3.8 Article

Outcomes of Hormone-Receptor Positive, HER2-Negative Breast Cancers by Race and Tumor Biological Features

Journal

JNCI CANCER SPECTRUM
Volume 5, Issue 1, Pages -

Publisher

OXFORD UNIV PRESS
DOI: 10.1093/jncics/pkaa072

Keywords

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Categories

Funding

  1. UNC Lineberger Comprehensive Cancer Center - University Cancer Research Fund [LCCC2017T204]
  2. Susan G. Komen Foundation
  3. National Cancer Institute of the National Institutes of Health [P50-CA58223, U01-CA179715, T32-CA057726, F30-CA236199]
  4. National Institute of Environmental Health Sciences of the National Institutes of Health [P30-ES010126]
  5. Gertrude B. Elion Mentored Medical Student Research Award of Triangle Community Foundation

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Black women with HR+/HER2-negative breast cancer have a higher risk of recurrence compared to White women, especially among those with aggressive tumors. Racial disparities in recurrence rates may be influenced by differences in treatment approaches. Identifying the causes of variations in cancer treatment is important for reducing outcome disparities.
Background: Black women have higher hormone receptor positive (HR+) breast cancer mortality than White women. Early recurrence rates differ by race, but little is known about genomic predictors of early recurrence among HR+ women. Methods: Using data from the Carolina Breast Cancer Study (phase III, 2008-2013), we estimated associations between race and recurrence among nonmetastatic HR+/HER2-negative tumors, overall and by PAM50 Risk of Recurrence score, PAM50 intrinsic subtype, and tumor grade using survival curves and Cox models standardized for age and stage. Relative frequency differences (RFD) were estimated using multivariable linear regression. To assess intervention opportunities, we evaluated treatment patterns by race among patients with high-risk disease. Results: Black women had higher recurrence risk relative to White women (crude hazard ratio = 1.81, 95% confidence interval [CI] = 1.34 to 2.46), which remained elevated after standardizing for clinical covariates (hazard ratio = 1.42, 95% CI = 1.05 to 1.93). Racial disparities were most pronounced among those with high PAM50 Risk of Recurrence score (5-year standardized recurrence risk = 18.9%, 95% CI = 8.6% to 29.1% in Black women vs 12.5%, 95% CI = 2.0% to 23.0% in White women) and high grade (5-year standardized recurrence risk = 16.6%, 95% CI = 11.7% to 21.5% in Black women vs 12.0%, 95% CI = 7.3% to 16.7% in White women). However, Black women with high-grade tumors were statistically significantly less likely to initiate endocrine therapy (RFD = -8.3%, 95% CI = -15.9% to -0.6%) and experienced treatment delay more often than White women (RFD = +9.0%, 95% CI = 0.3% to 17.8%). Conclusions: Differences in recurrence by race appear greatest among women with aggressive tumors and may be influenced by treatment differences. Efforts to identify causes of variation in cancer treatment are critical to reducing outcome disparities.

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