Evidence map›Paper›PMID 41688965›Full record

ArticleBMC cancer2026

Breast cancer surgery in the era of genetic uncertainty: real-world outcomes in BRCA1/2 pathogenic variants and variants of uncertain significance.

Ilker Nihat Ökten, Tuba Baydaş, Sinan Koca, Mukaddes Feyza Baltacı, Filiz Özen, İbrahim Çil, Metin Eser, Adnan Gündoğdu, Merve Aktaş, Osman Cem Yılmaz

Abstract readMulticenter Study
In one paragraph

Article in BMC cancer, 2026. 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. Article
  2. 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

10 authors.

Ilker Nihat ÖktenDepartment of Medical Oncology, Göztepe Prof. Dr. Süleyman Yalçın City Hospital, Istanbul, Türkiye, Turkey. ilkernihat@gmail.com.
Tuba BaydaşDepartment of Medical Oncology, Göztepe Prof. Dr. Süleyman Yalçın City Hospital, Istanbul, Türkiye, Turkey.
Sinan KocaDepartment of Medical Oncology, Göztepe Prof. Dr. Süleyman Yalçın City Hospital, Istanbul, Türkiye, Turkey.
Mukaddes Feyza BaltacıDepartment of Medical Genetics, Göztepe Prof. Dr. Süleyman Yalçın City Hospital, Istanbul, Türkiye, Turkey.
Filiz ÖzenDepartment of Medical Genetics, Göztepe Prof. Dr. Süleyman Yalçın City Hospital, Istanbul, Türkiye, Turkey.
İbrahim ÇilDepartment of Medical Oncology, SBÜ Ümraniye Research and Training Hospital, Istanbul, Türkiye, Turkey.
Metin EserDepartment of Medical Genetics, SBÜ Ümraniye Research and Training Hospital, Istanbul, Türkiye, Turkey.
Adnan GündoğduDepartment of General Surgery, SBÜ Sancaktepe İlhan Varank Research and Training Hospital, Istanbul, Türkiye, Turkey.
Merve AktaşDepartment of General Surgery, Bayburt Public Hospital, Bayburt, Türkiye, Turkey.
Osman Cem YılmazDepartment of Breast Surgery, Istanbul Breast Center, Istanbul, Türkiye, Turkey.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundGermline testing for BRCA1 and BRCA2 has become integral to the management of breast cancer, with pathogenic variants strongly influencing surgical decision-making. However, the increasing detection of variants of uncertain significance (VUS) presents a major clinical challenge, as their implications for cancer risk and treatment remain unclear. This study aimed to evaluate real-world surgical management patterns among breast cancer patients carrying pathogenic BRCA1/2 variants or VUS, with a particular focus on determinants of final bilateral mastectomy.

methodsThis multicenter retrospective study included female breast cancer patients who underwent germline BRCA1/2 testing across three institutions in Türkiye between 2017 and 2025. Patients carrying pathogenic variants or VUS were identified and reclassified according to American College of Medical Genetics and Genomics (ACMG) criteria. Clinicopathological characteristics and surgical outcomes were compared between pathogenic and VUS groups. Final bilateral mastectomy was defined as either primary bilateral mastectomy or unilateral mastectomy followed by completion contralateral mastectomy. Multivariable logistic regression was performed to identify factors independently associated with final bilateral mastectomy, including a separate exploratory analysis restricted to VUS carriers.

resultsA total of 203 patients with abnormal BRCA results were included, comprising 107 pathogenic variant carriers and 96 VUS carriers. Patients with pathogenic BRCA variants were significantly younger at diagnosis and more frequently had triple-negative tumors. Final bilateral mastectomy was markedly more common among pathogenic variant carriers than VUS carriers (67% vs. 12%, p < 0.001). In multivariable analysis, pathogenic BRCA status remained independently associated with final bilateral mastectomy (adjusted OR 10.38, 95% CI 3.98-27.10; p < 0.001), while increasing age was also independently associated. Among VUS carriers, no clinicopathological variable-including molecular subtype, tumor size, Ki-67 index, family history, or BRCA1 versus BRCA2 VUS-was significantly associated with final bilateral mastectomy in univariate analyses. In exploratory multivariable modeling, younger age at diagnosis emerged as the only independent factor associated with surgical choice (adjusted OR per year 1.09, 95% CI 1.01-1.17; p = 0.027).

conclusionWhile pathogenic BRCA1/2 variants are strongly associated with bilateral mastectomy in breast cancer patients, surgical decision-making among VUS carriers appears largely independent of tumor biology or genetic subtype and is primarily influenced by age. These findings highlight substantial heterogeneity and potential overtreatment in the management of BRCA VUS carriers, underscoring the need for improved genetic counseling and standardized approaches to mitigate the impact of genetic uncertainty on clinical decision-making.

Indexed as

BRCA1 ProteinBRCA2 ProteinBreast NeoplasmsMastectomyAdultAgedFemaleGenetic Predisposition to DiseaseGenetic TestingGerm-Line MutationHumansMiddle AgedRetrospective StudiesUncertaintyBRCA1 ProteinBRCA1 protein, humanBRCA2 ProteinBRCA2 protein, humanBilateral mastectomyBRCA1 and BRCA2Breast cancerSurgical decision-makingVariants of uncertain significance

Identifiers

PMID41688965
PMCPMC13011663

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.