

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Jul 9, 2026