# Modeling the Effect of Treatments on Prostate Cancer-Specific Mortality and the Relevant Geographical Variation and Racial Disparities

**Authors:** Wensheng Zhang, Christopher Williams, Guangdi Wang, Kun Zhang

PMC · DOI: 10.3390/cancers18060983 · Cancers · 2026-03-18

## TL;DR

Black prostate cancer patients in the U.S. face higher mortality risks, partly due to treatment disparities that vary by geography.

## Contribution

This study links treatment disparities to racial mortality gaps in prostate cancer using large-scale data analysis.

## Key findings

- Surgery alone significantly reduces mortality risk compared to radiotherapy or combined treatments.
- Including treatment in models reduces the estimated mortality risk for Black patients.
- Geographic treatment disparities correlate with racial differences in prostate cancer mortality.

## Abstract

Black American prostate cancer (PCa) patients have a higher risk of dying from the disease and are less likely to undergo radical treatment than White Americans. Mortality disparities vary geographically. This study investigated the impact of treatments on PCa-specific mortality and the relevant disparities. Using the Cox proportional hazards (Cox PH) model and other statistical methods, we analyzed two datasets extracted from the SEER and PLCO databases. The primary findings were as follows: the relative mortality risk (RR) of patients undergoing surgery alone was significantly lower than that of patients receiving radiotherapy alone or a combination of surgery and radiotherapy; Black patients’ RR estimated by the model including treatment was substantially smaller than that estimated by the reduced model excluding treatment; and across geographic areas, racial disparities in mortality were associated with disparities in treatment. These findings provide new insight into the etiology of the poorer survival of Black patients.

Background/Objectives: African American (Black) prostate cancer (PCa) patients have a higher risk of dying from the disease and are less likely to undergo radical treatment than European Americans (White). The disparities in PCa-specific mortality (PCSM) and mortality rate (PCSMR) vary geographically. This study investigated the impact of treatments on PCSM, PCSMR and the relevant disparities. Methods: Using the Cox PH model and other statistical methods, we analyzed two datasets extracted from the SEER and PLCO databases. The SEER dataset contains 637,093 White patients and 110,839 Black patients. The PLCO dataset included 7463 Whites and 495 Blacks, and supplemented the SEER data with information on PCa family history (pros_fh). Results: Analysis of SEER data showed that the relative mortality risk (RR) of patients undergoing surgery alone was significantly lower than that of patients receiving radiotherapy alone or a combination of surgery and radiotherapy. Black patients’ RR estimated by the model including treatment was substantially smaller than that estimated by the reduced model excluding treatment. The differences between Black and White in the three-nine-year PCSMR of patients with high-grade or non-localized cancer were significantly correlated with the differences in surgery alone rate (r < −0.65, p < 0.001). Regression-based mediation analysis indicated that treatment disparity had a significant direct effect on mortality disparity and did not mediate the effect of age disparity. Analysis of PLCO data showed that pros_fh had no significant effect on survival but confirmed the survival advantage of surgery over radiotherapy. Conclusions: The results of this study support the hypothesis that, for PCa patients in the United States, geographical variation in treatment disparity partially explains variation in mortality disparity.

## Linked entities

- **Diseases:** prostate cancer (MONDO:0005159)

## Full-text entities

- **Diseases:** cancer (MESH:D009369), PCa (MESH:D011471)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

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## Figures

6 figures with captions in the complete paper: https://tomesphere.com/paper/PMC13024551/full.md

## References

51 references — full list in the complete paper: https://tomesphere.com/paper/PMC13024551/full.md

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Source: https://tomesphere.com/paper/PMC13024551