Evidence map›Paper›PMID 33146377›Full record

ArticleJournal of the National Cancer Institute2021

Racial and Ethnic Differences in Multigene Hereditary Cancer Panel Test Results for Women With Breast Cancer.

Siddhartha Yadav, Holly LaDuca, Eric C Polley, Chunling Hu, Nancy Niguidula, Hermela Shimelis, Jenna Lilyquist, Jie Na, Kun Y Lee, Stephanie Gutierrez and 8 more

Open access · hybridAbstract read
In one paragraph

Article 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 27 papers.

0numbers the graph read from it
0cells of the map it votes in
27citing papers in PubMed
3.4field-weighted citation impact, top 7% 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

27 citing papers in PubMed, 36 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Review
  6. Article
  7. Article
  8. Translational breast cancer research : a journal focusing on translational research in breast cancer · 2025
    Review
  9. Article
  10. Article
  11. Review
  12. Article
  13. Review
  14. Article
  15. Article
  16. Article
  17. Article
  18. Article
  19. Contralateral Breast Cancer Risk Among Carriers of Germline Pathogenic Variants inJournal of clinical oncology : official journal of the American Society of Clinical Oncology · 2023
    Article
  20. Hereditary cancer syndromes.World journal of clinical oncology · 2023
    Review
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

18 authors at 5 institutions in 1 country.

Siddhartha YadavDepartment of Oncology, Mayo Clinic, Rochester, MN, USA.ORCID 0000-0003-4630-9903
Holly LaDucaAmbry Genetics Inc, Aliso Viejo, CA, USA.ORCID 0000-0002-3745-9072
Eric C PolleyDepartment of Health Sciences Research, Mayo Clinic, Rochester, MN, USA.
Chunling HuDepartment of Laboratory Medicine and Pathology, Mayo Clinic, Rochester, MN, USA.
Nancy NiguidulaAmbry Genetics Inc, Aliso Viejo, CA, USA.
Hermela ShimelisDepartment of Laboratory Medicine and Pathology, Mayo Clinic, Rochester, MN, USA.
Jenna LilyquistDepartment of Laboratory Medicine and Pathology, Mayo Clinic, Rochester, MN, USA.
Jie NaDepartment of Health Sciences Research, Mayo Clinic, Rochester, MN, USA.
Kun Y LeeDepartment of Laboratory Medicine and Pathology, Mayo Clinic, Rochester, MN, USA.
Stephanie GutierrezAmbry Genetics Inc, Aliso Viejo, CA, USA.
Amal YussufAmbry Genetics Inc, Aliso Viejo, CA, USA.
Steven N HartDepartment of Health Sciences Research, Mayo Clinic, Rochester, MN, USA.ORCID 0000-0001-7714-2734
Brigette Tippin DavisAmbry Genetics Inc, Aliso Viejo, CA, USA.
Elizabeth C ChaoAmbry Genetics Inc, Aliso Viejo, CA, USA.
Tina PesaranAmbry Genetics Inc, Aliso Viejo, CA, USA.ORCID 0000-0001-9807-4304
David E GoldgarHuntsman Cancer Institute, Department of Dermatology, University of Utah, Salt Lake City, UT, USA.
Jill S DolinskyAmbry Genetics Inc, Aliso Viejo, CA, USA.
Fergus J CouchDepartment of Laboratory Medicine and Pathology, Mayo Clinic, Rochester, MN, USA.ORCID 0000-0001-9417-9985
Ambry Genetics (United States) · USMayo Clinic in Arizona · USMayo Clinic in Florida · USUniversity of California, Irvine · USUniversity of Utah · US

Funding

Women's Cancer ProgramP30CA015083 · NCI · MAYO CLINIC ROCHESTER · PI Felicity Enders · 1985 to 2026
$151.3M
The Role of CHFR in Tumorigenesis and Paclitaxel-Sensitivity in Breast CancerP50CA116201 · NCI · MAYO CLINIC ROCHESTER · PI PETER C LUCAS · 2005 to 2026
$49.9M
Risk and penetrance of mutations from breast cancer testing panels.R01CA192393 · NCI · MAYO CLINIC ROCHESTER · PI COUCH, FERGUS JOSEPH, NATHANSON, KATHERINE L. · 2014 to 2018
$6.3M
Resolving the cancer relevance of predisposition gene mutationsR35CA253187 · NCI · MAYO CLINIC ROCHESTER · PI Fergus Joseph Couch · 2020 to 2026
$5.8M
Identifying and validating novel susceptibility genes for breast cancerR01CA176785 · NCI · MAYO CLINIC ROCHESTER · PI COUCH, FERGUS JOSEPH, NATHANSON, KATHERINE L. · 2014 to 2018
$3.4M
BRCA2 missense mutations and breast cancerR01CA116167 · NCI · MAYO CLINIC ROCHESTER · PI COUCH, FERGUS JOSEPH · 2007 to 2011
$3.0M
The contribution of RAD51C and RAD51D to breast and ovarian cancerR01CA225662 · NCI · MAYO CLINIC ROCHESTER · PI COUCH, FERGUS JOSEPH, WEROHA, SARAVUT · 2018 to 2024
$2.5M
NCI NIH HHS P30 CA015083NCI NIH HHS P50 CA116201NCI NIH HHS R01 CA116167NCI NIH HHS R01 CA176785NCI NIH HHS R01 CA192393NCI NIH HHS R01 CA225662NCI NIH HHS R35 CA253187
6 · The paper itself

Abstract

To evaluate the racial and ethnic differences in prevalence of germline pathogenic variants (PVs) and the effect of race and ethnicity on breast cancer (BC) risk among carriers, results of multigene testing of 77 900 women with BC (non-Hispanic White [NHW] = 57 003; Ashkenazi-Jewish = 4798; Black = 6722; Hispanic = 5194; and Asian = 4183) were analyzed, and the frequency of PVs in each gene were compared between BC patients (cases) and race- and ethnicity-matched gnomAD reference controls. Compared with NHWs, BRCA1 PVs were enriched in Ashkenazi-Jews and Hispanics, whereas CHEK2 PVs were statistically significantly lower in Blacks, Hispanics, and Asians (all 2-sided P < .05). In case-control studies, BARD1 PVs were associated with high risks (odds ratio > 4.00) of BC in Blacks, Hispanics, and Asians; ATM PVs were associated with increased risk of BC among all races and ethnicities except Asians, whereas CHEK2 and BRIP1 PVs were associated with increased risk of BC among NHWs and Hispanics only. These findings suggest a need for personalized management of BC risk in PV carriers based on race and ethnicity.

Indexed as

Breast NeoplasmsCase-Control StudiesEthnicityFemaleGenetic Predisposition to DiseaseHispanic or LatinoHumans

Identifiers

PMID33146377
PMCPMC8633452
OpenAlexW3095759315

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
Read underepoch 390

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.