Survival after bilateral risk-reducing mastectomy in healthy BRCA1 and BRCA2 mutation carriers.


Journal

Breast cancer research and treatment
ISSN: 1573-7217
Titre abrégé: Breast Cancer Res Treat
Pays: Netherlands
ID NLM: 8111104

Informations de publication

Date de publication:
Oct 2019
Historique:
received: 27 05 2019
accepted: 02 07 2019
pubmed: 16 7 2019
medline: 12 2 2020
entrez: 15 7 2019
Statut: ppublish

Résumé

In healthy BRCA1/2 mutation carriers, bilateral risk-reducing mastectomy (BRRM) strongly reduces the risk of developing breast cancer (BC); however, no clear survival benefit of BRRM over BC surveillance has been reported yet. In this Dutch multicenter cohort study, we used multivariable Cox models with BRRM as a time-dependent covariable to estimate the associations between BRRM and the overall and BC-specific mortality rates, separately for BRCA1 and BRCA2 mutation carriers. During a mean follow-up of 10.3 years, 722 out of 1712 BRCA1 (42%) and 406 out of 1145 BRCA2 (35%) mutation carriers underwent BRRM. For BRCA1 mutation carriers, we observed 52 deaths (20 from BC) in the surveillance group, and 10 deaths (one from BC) after BRRM. The hazard ratios were 0.40 (95% CI 0.20-0.90) for overall mortality and 0.06 (95% CI 0.01-0.46) for BC-specific mortality. BC-specific survival at age 65 was 93% for surveillance and 99.7% for BRRM. For BRCA2 mutation carriers, we observed 29 deaths (7 from BC) in the surveillance group, and 4 deaths (no BC) after BRRM. The hazard ratio for overall mortality was 0.45 (95% CI 0.15-1.36). BC-specific survival at age 65 was 98% for surveillance and 100% for BRRM. BRRM was associated with lower mortality than surveillance for BRCA1 mutation carriers, but for BRCA2 mutation carriers, BRRM may lead to similar BC-specific survival as surveillance. Our findings support a more individualized counseling based on BRCA mutation type.

Sections du résumé

BACKGROUND BACKGROUND
In healthy BRCA1/2 mutation carriers, bilateral risk-reducing mastectomy (BRRM) strongly reduces the risk of developing breast cancer (BC); however, no clear survival benefit of BRRM over BC surveillance has been reported yet.
METHODS METHODS
In this Dutch multicenter cohort study, we used multivariable Cox models with BRRM as a time-dependent covariable to estimate the associations between BRRM and the overall and BC-specific mortality rates, separately for BRCA1 and BRCA2 mutation carriers.
RESULTS RESULTS
During a mean follow-up of 10.3 years, 722 out of 1712 BRCA1 (42%) and 406 out of 1145 BRCA2 (35%) mutation carriers underwent BRRM. For BRCA1 mutation carriers, we observed 52 deaths (20 from BC) in the surveillance group, and 10 deaths (one from BC) after BRRM. The hazard ratios were 0.40 (95% CI 0.20-0.90) for overall mortality and 0.06 (95% CI 0.01-0.46) for BC-specific mortality. BC-specific survival at age 65 was 93% for surveillance and 99.7% for BRRM. For BRCA2 mutation carriers, we observed 29 deaths (7 from BC) in the surveillance group, and 4 deaths (no BC) after BRRM. The hazard ratio for overall mortality was 0.45 (95% CI 0.15-1.36). BC-specific survival at age 65 was 98% for surveillance and 100% for BRRM.
CONCLUSION CONCLUSIONS
BRRM was associated with lower mortality than surveillance for BRCA1 mutation carriers, but for BRCA2 mutation carriers, BRRM may lead to similar BC-specific survival as surveillance. Our findings support a more individualized counseling based on BRCA mutation type.

Identifiants

pubmed: 31302855
doi: 10.1007/s10549-019-05345-2
pii: 10.1007/s10549-019-05345-2
pmc: PMC6745043
doi:

Substances chimiques

BRCA1 Protein 0
BRCA1 protein, human 0
BRCA2 Protein 0
BRCA2 protein, human 0

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

723-733

Subventions

Organisme : Dutch Pink Ribbon foundation
ID : 2016-209

Commentaires et corrections

Type : CommentIn
Type : CommentIn

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Auteurs

Bernadette A M Heemskerk-Gerritsen (BAM)

Department of Medical Oncology, Erasmus MC Cancer Institute, PO Box 5201, 3008 AE, Rotterdam, The Netherlands. b.heemskerk-gerritsen@erasmusmc.nl.

Agnes Jager (A)

Department of Medical Oncology, Erasmus MC Cancer Institute, PO Box 5201, 3008 AE, Rotterdam, The Netherlands.

Linetta B Koppert (LB)

Department of Surgery, Erasmus MC Cancer Institute, Rotterdam, The Netherlands.

A Inge-Marie Obdeijn (AI)

Department of Radiology, Erasmus MC Cancer Institute, Rotterdam, The Netherlands.

Margriet Collée (M)

Department of Clinical Genetics, Erasmus MC Cancer Institute, Rotterdam, The Netherlands.

Hanne E J Meijers-Heijboer (HEJ)

Department of Clinical Genetics, Academic Medical Center, Amsterdam, The Netherlands.

Denise J Jenner (DJ)

Department of Epidemiology, Netherlands Cancer Institute-Antoni van Leeuwenhoek Hospital, Amsterdam, The Netherlands.

Hester S A Oldenburg (HSA)

Department of Surgery, Netherlands Cancer Institute, Amsterdam, The Netherlands.

Klaartje van Engelen (K)

Department of Clinical Genetics, VU University Medical Center, Amsterdam, The Netherlands.

Jakob de Vries (J)

Department of Surgery, University Medical Center Groningen, Groningen, The Netherlands.

Christi J van Asperen (CJ)

Department of Clinical Genetics, Leiden University Medical Center, Leiden, The Netherlands.

Peter Devilee (P)

Department of Human Genetics, Leiden University Medical Center, Leiden, The Netherlands.

Marinus J Blok (MJ)

Department of Clinical Genetics, Maastricht University Medical Center, Maastricht, The Netherlands.

C Marleen Kets (CM)

Department of Human Genetics, Radboud University Medical Center, Nijmegen, The Netherlands.

Margreet G E M Ausems (MGEM)

Department of Medical Genetics, University Medical Center Utrecht, Utrecht, The Netherlands.

Caroline Seynaeve (C)

Department of Medical Oncology, Erasmus MC Cancer Institute, PO Box 5201, 3008 AE, Rotterdam, The Netherlands.

Matti A Rookus (MA)

Department of Epidemiology, Netherlands Cancer Institute-Antoni van Leeuwenhoek Hospital, Amsterdam, The Netherlands.

Maartje J Hooning (MJ)

Department of Medical Oncology, Erasmus MC Cancer Institute, PO Box 5201, 3008 AE, Rotterdam, The Netherlands.

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Classifications MeSH