Evidence map›Paper›PMID 40014208›Full record

ArticleAnnals of surgical oncology2025

Genetic Ancestry and 21-Gene Oncotype DX Breast Cancer Recurrence Scores.

Peter A Borowsky, Alexandra E Hernandez, Susan B Kesmodel, Neha Goel

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Article in Annals of surgical oncology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

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1citing papers in PubMed
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1 · What the graph read from it

What it found

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3 · Its place in the literature

Who cites it

1 citing paper in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

4 authors.

Peter A BorowskyDivision of Surgical Oncology, Dewitt Daughtry Department of Surgery, University of Miami, Miami, FL, USA.
Alexandra E HernandezDivision of Surgical Oncology, Dewitt Daughtry Department of Surgery, University of Miami, Miami, FL, USA.
Susan B KesmodelDivision of Surgical Oncology, Dewitt Daughtry Department of Surgery, University of Miami, Miami, FL, USA.
Neha GoelDivision of Surgical Oncology, Dewitt Daughtry Department of Surgery, University of Miami, Miami, FL, USA. goeln1@mskcc.org.

Funding

UM Calabresi Clinical Oncology Research Career Development AwardK12CA226330 · NCI · UNIVERSITY OF MIAMI SCHOOL OF MEDICINE · PI Alan Pollack · 2018 to 2026
$5.1M
NCI NIH HHS K12 CA226330
6 · The paper itself

Abstract

backgroundRacial and ethnic breast cancer disparities persist. This may be reflected by differences in Oncotype DX recurrence scores (RS), which are higher for Black women. This study assesses the association between ancestry and RS.

methodsStage I-III hormone receptor (HR)-positive, human epidermal growth factor receptor 2 (HER2)-negative breast cancer patients with ancestry and RS data were prospectively identified from 2017 to 2021. RS were grouped into low, intermediate, and high categories. Multinomial regression determined the association between ancestry and RS controlling for ancestry and estrogen receptor (ER), progesterone receptor (PR), and HER2 expression.

resultsOf 174 patients, 28 (16.1%) self-identified as non-Hispanic White, 107 (61.5%) self-identified as Hispanic White, 19 (10.9%) self-identified as non-Hispanic Black, and 9 (5.2%) self-identified as Hispanic Black. Ninety-four (54.0%) patients had low RS, 51 (29.3%) had intermediate RS, and 29 (16.7%) had high RS. On multivariable analyses, West African ancestry was associated with increased odds of intermediate (odds ratio [OR] 1.02, 95% confidence interval [CI] 1.00-1.04, p = 0.039) and high (OR 1.03, 95% CI 1.00-1.06, p = 0.022) RS. East Asian ancestry was associated with decreased odds of intermediate RS (OR 0.78, 95% CI 0.60-1.00, p = 0.048). Increasing ER (OR 0.43, 95% CI 0.23-0.82, p = 0.011), PR (OR 0.20, 95% CI 0.11-0.34, p < 0.001), and HER2 (OR 0.24, 95% CI 0.09-0.63, p = 0.004) expression were associated with lower odds of high RS.

conclusionIncreasing West African ancestry is associated with increased odds of high and intermediate RS, while increasing East Asian ancestry is associated with lower odds of intermediate RS. These findings require validation but suggest ancestry may represent a biological biomarker and that assays guiding adjuvant therapy may require ancestry-based calibration in HR+/HER2- tumors.

Indexed as

Biomarkers, TumorBreast NeoplasmsNeoplasm Recurrence, LocalAdultAgedBlack or African AmericanErb-b2 Receptor Tyrosine KinasesFemaleFollow-Up StudiesGene Expression ProfilingHispanic or LatinoHumansMiddle AgedPrognosisProspective StudiesReceptors, EstrogenBiomarkers, TumorERBB2 protein, humanErb-b2 Receptor Tyrosine KinasesReceptors, EstrogenReceptors, Progesterone

Identifiers

PMID40014208

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