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Incidence of endometrial cancer in BRCA mutation carriers.
Kotsopoulos, Joanne; Lubinski, Jan; Huzarski, Tomasz; Bychkovsky, Brittany L; Moller, Pal; Kim, Raymond H; Tung, Nadine; Eisen, Andrea; Foulkes, William; Singer, Christian F; Aeilts, Amber; Neuhausen, Susan L; Bordeleau, Louise; Karlan, Beth; Fruscio, Robert; Eng, Charis; Olopade, Olufunmilayo; Zakalik, Dana; Couch, Fergus; Y Cajal, Teresa Ramon; Sun, Ping; Gronwald, Jacek; Narod, Steven A.
Affiliation
  • 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.
  • Lubinski J; International Hereditary Cancer Center, Department of Genetics and Pathology, Pomeranian Medical University, Szczecin, Poland.
  • Huzarski T; International Hereditary Cancer Center, Department of Genetics and Pathology, Pomeranian Medical University, Szczecin, Poland.
  • 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.
  • Moller P; Department of Tumour Biology, Institute of Cancer Research, The Norwegian Radium Hospital, 0379 Oslo, Norway.
  • 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.
  • Tung N; Beth Israel Deaconess Medical Center, Boston, MA, USA.
  • Eisen A; Toronto-Sunnybrook Regional Cancer Center, Toronto, ON, Canada.
  • Foulkes W; McGill Program in Cancer Genetics, Department of Oncology, McGill University, Montreal, QC, Canada.
  • Singer CF; Department of Obstetrics and Gynecology and Comprehensive Cancer Center, Medical University of Vienna, Vienna, Austria.
  • Aeilts A; Division of Human Genetics, the Ohio State University Medical Center, Comprehensive Cancer Center, Columbus, OH, USA.
  • Neuhausen SL; Department of Population Sciences, Beckman Research Institute of City of Hope, Duarte, CA, USA.
  • Bordeleau L; Department of Oncology, McMaster University, Hamilton, ON, Canada.
  • Karlan B; Department of Obstetrics and Gynecology, David Geffen School of Medicine, University of California Los Angeles, CA, USA.
  • Fruscio R; Clinic of Obstetrics and Gynecology, IRCCS Fondazione San Gerardo dei Tintori, Monza, Italy.
  • Eng C; Genomic Medicine Institute, Cleveland Clinic, Cleveland, OH, USA.
  • Olopade O; Department of Medicine and Human Genetics, University of Chicago, Chicago, IL, USA.
  • Zakalik D; Cancer Genetics Program, Beaumont Hospital, Royal Oak, MI, USA.
  • Couch F; Division of Experimental Pathology and Laboratory Medicine, Department of Laboratory Medicine and Pathology, Mayo Clinic, Rochester, MN, USA.
  • Y Cajal TR; Familial Cancer Clinic, Medical Oncology, Hospital Santa Creu i Sant Pau, Barcelona, Spain.
  • Sun P; Women's College Research Institute, Women's College Hospital, Toronto, ON, Canada.
  • Gronwald J; International Hereditary Cancer Center, Department of Genetics and Pathology, Pomeranian Medical University, Szczecin, Poland.
  • 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.
Gynecol Oncol ; 189: 148-155, 2024 Oct.
Article in En | MEDLINE | ID: mdl-39173195
ABSTRACT

OBJECTIVE:

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.

METHODS:

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.

RESULTS:

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).

CONCLUSIONS:

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.
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Endometrial Neoplasms / Genes, BRCA1 Limits: Adult / Aged / Female / Humans / Middle aged Language: En Journal: Gynecol Oncol Year: 2024 Type: Article Affiliation country: Canada

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Endometrial Neoplasms / Genes, BRCA1 Limits: Adult / Aged / Female / Humans / Middle aged Language: En Journal: Gynecol Oncol Year: 2024 Type: Article Affiliation country: Canada