Evidence map›Paper›PMID 33736682›Full record

ArticleBreast cancer research : BCR2021

Risk factors for breast cancer development by tumor characteristics among women with benign breast disease.

Jonine D Figueroa, Gretchen L Gierach, Máire A Duggan, Shaoqi Fan, Ruth M Pfeiffer, Yihong Wang, Roni T Falk, Olivier Loudig, Mustapha Abubakar, Mindy Ginsberg and 4 more

Open access · goldAbstract read
In one paragraph

Article in Breast cancer research : BCR, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 25 papers.

0numbers the graph read from it
0cells of the map it votes in
25citing papers in PubMed
4.6field-weighted citation impact, top 5% 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

25 citing papers in PubMed, 42 citations in OpenAlex.

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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

14 authors at 6 institutions in 3 countries.

Jonine D Figueroa *National Cancer Institute, National Institutes of Health, Division of Cancer Epidemiology and Genetics, Bethesda, MD, USA. jonine.figueroa@ed.ac.uk.ORCID 0000-0002-5100-623X
Gretchen L Gierach *National Cancer Institute, National Institutes of Health, Division of Cancer Epidemiology and Genetics, Bethesda, MD, USA.
Máire A DugganDepartment of Pathology and Laboratory Medicine, Cumming School of Medicine, University of Calgary, Alberta, Calgary, Canada.
Shaoqi FanNational Cancer Institute, National Institutes of Health, Division of Cancer Epidemiology and Genetics, Bethesda, MD, USA.
Ruth M PfeifferNational Cancer Institute, National Institutes of Health, Division of Cancer Epidemiology and Genetics, Bethesda, MD, USA.
Yihong WangWarren Alpert Medical School of Brown University, Providence, RI, USA.
Roni T FalkNational Cancer Institute, National Institutes of Health, Division of Cancer Epidemiology and Genetics, Bethesda, MD, USA.
Olivier LoudigCenter for Discovery and Innovation (CDI), Hackensack Meridian Health, Nutley, NJ, USA.
Mustapha AbubakarNational Cancer Institute, National Institutes of Health, Division of Cancer Epidemiology and Genetics, Bethesda, MD, USA.
Mindy GinsbergAlbert Einstein College of Medicine, Jack and Pearl Resnick Campus, 1300 Morris Park Avenue, Belfer Building, Room 1301, Bronx, NY, 10461, USA.
Teresa M KimesKaiser Permanente Center for Health Research, Portland, OR, USA.
Kathryn Richert-BoeKaiser Permanente Center for Health Research, Portland, OR, USA.
Andrew G GlassKaiser Permanente Center for Health Research, Portland, OR, USA.
Thomas E RohanAlbert Einstein College of Medicine, Jack and Pearl Resnick Campus, 1300 Morris Park Avenue, Belfer Building, Room 1301, Bronx, NY, 10461, USA. thomas.rohan@einsteinmed.org.
National Institutes of Health · USKaiser Permanente Center for Health Research · USAlbert Einstein College of Medicine · USBrown University · USHackensack Meridian Health · USUniversity of Calgary · CA

Funding

Breast cancer research foundation BCRF-20-140Wellcome Trust 207800/Z/17/Z
6 · The paper itself

Abstract

backgroundAmong women diagnosed with invasive breast cancer, 30% have a prior diagnosis of benign breast disease (BBD). Thus, it is important to identify factors among BBD patients that elevate invasive cancer risk. In the general population, risk factors differ in their associations by clinical pathologic features; however, whether women with BBD show etiologic heterogeneity in the types of breast cancers they develop remains unknown.

methodsUsing a nested case-control study of BBD and breast cancer risk conducted in a community healthcare plan (Kaiser Permanente Northwest), we assessed relationships of histologic features in BBD biopsies and patient characteristics with subsequent breast cancer risk and tested for heterogeneity of associations by estrogen receptor (ER) status, tumor grade, and size. The study included 514 invasive breast cancer cases (median follow-up of 9 years post-BBD diagnosis) and 514 matched controls, diagnosed with proliferative or non-proliferative BBD between 1971 and 2006, with follow-up through mid-2015. Odds ratios (ORs) and 95% confidence intervals (CIs) were obtained using multivariable polytomous logistic regression models.

resultsBreast cancers were predominantly ER-positive (86%), well or moderately differentiated (73%), small (74% < 20 mm), and stage I/II (91%). Compared to patients with non-proliferative BBD, proliferative BBD with atypia conferred increased risk for ER-positive cancer (OR = 5.48, 95% CI = 2.14-14.01) with only one ER-negative case, P-heterogeneity = 0.45. The presence of columnar cell lesions (CCLs) at BBD diagnosis was associated with a 1.5-fold increase in the risk of both ER-positive and ER-negative tumors, with a 2-fold increase (95% CI = 1.21-3.58) observed among postmenopausal women (56%), independent of proliferative BBD status with and without atypia. We did not identify statistically significant differences in risk factor associations by tumor grade or size.

conclusionMost tumors that developed after a BBD diagnosis in this cohort were highly treatable low-stage ER-positive tumors. CCL in BBD biopsies may be associated with moderately increased risk, independent of BBD histology, and irrespective of ER status.

Indexed as

AdultAgedBiopsyBreastBreast DiseasesBreast NeoplasmsCase-Control StudiesCohort StudiesFemaleHumansHyperplasiaMiddle AgedOdds RatioReceptors, EstrogenRisk FactorsReceptors, EstrogenBenign breast diseaseBreast cancerColumnar cell lesionsEpidemiologyEstrogen receptorTumor characteristics

Identifiers

PMID33736682
PMCPMC7977564
OpenAlexW3127893352

What OpenQuestion holds

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LicenceCC BY
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Registered trials

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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.