Authors
Mehmet Zafer Sabuncuoglu, Ismail Zihni
Published in
Journal of racial and ethnic health disparities. Oct 28, 2026. Epub Oct 28, 2026.
Abstract
Racial/ethnic disparities in colorectal cancer mortality persist in the United States despite treatment advances. We examined racial/ethnic differences in guideline-concordant care (GCC) receipt and cancer-specific mortality, estimated the proportion of the Black-White disparity mediated through GCC, and tested for heterogeneity in the GCC-survival association across groups.
Population-based cohort study using the Surveillance, Epidemiology, and End Results (SEER) Program. Adults with a first primary colorectal adenocarcinoma diagnosed 2010-2017 were included (N = 45,267). GCC was operationalized as a composite score (0-4) per NCCN recommendations. The primary outcome, cancer-specific mortality (CSM), was analyzed using Fine-Gray subdistribution hazard models. Race/ethnicity x GCC interactions were tested by likelihood ratio test; causal mediation decomposed effects into mediated and direct components.
Among 45,267 patients (52% male), CSM occurred in 10,478 (23%) over a median 77 months. GCC receipt differed significantly across groups (all p < 0.001). Non-Hispanic Black patients had higher adjusted CSM than White patients (SHR 1.20, 95% CI 1.11-1.28); Asian/PI patients had lower CSM (SHR 0.86, 95% CI 0.78-0.95). A significant race x GCC interaction was identified (p = 0.0036), with a stronger GCC-CSM association among Black than White patients (interaction HR 0.907, 95% CI 0.847-0.971). GCC differences accounted for only 2.2% (95% CI 0.8-4.5%) of the Black-White disparity.
Racial/ethnic disparities in colorectal cancer mortality were not substantially explained by differences in GCC receipt. A significant race/ethnicity x GCC interaction indicated that Black patients derived greater survival benefit per care component. Equitable care delivery is important but insufficient to eliminate persistent disparities; structural and social determinants must also be addressed.
PMID:
42955181
Bibliographic data and abstract were imported from PubMed on 30 Oct 2026.
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