Evidence map›Paper›PMID 32986828›Full record

Trial reportJournal of the National Cancer Institute2021

Race, Ethnicity, and Clinical Outcomes in Hormone Receptor-Positive, HER2-Negative, Node-Negative Breast Cancer in the Randomized TAILORx Trial.

Kathy S Albain, Robert J Gray, Della F Makower, Amir Faghih, Daniel F Hayes, Charles E Geyer, Elizabeth C Dees, Matthew P Goetz, John A Olson, Tracy Lively and 18 more

Open access · greenAbstract readRandomized Controlled Trial
In one paragraph

Trial report in Journal of the National Cancer Institute, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 73 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
73citing papers in PubMed, 1 pooled it
5.2field-weighted citation impact, top 3% of its field
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

73 citing papers in PubMed, 1 synthesis or guideline pooled it, 110 citations in OpenAlex.

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13 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

28 authors at 20 institutions in 4 countries.

Kathy S AlbainLoyola University Chicago Stritch School of Medicine, Cardinal Bernadin Cancer Center, Loyola University Medical Center, Maywood, IL, USA.
Robert J GrayDana Farber Cancer Institute, Boston, MA, USA.
Della F MakowerMontefiore Medical Center, Albert Einstein College of Medicine, Bronx, NY, USA.
Amir FaghihThunder Bay Regional Health Science Centre, Thunder Bay, Ontario, Canada.
Daniel F HayesUniversity of Michigan, Ann Arbor, MI, USA.
Charles E GeyerHouston Methodist Cancer Center, Houston, TX, USA.
Elizabeth C DeesUniversity of North Carolina, Chapel Hill, NC, USA.
Matthew P GoetzMayo Clinic, Rochester, MN, USA.
John A OlsonUniversity of Maryland School of Medicine, Baltimore, MD, USA.
Tracy LivelyNational Institutes of Health, National Cancer Institute, Bethesda, MD, USA.
Sunil S BadveIndiana University School of Medicine, Indianapolis, IN, USA.
Thomas J SaphnerAurora Health Care, Two Rivers, WI, USA.
Lynne I WagnerWake Forest University Health Service, Winston Salem, NC, USA.
Timothy J WhelanMcMaster University, Hamilton, Canada.
Matthew J EllisBaylor College of Medicine, Houston, TX, USA.
William C WoodEmory University, Atlanta, GA, USA.
Maccon M KeaneCancer Trials Ireland, Dublin, Ireland.
Henry L GomezInstituto Nacional de Enfermedades Neoplasicas, Lima, Peru.
Pavan S ReddyCancer Center of Kansas, Wichita, KS, USA.
Timothy F GogginsFox Valley Hematology and Oncology, Appleton, WI, USA.
Ingrid A MayerVanderbilt University, Nashville, TN, USA.
Adam M BrufskyUniversity of Pittsburgh, Pittsburgh, PA, USA.
Deborah L ToppmeyerRutgers Cancer Institute of New Jersey, New Brunswick, NJ, USA.
Virginia G KaklamaniUniversity of Texas, San Antonio, TX, USA.
Jeffrey L BerenbergUniversity of Hawaii Cancer Center, Honolulu, HI, USA.
Jeffrey AbramsNational Institutes of Health, National Cancer Institute, Bethesda, MD, USA.
George W SledgeStanford University, Stanford, CA, USA.
Joseph A SparanoMontefiore Medical Center, Albert Einstein College of Medicine, Bronx, NY, USA.
Albert Einstein College of Medicine · USNational Institutes of Health · USAurora Health Care · USBaylor College of Medicine · USCancer Center of Kansas · USCancer Trials Ireland · IEDana-Farber Cancer Institute · USEmory University · USFox Valley Technical College · USHouston Methodist · USIndiana University School of MedicineInstituto Nacional de Enfermedades Neoplásicas · PELoyola University Medical Center · USMayo Clinic in Arizona · USMcMaster University · CARutgers, The State University of New Jersey · USStanford University · USThe University of Texas at San Antonio · USThunder Bay Regional Health Sciences Centre · CAUniversity of Hawaiʻi at Mānoa · US

Funding

NRG Oncology Network Group Operations Center - GY9 BIQSFP Reports/BudgetsU10CA180868 · NCI · NRG ONCOLOGY FOUNDATION, INC. · PI NORMAN WOLMARK · 2014 to 2026
$206.8M
ECOG-ACRIN NCORP Research Base - TMISTUG1CA189828 · NCI · ECOG-ACRIN MEDICAL RESEARCH FOUNDATION · PI Peter J ODwyer, MITCHELL D. SCHNALL · 2014 to 2026
$199.7M
Member Site CoreU10CA180821 · NCI · BRIGHAM AND WOMEN'S HOSPITAL · PI Evanthia Galanis · 2014 to 2026
$177.3M
Project-006U10CA180820 · NCI · ECOG-ACRIN MEDICAL RESEARCH FOUNDATION · PI Peter J ODwyer · 2014 to 2026
$167.6M
SWOG Network Group Operations Center of the NCTNU10CA180888 · NCI · UNIVERSITY OF CALIFORNIA AT DAVIS · PI PRIMO N. LARA · 2014 to 2026
$152.1M
Statistics CoreU10CA180822 · NCI · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI James J. Dignam, GREG YOTHERS · 2014 to 2026
$146.4M
NRG Oncology NCORP Research Base-BIQSFPUG1CA189867 · NCI · NRG ONCOLOGY FOUNDATION, INC. · PI Deborah Watkins Bruner, Lisa A. Kachnic · 2014 to 2026
$140.5M
Statistics CoreU10CA180794 · NCI · DANA-FARBER CANCER INST · PI PAUL J CATALANO, CONSTANTINE A. GATSONIS · 2014 to 2026
$111.2M
SWOG NCORP Research BaseUG1CA189974 · NCI · THE HOPE FOUNDATION · PI CHARLES D. BLANKE, DAWN HERSHMAN · 2014 to 2026
$80.6M
TISSUE CoreP50CA098131 · NCI · VANDERBILT UNIVERSITY MEDICAL CENTER · PI PARK, BEN HO, PIETENPOL, JENNIFER A · 2003 to 2024
$48.7M
ECOG-ACRIN Biospecimen Bank to Support NCTNU24CA196172 · NCI · ECOG-ACRIN MEDICAL RESEARCH FOUNDATION · PI STANLEY R. HAMILTON, Scott D Jewell · 2015 to 2026
$41.1M
NCIC Clinical Trials Group - Canadian Collaborating Clinical Trials NetworkU10CA180863 · NCI · QUEEN'S UNIVERSITY AT KINGSTON · PI Janet Ellen Dancey · 2014 to 2026
$40.4M
NCI NIH HHS P50 CA098131NCI NIH HHS U10 CA180794NCI NIH HHS U10 CA180820NCI NIH HHS U10 CA180821NCI NIH HHS U10 CA180822NCI NIH HHS U10 CA180863NCI NIH HHS U10 CA180868NCI NIH HHS U10 CA180888NCI NIH HHS U24 CA196172NCI NIH HHS UG1 CA189804NCI NIH HHS UG1 CA189828NCI NIH HHS UG1 CA189859NCI NIH HHS UG1 CA189867NCI NIH HHS UG1 CA189869NCI NIH HHS UG1 CA189974NCI NIH HHS UG1 CA190140NCI NIH HHS UG1 CA232760NCI NIH HHS UG1 CA233160NCI NIH HHS UG1 CA233184NCI NIH HHS UG1 CA233247NCI NIH HHS UG1 CA233253NCI NIH HHS UG1 CA233270NCI NIH HHS UG1 CA233373
6 · The paper itself

Abstract

backgroundBlack race is associated with worse outcomes in early breast cancer. We evaluated clinicopathologic characteristics, the 21-gene recurrence score (RS), treatment delivered, and clinical outcomes by race and ethnicity among women who participated in the Trial Assigning Individualized Options for Treatment.

methodsThe association between clinical outcomes and race (White, Black, Asian, other or unknown) and ethnicity (Hispanic vs non-Hispanic) was examined using proportional hazards models. All P values are 2-sided.

resultsOf 9719 eligible women with hormone receptor-positive, HER2-negative, node-negative breast cancer, there were 8189 (84.3%) Whites, 693 (7.1%) Blacks, 405 (4.2%) Asians, and 432 (4.4%) with other or unknown race. Regarding ethnicity, 889 (9.1%) were Hispanic. There were no substantial differences in RS or ESR1, PGR, or HER2 RNA expression by race or ethnicity. After adjustment for other covariates, compared with White race, Black race was associated with higher distant recurrence rates (hazard ratio [HR] = 1.60, 95% confidence intervals [CI] = 1.07 to 2.41) and worse overall survival in the RS 11-25 cohort (HR = 1.51, 95% CI = 1.06 to 2.15) and entire population (HR = 1.41, 95% CI = 1.05 to 1.90). Hispanic ethnicity and Asian race were associated with better outcomes. There was no evidence of chemotherapy benefit for any racial or ethnic group in those with a RS of 11-25.

conclusionsBlack women had worse clinical outcomes despite similar 21-gene assay RS results and comparable systemic therapy in the Trial Assigning Individualized Options for Treatment. Similar to Whites, Black women did not benefit from adjuvant chemotherapy if the 21-gene RS was 11-25. Further research is required to elucidate the basis for this racial disparity in prognosis.

Indexed as

AdultAgedAsian PeopleBlack PeopleBreast NeoplasmsComorbidityConfidence IntervalsErb-b2 Receptor Tyrosine KinasesEstrogen Receptor alphaFemaleHispanic or LatinoHumansInsurance CoverageIntracellular Signaling Peptides and ProteinsMenopauseMiddle AgedERBB2 protein, humanErb-b2 Receptor Tyrosine KinasesESR1 protein, humanEstrogen Receptor alphaIntracellular Signaling Peptides and ProteinsMRFAP1 protein, humanNuclear Proteins

Identifiers

PMID32986828
PMCPMC8599918
OpenAlexW3089593691

What OpenQuestion holds

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Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.