# Oncological safety and preventive impact of nipple-sparing mastectomy in patients with BRCA1/2 mutation: multicentre study of the Korea Robot-endoscopy Minimal Access Breast Surgery Study Group (KoREa-BSG)

**Authors:** Hong-Kyu Kim, Dong Seung Shin, Sung Yoon Jang, Soong June Bae, Eun Young Kim, Chihwan David Cha, Hyung Seok Park, Jeeyeon Lee, Jun-Hee Lee, Eun-Shin Lee, Jung Eun Choi, Soo Youn Bae, Hee-Chul Shin, Dongwon Kim, Moo Hyun Lee, Yong-Yeup Kim, Sang-Ah Han, Janghee Lee, Young Woo Chang, Junwon Min, Sanghwa Kim, Young-Joon Kang, Hee Jun Choi, Sae Byul Lee, Jai Min Ryu, Joo Heung Kim, Joo Heung Kim, Beom Seok Ko, Ku Sang Kim, Young Jin Choi, Hye Yoon Lee, Sang Eun Nam, Zisun Kim, Jong Eun Lee, Eunhwa Park, Hyuk Jai Shin, Min Kyoon Kim, Seong Uk Kwon, Jeea Lee, Jee Ye Kim

PMC · DOI: 10.1093/bjsopen/zraf168 · BJS Open · 2026-02-17

## TL;DR

Nipple-sparing mastectomy is a safe and effective option for BRCA1/2 mutation carriers, with similar recurrence rates and reduced risk of contralateral breast cancer.

## Contribution

Demonstrates NSM's oncological safety and preventive impact in BRCA1/2 carriers, particularly in Asian populations.

## Key findings

- Ipsilateral local recurrence rates were similar between BRCA1/2 carriers and non-carriers.
- Contralateral breast cancer occurred in 4.5% of BRCA1/2 carriers who did not undergo risk-reducing NSM.
- No contralateral breast cancer cases were observed in patients who underwent risk-reducing NSM.

## Abstract

Nipple-sparing mastectomy (NSM) is a surgical option offering both oncological safety and cosmetic benefits. However, the oncological safety of NSM in carriers of BRCA1/2 pathogenic variants/likely pathogenic variants (PV/LPV) with breast cancer and the role of risk-reducing mastectomy remain underexplored, especially in Asian populations. This study evaluated the safety and effectiveness of NSM in BRCA1/2 PV/LPV carriers and assessed the preventive impact of contralateral risk-reducing NSM (RRNSM) on cancer incidence.

This multicentre retrospective study included women aged 20–80 years who underwent NSM for therapeutic or risk-reducing purposes and received germline BRCA1/2 tests between May 2006 and June 2022 across 19 institutions in Korea. Patients with distant metastasis at diagnosis were excluded. Information on demographics, the clinical characteristics of patients and tumours, surgical details, and follow-up outcomes was collected from a review the medical records of each participating institution. The primary outcome was the oncological safety of NSM, assessed by comparing ipsilateral local recurrence rates between patients with and without BRCA1/2 PV/LPV. The secondary outcome was cancer incidence in patients who underwent contralateral RRNSM versus those who did not.

In all, 787 women underwent 906 NSMs, with a median (interquartile range) follow-up of 59.3 (44.0–82.8) months. Among the participants, 186 (23.6%) were BRCA1/2 PV/LPV carriers. Ipsilateral local recurrence rates were comparable between BRCA1/2 PV/LPV carriers and non-carriers (6.4 versus 7.4%, respectively). The 5-year local recurrence-free survival rates did not differ significantly between BRCA1/2 PV/LPV carriers and non-carriers (92.2% versus 93.2%, respectively; P = 0.87). Contralateral breast cancer occurred in 4.5% of patients with BRCA1/2 PV/LPV who did not undergo contralateral RRNSM, whereas no cases of contralateral breast cancer were reported among patients who underwent RRNSM regardless of BRCA1/2 status.

This study highlights NSM as a safe and effective surgical option for BRCA1/2 PV/LPV carriers with breast cancer, as well as a risk-reducing strategy. Further prospective studies are needed to confirm these findings and evaluate long-term outcomes.

This multicentre study evaluated the oncological safety and preventive potential of nipple-sparing mastectomy (NSM) in carriers of BRCA1/2 mutations. NSM had comparable local recurrence rates to traditional mastectomy and a reduced incidence of contralateral breast cancer, supporting its role as a viable surgical option for high-risk breast cancer patients.

## Linked entities

- **Genes:** BRCA1 (BRCA1 DNA repair associated) [NCBI Gene 672], BRCA2 (BRCA2 DNA repair associated) [NCBI Gene 675]
- **Diseases:** breast cancer (MONDO:0004989)

## Full-text entities

- **Genes:** BRCA2 (BRCA2 DNA repair associated) [NCBI Gene 675] {aka BRCC2, BROVCA2, FACD, FAD, FAD1, FANCD}, ERBB2 (erb-b2 receptor tyrosine kinase 2) [NCBI Gene 2064] {aka CD340, HER-2, HER-2/neu, HER2, MLN 19, MLN-19}, BRCA1 (BRCA1 DNA repair associated) [NCBI Gene 672] {aka BRCAI, BRCC1, BROVCA1, FANCS, IRIS, PNCA4}, NR4A1 (nuclear receptor subfamily 4 group A member 1) [NCBI Gene 3164] {aka GFRP1, HMR, N10, NAK-1, NGFIB, NP10}
- **Diseases:** NSM (MESH:C000626393), Breast Cancer (MESH:D001943), triple-negative breast cancer (MESH:D064726), PV (MESH:D008881), triple (MESH:C536008), LPV (MESH:C537419), RRM (MESH:D000072656), metastasis (MESH:D009362), T (MESH:D001260), DCIS (MESH:D002285), benign tumours (MESH:D009369)
- **Chemicals:** LPV (-)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

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## Figures

2 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12911035/full.md

## References

40 references — full list in the complete paper: https://tomesphere.com/paper/PMC12911035/full.md

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Source: https://tomesphere.com/paper/PMC12911035