High-Grade Serous Carcinoma at Risk-Reducing Salpingo-Oophorectomy in Asymptomatic Carriers of BRCA1/2 Pathogenic Variants: Prevalence and Clinical Factors

Author:

Stroot Iris A.S.12ORCID,Brouwer Jan1,Bart Joost3ORCID,Hollema Harry3,Stommel-Jenner Denise J.4,Wagner Marise M.1,van Doorn Helena C.5ORCID,de Hullu Joanne A.6,Gaarenstroom Katja N.7ORCID,Beurden Marc8,van Lonkhuijzen Luc R.C.W.9ORCID,Slangen Brigitte F.M.10,Zweemer Ronald P.11ORCID,Gómez Garcia Encarna B.12ORCID,Ausems Margreet G.E.M.13ORCID,Boere Ingrid A.14,van Engelen Klaartje15,van Asperen Christi J.16ORCID,Schmidt Marjanka K.41617ORCID,Wevers Marijke R.18ORCID,de Bock Geertruida H.2ORCID,Mourits Marian J.E.119ORCID,

Affiliation:

1. Department of Obstetrics and Gynecology, University Medical Center Groningen, University of Groningen, Groningen, the Netherlands

2. Department of Epidemiology, University Medical Center Groningen, University of Groningen, Groningen, the Netherlands

3. Department of Pathology, University Medical Center Groningen, University of Groningen, Groningen, the Netherlands

4. Department of Epidemiology, Netherlands Cancer Institute, Amsterdam, the Netherlands

5. Department of Gynecologic Oncology, Erasmus MC Cancer Institute, University Medical Center Rotterdam, Rotterdam, the Netherlands

6. Department of Obstetrics and Gynecology, Radboud University Medical Center, Nijmegen, the Netherlands

7. Department of Obstetrics and Gynecology, Leiden University Medical Center, Leiden, the Netherlands

8. Department of Gynecology, Antoni van Leeuwenhoek, Amsterdam, the Netherlands

9. Department of Gynecologic Oncology, Amsterdam University Medical Center-Center for Gynecological Oncology Amsterdam, Amsterdam, the Netherlands

10. Department of Gynecology, Maastricht University Medical Center, Maastricht, the Netherlands

11. Department of Gynecologic Oncology, University Medical Center Utrecht, Utrecht, the Netherlands

12. Department of Clinical Genetics, University Medical Center Maastricht, Maastricht, the Netherlands

13. Division Laboratories, Pharmacy and Biomedical Genetics, Department of Genetics, University Medical Center Utrecht, Utrecht, the Netherlands

14. Department of Medical Oncology, Erasmus MC Cancer Institute, University Medical Center Rotterdam, Rotterdam, the Netherlands

15. Department of Human Genetics, Amsterdam University Medical Center, Vrije Universiteit Amsterdam, Amsterdam, the Netherlands

16. Department of Clinical Genetics, Leiden University Medical Center, Leiden, the Netherlands

17. Division of Molecular Pathology, Netherlands Cancer Institute, Amsterdam, the Netherlands

18. Department of Clinical Genetics, Radboud University Medical Center, Nijmegen, the Netherlands

19. Hereditary Breast and Ovarian Cancer Research Group Netherlands (HEBON), Coordinating Center: Netherlands Cancer Institute, Amsterdam, the Netherlands

Abstract

PURPOSE To investigate the prevalence of and clinical factors associated with high-grade serous carcinoma (HGSC) at risk-reducing salpingo-oophorectomy (RRSO) in asymptomatic BRCA1/2-pathogenic variant (PV) carriers. PATIENTS AND METHODS We included BRCA1/2-PV carriers who underwent RRSO between 1995 and 2018 from the Hereditary Breast and Ovarian cancer in the Netherlands study. All pathology reports were screened, and histopathology reviews were performed for RRSO specimens with epithelial abnormalities or where HGSC developed after normal RRSO. We then compared clinical characteristics, including parity and oral contraceptive pill (OCP) use, for women with and without HGSC at RRSO. RESULTS Of the 2,557 included women, 1,624 had BRCA1, 930 had BRCA2, and three had both BRCA1/2-PV. The median age at RRSO was 43.0 years (range: 25.3-73.8) for BRCA1-PV and 46.8 years (27.6-77.9) for BRCA2-PV carriers. Histopathologic review confirmed 28 of 29 HGSCs and two further HGSCs from among 20 apparently normal RRSO specimens. Thus, 24 (1.5%) BRCA1-PV and 6 (0.6%) BRCA2-PV carriers had HGSC at RRSO, with the fallopian tube identified as the primary site in 73%. The prevalence of HGSC in women who underwent RRSO at the recommended age was 0.4%. Among BRCA1/2-PV carriers, older age at RRSO increased the risk of HGSC and long-term OCP use was protective. CONCLUSION We detected HGSC in 1.5% ( BRCA1-PV) and 0.6% ( BRCA2-PV) of RRSO specimens from asymptomatic BRCA1/2-PV carriers. Consistent with the fallopian tube hypothesis, we found most lesions in the fallopian tube. Our results highlight the importance of timely RRSO with total removal and assessment of the fallopian tubes and show the protective effects of long-term OCP.

Publisher

American Society of Clinical Oncology (ASCO)

Subject

Cancer Research,Oncology

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