Incidence of endometrial cancer in BRCA mutation carriers.

BRCA Endometrial cancer Hysterectomy Prospective Tamoxifen

Journal

Gynecologic oncology
ISSN: 1095-6859
Titre abrégé: Gynecol Oncol
Pays: United States
ID NLM: 0365304

Informations de publication

Date de publication:
21 Aug 2024
Historique:
received: 15 05 2024
revised: 29 07 2024
accepted: 31 07 2024
medline: 22 8 2024
pubmed: 22 8 2024
entrez: 22 8 2024
Statut: aheadofprint

Résumé

Whether or not women who harbor a germline pathogenic variant ('mutation') in the BRCA1 or BRCA2 genes are at elevated risk of developing endometrial cancer is yet to be determined. We conducted a prospective analysis of 4959 BRCA mutation carriers with no prior history of cancer (except for breast or melanoma) and an intact uterus. After a mean of 6.7 years of follow-up there were 38 incident cases of endometrial cancer diagnosed; 30 among BRCA1 carriers and eight among BRCA2 carriers. The mean age at diagnosis was 58.4 years (range 46.8-76.1). The majority were of the endometrioid subtype (n = 16), followed by mixed endometroid and serous (n = 4), serous (n = 3) or clear cell (n = 1) (missing = 13). The cumulative incidence from age 40 to age 70 was 3.4% for BRCA1 carriers and was 1.6% for BRCA2 mutation carriers. Prior tamoxifen use was associated with a significant two-fold increased risk (HR = 2.24; 95% CI 1.10-4.55). There was no significant association between exogenous hormone use, oophorectomy, smoking or BMI at age 40 and risk (P ≥ 0.32). Compared to the general population, we observed higher rates of endometrial cancer among young BRCA1 mutation carriers; however, lifetime risks were similar. Women with prior tamoxifen exposure were at a significantly increased risk. These findings were based. on a small number of incident cases and require confirmation with additional follow-up of our aging cohort.

Identifiants

pubmed: 39173195
pii: S0090-8258(24)01052-7
doi: 10.1016/j.ygyno.2024.07.687
pii:
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

148-155

Informations de copyright

Copyright © 2024 Elsevier Inc. All rights reserved.

Déclaration de conflit d'intérêts

Declaration of competing interest All the authors declare that they have no conflict of interest.

Auteurs

Joanne Kotsopoulos (J)

Women's College Research Institute, Women's College Hospital, Toronto, ON, Canada; Dalla Lana School of Public Health, University of Toronto, Toronto, ON, Canada.

Jan Lubinski (J)

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

Tomasz Huzarski (T)

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

Brittany L Bychkovsky (BL)

Division of Cancer Genetics and Prevention, Dana-Farber Cancer Institute, Boston, MA, USA; Department of Medical Oncology, Dana-Farber Cancer Institute, Boston, MA, USA; Harvard Medical School, Boston, MA, USA.

Pal Moller (P)

Department of Tumour Biology, Institute of Cancer Research, The Norwegian Radium Hospital, 0379 Oslo, Norway.

Raymond H Kim (RH)

Division of Medical Oncology and Hematology, Princess Margaret Cancer Centre, Sinai Health System, Hospital for Sick Children, Ontario Institute for Cancer Research, Department of Medicine, University of Toronto, Canada.

Nadine Tung (N)

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

Andrea Eisen (A)

Toronto-Sunnybrook Regional Cancer Center, Toronto, ON, Canada.

William Foulkes (W)

McGill Program in Cancer Genetics, Department of Oncology, McGill University, Montreal, QC, Canada.

Christian F Singer (CF)

Department of Obstetrics and Gynecology and Comprehensive Cancer Center, Medical University of Vienna, Vienna, Austria.

Amber Aeilts (A)

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

Susan L Neuhausen (SL)

Department of Population Sciences, Beckman Research Institute of City of Hope, Duarte, CA, USA.

Louise Bordeleau (L)

Department of Oncology, McMaster University, Hamilton, ON, Canada.

Beth Karlan (B)

Department of Obstetrics and Gynecology, David Geffen School of Medicine, University of California Los Angeles, CA, USA.

Robert Fruscio (R)

Clinic of Obstetrics and Gynecology, IRCCS Fondazione San Gerardo dei Tintori, Monza, Italy.

Charis Eng (C)

Genomic Medicine Institute, Cleveland Clinic, Cleveland, OH, USA.

Olufunmilayo Olopade (O)

Department of Medicine and Human Genetics, University of Chicago, Chicago, IL, USA.

Dana Zakalik (D)

Cancer Genetics Program, Beaumont Hospital, Royal Oak, MI, USA.

Fergus Couch (F)

Division of Experimental Pathology and Laboratory Medicine, Department of Laboratory Medicine and Pathology, Mayo Clinic, Rochester, MN, USA.

Teresa Ramon Y Cajal (TR)

Familial Cancer Clinic, Medical Oncology, Hospital Santa Creu i Sant Pau, Barcelona, Spain.

Ping Sun (P)

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

Jacek Gronwald (J)

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

Steven A Narod (SA)

Women's College Research Institute, Women's College Hospital, Toronto, ON, Canada; Dalla Lana School of Public Health, University of Toronto, Toronto, ON, Canada. Electronic address: steven.narod@wchospital.ca.

Classifications MeSH