Evidence map›Paper›PMID 30496449›Full record

ArticleJournal of the National Cancer Institute2019

Risk-Reducing Oophorectomy and Breast Cancer Risk Across the Spectrum of Familial Risk.

Mary Beth Terry, Mary B Daly, Kelly Anne Phillips, Xinran Ma, Nur Zeinomar, Nicole Leoce, Gillian S Dite, Robert J MacInnis, Wendy K Chung, Julia A Knight and 11 more

Abstract read
In one paragraph

Article in Journal of the National Cancer Institute, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 26 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
26citing papers in PubMed, 1 pooled it
–field-weighted citation impact
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

26 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
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  15. Bilateral Salpingo-oophorectomy and Breast Cancer Risk forCancer prevention research (Philadelphia, Pa.) · 2021
    Review
  16. Article
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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

21 authors.

Mary Beth TerryDepartment of Epidemiology, Mailman School of Public Health, Columbia University, New York, NY.
Mary B DalyDepartment of Clinical Genetics, Fox Chase Cancer Center, Philadelphia, PA.
Kelly Anne PhillipsDepartment of Medical Oncology, Peter MacCallum Cancer Centre, Melbourne, Victoria, Australia.
Xinran MaDepartment of Epidemiology, Mailman School of Public Health, Columbia University, New York, NY.
Nur ZeinomarDepartment of Epidemiology, Mailman School of Public Health, Columbia University, New York, NY.
Nicole LeoceDepartment of Epidemiology, Mailman School of Public Health, Columbia University, New York, NY.
Gillian S DiteCentre for Epidemiology and Biostatistics, The University of Melbourne, Parkville, Victoria, Australia.
Robert J MacInnisCentre for Epidemiology and Biostatistics, The University of Melbourne, Parkville, Victoria, Australia.
Wendy K ChungHerbert Irving Comprehensive Cancer Center, Columbia University Medical Center, New York, NY.
Julia A KnightLunenfeld-Tanenbaum Research Institute, Sinai Health System, Toronto, Ontario, Canada.
Melissa C SoutheyGenetic Epidemiology Laboratory, Department of Pathology, The University of Melbourne, Parkville, Victoria, Australia.
Roger L MilneCentre for Epidemiology and Biostatistics, The University of Melbourne, Parkville, Victoria, Australia.
David GoldgarDepartment of Medicine and Huntsman Cancer Institute, University of Utah Health Sciences Center, Salt Lake City, UT.
Graham G GilesCancer Epidemiology and Intelligence Division, Cancer Council Victoria, Melbourne, Victoria, Australia.
Prue C WeidemanCentre for Epidemiology and Biostatistics, The University of Melbourne, Parkville, Victoria, Australia.
Gord GlendonLunenfeld-Tanenbaum Research Institute, Sinai Health System, Toronto, Ontario, Canada.
Richard BuchsbaumDepartment of Biostatistics, Mailman School of Public Health, Columbia University, New York, NY.
Irene L AndrulisLunenfeld-Tanenbaum Research Institute, Sinai Health System, Toronto, Ontario, Canada.
Esther M JohnDepartment of Medicine and Stanford Cancer Institute, Stanford University School of Medicine, Stanford, CA.
Saundra S BuysDepartment of Medicine and Huntsman Cancer Institute, University of Utah Health Sciences Center, Salt Lake City, UT.
John L HopperCentre for Epidemiology and Biostatistics, The University of Melbourne, Parkville, Victoria, Australia.

Funding

Core-001U01CA164920 · NCI · COLUMBIA UNIVERSITY HEALTH SCIENCES · PI Irene Andrulis, Sarah Violet Colonna · 2018 to 2026
$17.0M
Breast Cancer Family Registry CohortUM1CA164920 · NCI · CANCER PREVENTION INSTIT OF CALIFORNIA · PI ANDRULIS, IRENE, BUYS, SAUNDRA S · 2012 to 2017
$12.7M
Genes, environment and breast cancer risk: The 15 year follow-up of the Prof-SC (Diversity Supplement)R01CA159868 · NCI · COLUMBIA UNIVERSITY HEALTH SCIENCES · PI HOPPER, JOHN L, TERRY, MARY BETH · 2011 to 2015
$9.0M
NRSA Training CoreTL1TR001875 · NCATS · COLUMBIA UNIVERSITY HEALTH SCIENCES · PI SPANN, MARISA N, TAYLOR, JACQUELYN Y · 2016 to 2025
$8.9M
Training Program in Cancer-related Population SciencesT32CA094061 · NCI · COLUMBIA UNIVERSITY HEALTH SCIENCES · PI NEUGUT, ALFRED I., TERRY, MARY BETH · 2017 to 2021
$1.1M
NCATS NIH HHS TL1 TR001875NCI NIH HHS R01 CA159868NCI NIH HHS T32 CA094061NCI NIH HHS U01 CA164920NCI NIH HHS UM1 CA164920
6 · The paper itself

Abstract

There remains debate about whether risk-reducing salpingo-oophorectomy (RRSO), which reduces ovarian cancer risk, also reduces breast cancer risk. We examined the association between RRSO and breast cancer risk using a prospective cohort of 17 917 women unaffected with breast cancer at baseline (7.2% known carriers of BRCA1 or BRCA2 mutations). During a median follow-up of 10.7 years, 1046 women were diagnosed with incident breast cancer. Modeling RRSO as a time-varying exposure, there was no association with breast cancer risk overall (hazard ratio [HR] = 1.04, 95% confidence interval [CI] = 0.87 to 1.24) or by tertiles of predicted absolute risk based on family history (HR = 0.68, 95% CI = 0.32 to 1.47, HR = 0.94, 95% CI = 0.70 to 1.26, and HR = 1.10, 95% CI = 0.88 to 1.39, for lowest, middle, and highest tertile of risk, respectively) or for BRCA1 and BRCA2 mutation carriers when examined separately. There was also no association after accounting for hormone therapy use after RRSO. These findings suggest that RRSO should not be considered efficacious for reducing breast cancer risk.

Indexed as

Genetic Predisposition to DiseaseRisk Reduction BehaviorAdultBRCA1 ProteinBRCA2 ProteinBreast NeoplasmsFemaleFollow-Up StudiesHumansMiddle AgedMutationOvarian NeoplasmsOvariectomyPrognosisProspective StudiesBRCA1 ProteinBRCA1 protein, humanBRCA2 ProteinBRCA2 protein, human

Identifiers

PMID30496449
PMCPMC6410936

What OpenQuestion holds

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LicenceCC BY-NC
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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.