Evidence map›Paper›PMID 26565738›Full record

ArticleCancer2016

Breast cancer risk by extent and type of atypical hyperplasia: An update from the Nurses' Health Studies.

Laura C Collins, Sarah A Aroner, James L Connolly, Graham A Colditz, Stuart J Schnitt, Rulla M Tamimi

Open access · greenAbstract read
In one paragraph

Article in Cancer, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 23 papers.

0numbers the graph read from it
0cells of the map it votes in
23citing papers in PubMed
6.4field-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

23 citing papers in PubMed, 63 citations in OpenAlex.

  1. Review
  2. Review
  3. Observational
  4. An update on intraductal and intralobular proliferative lesions of the breast.Revista da Associacao Medica Brasileira (1992) · 2023
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  8. Automated Quantitative Measures of Terminal Duct Lobular Unit Involution and Breast Cancer Risk.Cancer epidemiology, biomarkers & prevention : a publication of the American Association for Cancer Research, cosponsored by the American Society of Preventive Oncology · 2020
    Article
  9. Article
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  11. The Regulatory Role of MicroRNAs in Breast Cancer.International journal of molecular sciences · 2019
    Review
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  13. Article
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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

6 authors at 4 institutions in 1 country.

Laura C CollinsDepartment of Pathology, Beth Israel Deaconess Medical Center and Harvard Medical School, Boston, Massachusetts.
Sarah A AronerDepartment of Nutrition, Harvard T. H. Chan School of Public Health, Boston, Massachusetts.
James L ConnollyDepartment of Pathology, Beth Israel Deaconess Medical Center and Harvard Medical School, Boston, Massachusetts.
Graham A ColditzInstitute of Public Health, Washington University School of Medicine, St. Louis, Missouri.
Stuart J SchnittDepartment of Pathology, Beth Israel Deaconess Medical Center and Harvard Medical School, Boston, Massachusetts.
Rulla M TamimiChanning Division of Network Medicine, Department of Medicine, Brigham and Women's Hospital, Boston, Massachusetts.
Beth Israel Deaconess Medical Center · USHarvard University · USBrigham and Women's Hospital · USMissouri Institute of Mental Health · US

Funding

Statistical MethodsP01CA087969 · NCI · BRIGHAM AND WOMEN'S HOSPITAL · PI TWOROGER, SHELLEY S · 2000 to 2019
$77.8M
Risk Factors for Breast Cancer in Younger NursesR01CA050385 · NCI · HARVARD UNIVERSITY (SCH OF PUBLIC HLTH) · PI ELIASSEN, A. HEATHER, WILLETT, WALTER C. · 1989 to 2019
$32.3M
Long Term Multidisciplinary Study of Cancer in Women: The Nurses Health StudyUM1CA186107 · NCI · BRIGHAM AND WOMEN'S HOSPITAL · PI ELIASSEN, A. HEATHER, STAMPFER, MEIR · 2014 to 2023
$22.3M
Life Course Cancer Epidemiology Cohort in WomenUM1CA176726 · NCI · HARVARD SCHOOL OF PUBLIC HEALTH · PI WILLETT, WALTER C. · 2013 to 2017
$15.7M
BENIGN BREAST DISEASE &RISK OF BREAST CANCERR01CA046475 · NCI · BRIGHAM AND WOMEN'S HOSPITAL · PI TAMIMI, RULLA M · 1987 to 2009
$3.1M
Computational pathology to predict breast cancer risk in benign breast diseaseR21CA187642 · NCI · BETH ISRAEL DEACONESS MEDICAL CENTER · PI SCHNITT, STUART, TAMIMI, RULLA M · 2015 to 2016
$439k
NCI NIH HHS CA046475NCI NIH HHS CA050385NCI NIH HHS CA087969NCI NIH HHS CA187642NCI NIH HHS P01 CA087969NCI NIH HHS R01 CA046475NCI NIH HHS R01 CA050385NCI NIH HHS R21 CA187642NCI NIH HHS UM1 CA176726NCI NIH HHS UM1CA176726NCI NIH HHS UM1 CA186107
6 · The paper itself

Abstract

backgroundWomen with atypical hyperplasia (AH) on a benign breast biopsy specimen are at increased risk for the development of breast cancer. However, the relation between the type and extent of AH (atypical ductal hyperplasia [ADH] vs atypical lobular hyperplasia [ALH]) and the magnitude of the breast cancer risk is not well defined.

methodsA nested case-control study of benign breast disease and breast cancer risk was conducted. Women with breast cancer and prior benign breast biopsy findings (488 cases) were matched to women with prior benign breast biopsy findings who were free from breast cancer (1907 controls). Benign breast biopsy slides were reviewed and categorized as nonproliferative, proliferative without atypia, or AH (ADH or ALH). The number of foci of AH was also recorded.

resultsAmong women with ADH, the interrelation between the extent of atypia and breast cancer risk was not significant (odds ratio [OR] for 1 or 2 foci, 3.5; 95% confidence interval [CI], 2.2-5.6; OR for ≥3 foci, 2.7; 95% CI, 1.4-5.1; P = .41). Similarly, although the risk with ALH was higher for those with ≥3 foci than for those with <3 foci, the difference was not statistically significant (OR for 1 or 2 foci, 5.2; 95% CI, 2.7-10.0; OR for ≥3 foci, 8.0; 95% CI, 4.5-14.2; P = .19).

conclusionsThis analysis demonstrates that the extent of ADH or ALH does not significantly contribute to breast cancer risk. The lack of a significant dose-response relation between the extent and type of atypia and breast cancer risk suggests that it would be premature to use the extent of atypia to influence management decisions for women with ADH or ALH.

Indexed as

AdolescentAdultAgedBiopsyBreastBreast NeoplasmsCase-Control StudiesCohort StudiesFemaleHumansHyperplasiaMiddle AgedOdds RatioProspective StudiesRisk FactorsYoung Adultatypical hyperplasiabenign breast diseasebreast cancer

Identifiers

PMID26565738
PMCPMC4742394
OpenAlexW2175560280

What OpenQuestion holds

Textmetadata
LicenceTDM
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.