Evidence map›Paper›PMID 42350394›Full record

ArticleNPJ breast cancer2026

Prognostic consistency of oncotype DX® molecular assay across racial groups in early-stage hormone receptor-positive breast cancer.

Reine Abou Zeidane, Benjamin Hauk, Samuel Lichtman-Mikol, Courtney Pisano, Yilun Sun, Priyanka Shailendra Rana, Citlally Lopez-Flores, Breanna N McBean, Kassidy M Jungles, Trisha Lal and 6 more

Abstract read
In one paragraph

Article in NPJ breast cancer, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0cells of the map it votes in
0citing papers in PubMed
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1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

16 authors.

Reine Abou ZeidaneCase Western Reserve University School of Medicine, Cleveland, OH, USA.
Benjamin HaukCase Western Reserve University School of Medicine, Cleveland, OH, USA.
Samuel Lichtman-MikolCase Western Reserve University School of Medicine, Cleveland, OH, USA.
Courtney PisanoCase Western Reserve University School of Medicine, Cleveland, OH, USA.
Yilun SunCase Western Reserve University School of Medicine, Cleveland, OH, USA.
Priyanka Shailendra RanaCase Western Reserve University School of Medicine, Cleveland, OH, USA.
Citlally Lopez-FloresUniversity of Nevada School of Medicine, Las Vegas, NV, USA.
Breanna N McBeanUniversity of Michigan School of Medicine, Ann Arbor, MI, USA.
Kassidy M JunglesUniversity of Michigan School of Medicine, Ann Arbor, MI, USA.
Trisha LalCase Western Reserve University School of Medicine, Cleveland, OH, USA.
Nihit MehtaCase Western Reserve University School of Medicine, Cleveland, OH, USA.
Philip BomeislCase Western Reserve University School of Medicine, Cleveland, OH, USA.
Amanda L AminCase Western Reserve University School of Medicine, Cleveland, OH, USA.
Alberto J MonteroCase Western Reserve University School of Medicine, Cleveland, OH, USA.
Janice LyonsCase Western Reserve University School of Medicine, Cleveland, OH, USA.
Corey W SpeersCase Western Reserve University School of Medicine, Cleveland, OH, USA. Cspeers@uabmc.edu.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

In this retrospective cohort study, we evaluated the consistency of prognostic outcomes provided by the Oncotype DX® assay across different racial groups among women with early-stage hormone receptor-positive (HR + ) breast cancer. Data was abstracted from the electronic medical record of 1122 patients with non-metastatic HR+ breast cancer who underwent Oncotype DX testing at University Hospitals Seidman Cancer Center between 2013 and 2023. Recurrence Score (RS) categories were defined using historical cutpoints: low(0-18), intermediate(19-30), and high(31-100). Two contemporary-cutpoint sensitivity analyses based on TAILORx and RxPONDER were also performed: binary scheme (0-25;26-100) and three-level scheme (RS 0-15;16-25;26-100). Recurrence-free survival (RFS) and overall survival (OS) were analyzed using Kaplan-Meier curves and adjusted Cox models. The cohort included 142 African American (AA) and 967 White women. Under the historical cutpoints, AA women had a higher prevalence of intermediate and high-risk RS. Despite these differences, 5-year RFS and OS were comparable. In multivariable analyses, AA race was not independently associated with RFS or OS. Sensitivity analyses using contemporary cutpoints yielded concordant findings. These findings support consistent prognostic value of Oncotype DX assay across racial groups, although further investigation into socioeconomic and clinical contributors to disparities is warranted.

Identifiers

PMID42350394
PMCPMC13658793

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