Survival from breast cancer in women with a BRCA2 mutation by treatment.


Journal

British journal of cancer
ISSN: 1532-1827
Titre abrégé: Br J Cancer
Pays: England
ID NLM: 0370635

Informations de publication

Date de publication:
04 2021
Historique:
received: 14 07 2020
accepted: 29 10 2020
revised: 20 10 2020
pubmed: 19 2 2021
medline: 28 9 2021
entrez: 18 2 2021
Statut: ppublish

Résumé

The impact of various breast-cancer treatments on patients with a BRCA2 mutation has not been studied. We sought to estimate the impact of bilateral oophorectomy and other treatments on breast cancer-specific survival among patients with a germline BRCA2 mutation. We identified 664 women with stage I-III breast cancer and a BRCA2 mutation by combining five different datasets (retrospective and prospective). Subjects were followed for 7.2 years from diagnosis to death from breast cancer. Tumour characteristics and cancer treatments were patient-reported and derived from medical records. Predictors of survival were determined using Cox proportional hazard models, adjusted for other treatments and for prognostic features. The 10-year breast-cancer survival for ER-positive patients was 78.9% and for ER-negative patients was 82.3% (adjusted HR = 1.23 (95% CI, 0.62-2.45, p = 0.55)). The 10-year breast-cancer survival for women who had a bilateral oophorectomy was 89.1% and for women who did not have an oophorectomy was 59.0% (adjusted HR = 0.45; 95% CI, 0.28-0.72, p = 0.001). The adjusted hazard ratio for chemotherapy was 0.83 (95% CI, 0.65-1.53: p = 0.56). For women with breast cancer and a germline BRCA2 mutation, positive ER status does not predict superior survival. Oophorectomy is associated with a reduced risk of death from breast cancer and should be considered in the treatment plan.

Sections du résumé

BACKGROUND
The impact of various breast-cancer treatments on patients with a BRCA2 mutation has not been studied. We sought to estimate the impact of bilateral oophorectomy and other treatments on breast cancer-specific survival among patients with a germline BRCA2 mutation.
METHODS
We identified 664 women with stage I-III breast cancer and a BRCA2 mutation by combining five different datasets (retrospective and prospective). Subjects were followed for 7.2 years from diagnosis to death from breast cancer. Tumour characteristics and cancer treatments were patient-reported and derived from medical records. Predictors of survival were determined using Cox proportional hazard models, adjusted for other treatments and for prognostic features.
RESULTS
The 10-year breast-cancer survival for ER-positive patients was 78.9% and for ER-negative patients was 82.3% (adjusted HR = 1.23 (95% CI, 0.62-2.45, p = 0.55)). The 10-year breast-cancer survival for women who had a bilateral oophorectomy was 89.1% and for women who did not have an oophorectomy was 59.0% (adjusted HR = 0.45; 95% CI, 0.28-0.72, p = 0.001). The adjusted hazard ratio for chemotherapy was 0.83 (95% CI, 0.65-1.53: p = 0.56).
CONCLUSIONS
For women with breast cancer and a germline BRCA2 mutation, positive ER status does not predict superior survival. Oophorectomy is associated with a reduced risk of death from breast cancer and should be considered in the treatment plan.

Identifiants

pubmed: 33597716
doi: 10.1038/s41416-020-01164-1
pii: 10.1038/s41416-020-01164-1
pmc: PMC8076275
doi:

Substances chimiques

BRCA1 Protein 0
BRCA1 protein, human 0
BRCA2 Protein 0
BRCA2 protein, human 0
Biomarkers, Tumor 0
Receptors, Estrogen 0
Receptors, Progesterone 0
ERBB2 protein, human EC 2.7.10.1
Receptor, ErbB-2 EC 2.7.10.1

Types de publication

Journal Article Multicenter Study Research Support, N.I.H., Extramural Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

1524-1532

Subventions

Organisme : NCI NIH HHS
ID : R01 CA159868
Pays : United States

Investigateurs

Maria Błasińska-Morawiec (M)
Maria Chosia (M)
Kazimierz Drosik (K)
Sylwia Gozdecka-Grodecka (S)
Stanisław Goźdź (S)
Ewa Grzybowska (E)
Arkadiusz Jeziorski (A)
Aldona Karczewska (A)
Radzisław Kordek (R)
Agnieszka Synowiec (A)
Beata Kozak-Klonowska (B)
Katarzyna Lamperska (K)
Dariusz Lange (D)
Andrzej Mackiewicz (A)
Jerzy Władysław Mituś (JW)
Stanislas Niepsuj (S)
Oleg Oszurek (O)
Karol Gugała (K)
Zbigniew Morawiec (Z)
Tomasz Mierzwa (T)
Michał Posmyk (M)
Janusz Ryś (J)
Cezary Szczylik (C)
Michał Uciński (M)
Krzysztof Urbański (K)
Bernard Waśko (B)
Piotr Wandzel (P)
Michael Friedlander (M)
Sue Anne McLachlan (SA)
Stephanie Nesci (S)
Sandra Picken (S)
Sarah O'Connor (S)
Lucy Stanhope (L)
Andrea Eisen (A)
Kevin Sweet (K)
Raymond Kim (R)
William Foulkes (W)
Pal Moller (P)
Susan Neuhausen (S)
Carey Cullinane (C)
Charis Eng (C)
Peter Ainsworth (P)
Fergus Couch (F)
Christian Singer (C)
Beth Karlan (B)
Wendy McKinnon (W)
Marie Wood (M)

Commentaires et corrections

Type : ErratumIn

Références

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Auteurs

D Gareth Evans (DG)

Genomic Medicine, Manchester Academic Health Science Centre, The University of Manchester, Manchester, UK.

Kelly-Anne Phillips (KA)

Sir Peter MacCallum Department of Oncology, University of Melbourne, Parkville, Australia.
Department of Medical Oncology, Peter MacCallum Cancer Centre, Melbourne, Australia.
Centre for Epidemiology and Biostatistics, Melbourne School of Population and Global Health, The University of Melbourne, Melbourne, VIC, Australia.

Roger L Milne (RL)

Centre for Epidemiology and Biostatistics, Melbourne School of Population and Global Health, The University of Melbourne, Melbourne, VIC, Australia.
Precision Medicine, School of Clinical Sciences at Monash Health, Monash University, Clayton, VIC, Australia.
Cancer Epidemiology Division, Cancer Council Victoria, Melbourne, VIC, Australia.

Robert Fruscio (R)

Department of Medicine and Surgery, University of Milan-Bicocca, Milan, Italy.

Cezary Cybulski (C)

Department of Genetics and Pathology, International Hereditary Cancer Center, Pomeranian Medical University, Szczecin, Poland.

Jacek Gronwald (J)

Department of Genetics and Pathology, International Hereditary Cancer Center, Pomeranian Medical University, Szczecin, Poland.

Jan Lubinski (J)

Department of Genetics and Pathology, International Hereditary Cancer Center, Pomeranian Medical University, Szczecin, Poland.

Tomasz Huzarski (T)

Department of Genetics and Pathology, International Hereditary Cancer Center, Pomeranian Medical University, Szczecin, Poland.
University of Zielona Góra, Zielona Góra, Poland.

Zerin Hyder (Z)

Genomic Medicine, Manchester Academic Health Science Centre, The University of Manchester, Manchester, UK.

Claire Forde (C)

Genomic Medicine, Manchester Academic Health Science Centre, The University of Manchester, Manchester, UK.

Kelly Metcalfe (K)

Women's College Research Institute, Women's College Hospital, Toronto, ON, Canada.

Leigha Senter (L)

Division of Human Genetics, the Ohio State University Medical Center, Comprehensive Cancer Center, Columbus, OH, USA.

Jeffrey Weitzel (J)

Division of Clinical Cancer Genomics, Department of Population Sciences, City of Hope, Duarte, CA, USA.

Nadine Tung (N)

Beth Israel Deaconess Medical Center, Boston, MA, USA.

Dana Zakalik (D)

Nancy and James Grosfeld Cancer Genetics Center, Beaumont Cancer Institute, Beaumont Health, Royal Oak, MI, USA.

Maria Ekholm (M)

Manchester Academic Health Science Centre, Department of Medical Oncology, The Christie, Manchester, UK.

Ping Sun (P)

Women's College Research Institute, Women's College Hospital, Toronto, ON, Canada.

Steven A Narod (SA)

University of Zielona Góra, Zielona Góra, Poland. steven.narod@wchospital.ca.
Women's College Research Institute, Women's College Hospital, Toronto, ON, Canada. steven.narod@wchospital.ca.

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Classifications MeSH