Evidence map›Paper›PMID 28724391›Full record

ArticleBreast cancer research : BCR2017

Hormone receptor status of a first primary breast cancer predicts contralateral breast cancer risk in the WECARE study population.

Anne S Reiner, Charles F Lynch, Julia S Sisti, Esther M John, Jennifer D Brooks, Leslie Bernstein, Julia A Knight, Li Hsu, Patrick Concannon, Lene Mellemkjær and 9 more

Open access · goldAbstract readMulticenter Study
In one paragraph

Article in Breast cancer research : BCR, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 21 papers.

0numbers the graph read from it
0cells of the map it votes in
21citing papers in PubMed
2.9field-weighted citation impact, top 9% 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

21 citing papers in PubMed, 41 citations in OpenAlex.

  1. Article
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  6. 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
  7. Tools for Contralateral Prophylactic Mastectomy Decision Making.Journal of clinical oncology : official journal of the American Society of Clinical Oncology · 2022
    Article
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  12. Review
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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

19 authors at 7 institutions in 4 countries.

Anne S ReinerMemorial Sloan Kettering Cancer Center, New York, NY, USA. reinera@mskcc.org.
Charles F LynchUniversity of Iowa, Iowa City, IA, USA.
Julia S SistiMemorial Sloan Kettering Cancer Center, New York, NY, USA.
Esther M JohnCancer Prevention Institute of California, Fremont, CA, USA.
Jennifer D BrooksUniversity of Toronto, Dalla Lana School of Public Health Sciences, Toronto, Canada.
Leslie BernsteinBeckman Research Institute, City of Hope National Medical Center, Duarte, CA, USA.
Julia A KnightUniversity of Toronto, Dalla Lana School of Public Health Sciences, Toronto, Canada.
Li HsuFred Hutchinson Cancer Research Center, Seattle, WA, USA.
Patrick ConcannonGenetics Institute and Department of Pathology, Immunology and Laboratory Medicine, University of Florida, Gainesville, FL, USA.
Lene MellemkjærDanish Cancer Society Research Center, Copenhagen, Denmark.
Marc TischkowitzDepartment of Medical Genetics, University of Cambridge, Cambridge, UK.
Robert W HaileStanford Department of Medicine, Division of Oncology, and the Stanford Cancer Institute, Stanford, CA, USA.
Ronglai ShenMemorial Sloan Kettering Cancer Center, New York, NY, USA.
Kathleen E MaloneFred Hutchinson Cancer Research Center, Seattle, WA, USA.
Meghan WoodsMemorial Sloan Kettering Cancer Center, New York, NY, USA.
Xiaolin LiangMemorial Sloan Kettering Cancer Center, New York, NY, USA.
Monica MorrowMemorial Sloan Kettering Cancer Center, New York, NY, USA.
Jonine L BernsteinMemorial Sloan Kettering Cancer Center, New York, NY, USA.
WECARE Study Collaborative Group
Memorial Sloan Kettering Cancer Center · USCancer Prevention Institute of California · USCity Of Hope National Medical Center · USUniversity of Cambridge · GBUniversity of Florida · USUniversity of Iowa · USUniversity of Toronto · CA

Funding

X-RAY CRYSTALLOGRAPHYP30CA008748 · NCI · SLOAN-KETTERING INSTITUTE FOR CANCER RES · PI Nicholas D Socci · 1985 to 2026
$347.4M
Viral VectorP30CA086862 · NCI · UNIVERSITY OF IOWA · PI Douglas Robert Spitz · 2000 to 2026
$70.0M
Genome-Wide Association Study of Radiation Exposure and Bilateral Breast CancerR01CA129639 · NCI · SLOAN-KETTERING INST CAN RESEARCH · PI BERNSTEIN, JONINE L. · 2009 to 2013
$15.6M
BREAST CANCER, RADIATION EXPOSURE, AND THE ATM GENEU01CA083178 · NCI · SLOAN-KETTERING INSTITUTE FOR CANCER RES · PI BERNSTEIN, JONINE LISA · 1999 to 2003
$9.3M
Molecular pathoepidemiology of contralateral breast cancerR01CA206464 · NCI · FRED HUTCHINSON CANCER RESEARCH CENTER · PI BERNSTEIN, JONINE L., MALONE, KATHLEEN E · 2017 to 2022
$7.0M
Interaction of Radiation, BRCA1/2, and Breast CancerR01CA097397 · NCI · SLOAN-KETTERING INSTITUTE FOR CANCER RES · PI BERNSTEIN, JONINE LISA · 2002 to 2006
$4.1M
Breast Cancer, Radiation and the ATM-CHEK2 PathwayR01CA114236 · NCI · SLOAN-KETTERING INSTITUTE FOR CANCER RES · PI BERNSTEIN, JONINE L. · 2005 to 2008
$1.8M
NCI NIH HHS P30 CA008748NCI NIH HHS R01 CA097397NCI NIH HHS R01 CA114236NCI NIH HHS R01 CA129639NCI NIH HHS R01 CA206464NCI NIH HHS U01 CA083178
6 · The paper itself

Abstract

backgroundPrevious population-based studies have described first primary breast cancer tumor characteristics and their association with contralateral breast cancer (CBC) risk. However, information on influential covariates such as treatment, family history of breast cancer, and BRCA1/2 mutation carrier status was not available. In a large, population-based, case-control study, we evaluated whether tumor characteristics of the first primary breast cancer are associated with risk of developing second primary asynchronous CBC, overall and in subgroups of interest, including among BRCA1/2 mutation non-carriers, women who are not treated with tamoxifen, and women without a breast cancer family history.

methodsThe Women's Environmental Cancer and Radiation Epidemiology Study is a population-based case-control study of 1521 CBC cases and 2212 individually-matched controls with unilateral breast cancer. Detailed information about breast cancer risk factors, treatment for and characteristics of first tumors, including estrogen receptor (ER) and progesterone receptor (PR) status, was obtained by telephone interview and medical record abstraction. Multivariable risk ratios (RRs) and 95% confidence intervals (CIs) were estimated in conditional logistic regression models, adjusting for demographics, treatment, and personal medical and family history. A subset of women was screened for BRCA1/2 mutations.

resultsLobular histology of the first tumor was associated with a 30% increase in CBC risk (95% CI 1.0-1.6). Compared to women with ER+/PR+ first tumors, those with ER-/PR- tumors had increased risk of CBC (RR = 1.4, 95% CI 1.1-1.7). Notably, women with ER-/PR- first tumors were more likely to develop CBC with the ER-/PR- phenotype (RR = 5.4, 95% CI 3.0-9.5), and risk remained elevated in multiple subgroups: BRCA1/2 mutation non-carriers, women younger than 45 years of age, women without a breast cancer family history, and women who were not treated with tamoxifen.

conclusionsHaving a hormone receptor negative first primary breast cancer is associated with increased risk of CBC. Women with ER-/PR- primary tumors were more likely to develop ER-/PR- CBC, even after excluding BRCA1/2 mutation carriers. Hormone receptor status, which is routinely evaluated in breast tumors, may be used clinically to determine treatment protocols and identify patients who may benefit from increased surveillance for CBC.

Indexed as

AdultAgedBRCA1 ProteinBRCA2 ProteinBreast NeoplasmsCase-Control StudiesFemaleHumansMiddle AgedMutationNeoplasm GradingNeoplasm StagingPopulation SurveillanceReceptors, EstrogenReceptors, ProgesteroneRisk FactorsBRCA1 ProteinBRCA2 ProteinReceptors, EstrogenReceptors, ProgesteroneContralateral breast cancerEstrogen receptorHormone receptorPopulation-basedProgesterone receptor

Identifiers

PMID28724391
PMCPMC5517810
OpenAlexW2737816050

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.