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Bilateral Oophorectomy and All-Cause Mortality in Women With BRCA1 and BRCA2 Sequence Variations.
Kotsopoulos, Joanne; Gronwald, Jacek; Huzarski, Tomasz; Møller, Pål; Pal, Tuya; McCuaig, Jeanna M; Singer, Christian F; Karlan, Beth Y; Aeilts, Amber; Eng, Charis; Eisen, Andrea; Bordeleau, Louise; Foulkes, William D; Tung, Nadine; Couch, Fergus J; Fruscio, Robert; Neuhausen, Susan L; Zakalik, Dana; Cybulski, Cezary; Metcalfe, Kelly; Olopade, Olufunmilayo I; Sun, Ping; Lubinski, Jan; Narod, Steven A.
Afiliação
  • Kotsopoulos J; Women's College Research Institute, University of Toronto, Toronto, Ontario, Canada.
  • Gronwald J; Dalla Lana School of Public Health, University of Toronto, Toronto, Ontario, Canada.
  • Huzarski T; International Hereditary Cancer Center, Department of Genetics and Pathology, Pomeranian Medical University, Szczecin, Poland.
  • Møller P; International Hereditary Cancer Center, Department of Genetics and Pathology, Pomeranian Medical University, Szczecin, Poland.
  • Pal T; Department of Tumour Biology, The Norwegian Radium Hospital, Oslo University Hospital, Oslo, Norway.
  • McCuaig JM; Vanderbilt-Ingram Cancer Center, Department of Medicine, Vanderbilt University Medical Center, Nashville, Tennessee.
  • Singer CF; Princess Margaret Cancer Centre, University Health Network, Toronto, Ontario, Canada.
  • Karlan BY; Department of Molecular Genetics, University of Toronto, Toronto, Ontario, Canada.
  • Aeilts A; Department of Obstetrics and Gynecology and Comprehensive Cancer Center, Medical University of Vienna, Vienna, Austria.
  • Eng C; Department of Obstetrics and Gynecology, David Geffen School of Medicine, University of California, Los Angeles.
  • Eisen A; Comprehensive Cancer Center, Division of Human Genetics, The Ohio State University Medical Center, Columbus.
  • Bordeleau L; Genomic Medicine Institute and Center for Personalized Genetic Healthcare, Cleveland Clinic, Cleveland, Ohio.
  • Foulkes WD; Sunnybrook Odette Cancer Center, Department of Medical Oncology, University of Toronto, Toronto, Ontario, Canada.
  • Tung N; Department of Oncology, Juravinski Cancer Centre and McMaster University, Hamilton, Ontario, Canada.
  • Couch FJ; McGill Program in Cancer Genetics, Department of Oncology, McGill University, Montreal, Quebec, Canada.
  • Fruscio R; Cancer Risk and Prevention Program, Beth Israel Deaconess Medical Center, Boston, Massachusetts.
  • Neuhausen SL; Division of Experimental Pathology and Laboratory Medicine, Department of Laboratory Medicine and Pathology, Mayo Clinic, Rochester, Minnesota.
  • Zakalik D; Clinic of Obstetrics and Gynecology, Department of Medicine and Surgery, University of Milano-Bicocca, Monza, Italy.
  • Cybulski C; Department of Population Sciences, Beckman Research Institute of City of Hope, Duarte, California.
  • Metcalfe K; Grosfeld Cancer Genetics Center, Beaumont Health, Oakland University William Beaumont School of Medicine, Royal Oak, Michigan.
  • Olopade OI; International Hereditary Cancer Center, Department of Genetics and Pathology, Pomeranian Medical University, Szczecin, Poland.
  • Sun P; Women's College Research Institute, University of Toronto, Toronto, Ontario, Canada.
  • Lubinski J; Bloomberg School of Nursing, University of Toronto, Toronto, Ontario, Canada.
  • Narod SA; Department of Medicine and Human Genetics, University of Chicago, Chicago, Illinois.
JAMA Oncol ; 10(4): 484-492, 2024 Apr 01.
Article em En | MEDLINE | ID: mdl-38421677
ABSTRACT
Importance Preventive bilateral salpingo-oophorectomy is offered to women at high risk of ovarian cancer who carry a pathogenic variant in BRCA1 or BRCA2; however, the association of oophorectomy with all-cause mortality has not been clearly defined.

Objective:

To evaluate the association between bilateral oophorectomy and all-cause mortality among women with a BRCA1 or BRCA2 sequence variation. Design, Setting, and

Participants:

In this international, longitudinal cohort study of women with BRCA sequence variations, information on bilateral oophorectomy was obtained via biennial questionnaire. Participants were women with a BRCA1 or BRCA2 sequence variation, no prior history of cancer, and at least 1 follow-up questionnaire completed. Women were followed up from age 35 to 75 years for incident cancers and deaths. Cox proportional hazards regression was used to estimate the hazard ratios (HRs) and 95% CIs for all-cause mortality associated with a bilateral oophorectomy (time dependent). Data analysis was performed from January 1 to June 1, 2023. Exposures Self-reported bilateral oophorectomy (with or without salpingectomy). Main Outcomes and

Measures:

All-cause mortality, breast cancer-specific mortality, and ovarian cancer-specific mortality.

Results:

There were 4332 women (mean age, 42.6 years) enrolled in the cohort, of whom 2932 (67.8%) chose to undergo a preventive oophorectomy at a mean (range) age of 45.4 (23.0-77.0) years. After a mean follow-up of 9.0 years, 851 women had developed cancer and 228 had died; 57 died of ovarian or fallopian tube cancer, 58 died of breast cancer, 16 died of peritoneal cancer, and 97 died of other causes. The age-adjusted HR for all-cause mortality associated with oophorectomy was 0.32 (95% CI, 0.24-0.42; P < .001). The age-adjusted HR was 0.28 (95% CI, 0.20-0.38; P < .001) and 0.43 (95% CI, 0.22-0.90; P = .03) for women with BRCA1 and BRCA2 sequence variations, respectively. For women with BRCA1 sequence variations, the estimated cumulative all-cause mortality to age 75 years for women who had an oophorectomy at age 35 years was 25%, compared to 62% for women who did not have an oophorectomy. For women with BRCA2 sequence variations, the estimated cumulative all-cause mortality to age 75 years was 14% for women who had an oophorectomy at age 35 years compared to 28% for women who did not have an oophorectomy. Conclusions and Relevance In this cohort study among women with a BRCA1 or BRCA2 sequence variation, oophorectomy was associated with a significant reduction in all-cause mortality.
Assuntos

Texto completo: 1 Coleções: 01-internacional Contexto em Saúde: 6_ODS3_enfermedades_notrasmisibles Base de dados: MEDLINE Assunto principal: Neoplasias Ovarianas / Neoplasias da Mama Limite: Adult / Aged / Female / Humans / Middle aged Idioma: En Revista: JAMA Oncol / JAMA oncol. (Online) / JAMA oncology (Online) Ano de publicação: 2024 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Contexto em Saúde: 6_ODS3_enfermedades_notrasmisibles Base de dados: MEDLINE Assunto principal: Neoplasias Ovarianas / Neoplasias da Mama Limite: Adult / Aged / Female / Humans / Middle aged Idioma: En Revista: JAMA Oncol / JAMA oncol. (Online) / JAMA oncology (Online) Ano de publicação: 2024 Tipo de documento: Article