Evidence map›Paper›PMID 40016543›Full record

ArticleBreast cancer research and treatment2025

High risk surveillance MRI may not be necessary in BRCA1/2 mutation carriers over 70 years old.

Astrid Botty van den Bruele, Yi Ren, Samantha M Thomas, Koumani W Ntowe, Laura H Rosenberger, Carolyn Menendez, Lars J Grimm, Akiko Chiba, Jennifer K Plichta

Abstract read
In one paragraph

Article in Breast cancer research and treatment, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. RareOncology letters · 2026
    Article
  2. Monitoring Pharmacological Treatment of Breast Cancer with MRI.Current issues in molecular biology · 2025
    Review
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

9 authors.

Astrid Botty van den BrueleSurgical Oncology, Department of Surgery, Duke University, DUMC 3513, Durham, NC, 27710, USA. Astrid.Botty@duke.edu.ORCID http://orcid.org/0000-0002-0621-980X
Yi RenDuke Cancer Institute, Duke University, Durham, NC, USA.
Samantha M ThomasDuke Cancer Institute, Duke University, Durham, NC, USA.
Koumani W NtoweSurgical Oncology, Department of Surgery, Duke University, DUMC 3513, Durham, NC, 27710, USA.
Laura H RosenbergerSurgical Oncology, Department of Surgery, Duke University, DUMC 3513, Durham, NC, 27710, USA.
Carolyn MenendezSurgical Oncology, Department of Surgery, Duke University, DUMC 3513, Durham, NC, 27710, USA.
Lars J GrimmDuke Cancer Institute, Duke University, Durham, NC, USA.
Akiko ChibaSurgical Oncology, Department of Surgery, Duke University, DUMC 3513, Durham, NC, 27710, USA.
Jennifer K PlichtaSurgical Oncology, Department of Surgery, Duke University, DUMC 3513, Durham, NC, 27710, USA.

Funding

Women's Cancer Research ProgramP30CA014236 · NCI · DUKE UNIVERSITY · PI DONNA NIEDZWIECKI · 1985 to 2026
$174.8M
Building Interdisciplinary Research Careers in Women's Health (K12) - Administrative SupplementK12AR084231 · NIAMS · DUKE UNIVERSITY · PI Cindy Amundsen · 2023 to 2026
$2.5M
NCI NIH HHS P30 CA014236NIAMS NIH HHS K12 AR084231NIH HHS P30CA014236
6 · The paper itself

Abstract

backgroundThe risk of developing breast cancer up to age 80 for women with BRCA1/2 mutations is approximately 69-72%. The risk estimates, however, become labile in the later years of life. Many older BRCA1/2 mutation carriers who have not developed breast cancer continue to undergo high-risk surveillance. We evaluated breast cancers in women age ≥ 70 and identified which modality diagnosed the malignancy.

methodsFemales with BRCA1/2 mutations identified between 1996 and 2022 were included in this single institution retrospective review. The cohort was divided by age at BRCA1/2 diagnosis (30-59, 60-69 & ≥ 70). The number of malignancies and imaging modality which led to the diagnosis were recorded.

resultsThere were 316 patients with BRCA1/2 mutations: 266/316 (84.2%) were 30-59 years old at the time of genetic testing, 35/316 (11.1%) were 60-69, and 15/316 (4.7%) were ≥ 70. Median follow-up was 57 months (IQR 21.6-114.6). There were 178 (56.3%) breast malignancies diagnosed; 161/266 (60.5%) age 30-59, 11/35 (31.4%) ages 60-69, and 6/15 (40%) age ≥ 70 (p = 0.002). Of patients with a malignant diagnosis (n = 178), 140/178 (78.7%) had their cancers discovered on either screening or diagnostic mammogram, 30/178 (16.9%) by MRI, 1 /178 (0.6%) on ultrasound, and 1/178 (0.6%) was discovered on surgical pathology. Of the breast cancers diagnosed in patients age ≥ 70, 66.7% (4/6) were found on mammogram.

conclusionsIn women ≥ 70 with BRCA1/2 mutations, mammograms may be sufficient surveillance. Given that a number of older BRCA1/2 carriers may never develop breast cancer, our data supports individualized care and consideration for de-escalated surveillance in those ≥ 70.

Indexed as

BRCA1 ProteinBRCA2 ProteinBreast NeoplasmsMagnetic Resonance ImagingMutationAdultAgedAge FactorsEarly Detection of CancerFemaleGenes, BRCA1Genes, BRCA2Genetic Predisposition to DiseaseGenetic TestingHeterozygoteHumansBRCA1 ProteinBRCA1 protein, humanBRCA2 ProteinBRCA2 protein, humanBRCA1/BRCA2Breast CancerGenetic testingInvasive Ductal CarcinomaMutationOlder

Identifiers

PMID40016543
PMCPMC12318637

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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.