Evidence map›Paper›PMID 38797791›Full record

ArticleBreast cancer research and treatment2024

Clinical breast exam contribution to breast cancer diagnosis in BRCA mutation carriers vs. average to intermediate risk women.

Tehillah S Menes, Douglas Zippel, Miri Sklair-Levy, Eitan Friedman, Rinat Bernstein-Molho, Renata Faermann, Dana Madorsky Feldman

Abstract read
In one paragraph

Article in Breast cancer research and treatment, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–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

1 citing paper in PubMed.

  1. Article
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

7 authors.

Tehillah S MenesDepartment of Surgery, Sheba Medical Center, Ramat Gan, Israel. Tehillah.menes@sheba.health.gov.il.ORCID http://orcid.org/0000-0001-7988-3747
Douglas ZippelDepartment of Surgery, Sheba Medical Center, Ramat Gan, Israel.
Miri Sklair-LevyMeirav Center for Women's Health and High-Risk Clinic, Sheba Medical Center, Ramat Gan, Israel.
Eitan FriedmanMeirav Center for Women's Health and High-Risk Clinic, Sheba Medical Center, Ramat Gan, Israel.
Rinat Bernstein-MolhoMeirav Center for Women's Health and High-Risk Clinic, Sheba Medical Center, Ramat Gan, Israel.
Renata FaermannMeirav Center for Women's Health and High-Risk Clinic, Sheba Medical Center, Ramat Gan, Israel.
Dana Madorsky FeldmanMeirav Center for Women's Health and High-Risk Clinic, Sheba Medical Center, Ramat Gan, Israel.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

purposeThe contribution of clinical breast exam (CBE) to breast cancer diagnosis in average risk women undergoing regular screening mammography is minimal. To evaluate the role of CBE in high-risk women, we compared BC diagnosis by CBE in BRCA mutation carriers undergoing regular BC surveillance to average to intermediate risk women undergoing regular breast cancer screening.

methodsA retrospective chart review of all consecutive screening visits of BRCA mutation carriers (January 2012-October 2022) and average to intermediate risk women (November 2016-December 2022) was completed. Women with histologically confirmed BC diagnosis were included. Additional CBE yield for BC diagnosis, defined as the percentage of all BC cases detected by CBE alone, was assessed in both groups.

resultsOverall, 12,997 CBEs were performed in 1,328 BRCA mutation carriers in whom 134 BCs were diagnosed. In 7,949 average to intermediate risk women who underwent 15,518 CBEs, 87 BCs were diagnosed. CBE contributed to BC diagnosis in 3 (2%) BRCA mutation carriers and 3 (4%) non-carriers. In both groups, over 4,000 CBEs were needed in order to diagnose one cancer. In all 3 BRCA mutation carriers BC was palpated during the surveillance round that did not include MRI. In the average to intermediate risk group, 2 of 3 cancers diagnosed following CBE findings were in a different location from the palpable finding.

conclusionsThe contribution of CBE to BC diagnosis is marginal for all women including BRCA mutation carriers. In BRCA mutation carriers, CBE appears redundant during the MRI surveillance round.

Indexed as

BRCA1 ProteinBRCA2 ProteinBreast NeoplasmsEarly Detection of CancerMammographyMutationAdultAgedFemaleGenetic Predisposition to DiseaseHeterozygoteHumansMiddle AgedRetrospective StudiesRisk FactorsBRCA1 ProteinBRCA1 protein, humanBRCA2 ProteinBRCA2 protein, humanBRCABreast cancerClinical breast examSurveillance

Identifiers

PMID38797791
PMCPMC11230960

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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.