Endometrial Cancer Risk Among Germline BRCA1/2 Pathogenic Variant Carriers: Review of Our Current Understanding and Next Steps

Author:

Sorouri Kimia12ORCID,Lynce Filipa123ORCID,Feltmate Colleen M.124,Davis Michelle R.124,Muto Michael G.124,Konstantinopoulos Panagiotis A.125ORCID,Stover Elizabeth H.125ORCID,Kurian Allison W.6ORCID,Hill Sarah J.12ORCID,Partridge Ann H.123ORCID,Tolaney Sara M.123ORCID,Garber Judy E.1237ORCID,Bychkovsky Brittany L.1237ORCID

Affiliation:

1. Medical Oncology, Dana-Farber Cancer Institute, Boston, MA

2. Harvard Medical School, Boston, MA

3. Breast Oncology Program, Dana-Farber Brigham Cancer Center, Boston, MA

4. Department of Obstetrics and Gynecology, Division of Gynecologic Oncology, Brigham and Women's Hospital, Boston, MA

5. Division of Gynecologic Oncology, Dana-Farber Cancer Institute, Boston, MA

6. Stanford University School of Medicine, Stanford, CA

7. Division of Cancer Genetics and Prevention, Dana-Farber Cancer Institute, Boston, MA

Abstract

PURPOSE To review the literature exploring endometrial cancer (EC) risk among surgical candidates with germline BRCA1/2 pathogenic variants (PVs) to guide decisions around risk-reducing (rr) hysterectomy in this population. DESIGN A comprehensive review was conducted of the current literature that influences clinical practice and informs expert consensus. We present our understanding of EC risk among BRCA1/2 PV carriers, the risk-modifying factors specific to this patient population, and the available research technology that may guide clinical practice in the future. Limitations of the existing literature are outlined. RESULTS Patients with BRCA1/2 PVs, those with a personal history of tamoxifen use, those who desire long-term hormone replacement therapy, and/or have an elevated BMI are at higher risk of EC, primarily endometrioid EC and/or uterine papillary serous carcinoma, and may benefit from rr-hysterectomy. Although prescriptive clinical guidelines specific to BRCA1/2 PV carriers could inform decisions around rr-hysterectomy, limitations of the current literature prevent more definitive guidance at this time. A large population-based study of a contemporary cohort of BRCA1/2 PV carriers with lifetime follow-up compared with cancer-gene negative controls would advance this topic and facilitate care decisions. CONCLUSION This review validates a potential role for rr-hysterectomy to address EC risk among surgical candidates with BRCA1/2 PVs. Evidence-based clinical guidelines for rr-hysterectomy in BRCA1/2 PV carriers are essential to ensure equitable access to this preventive measure, supporting insurance coverage for patients with either BRCA1 or BRCA2 PVs to pursue rr-hysterectomy. Overall, this review highlights the complexity of EC risk in BRCA1/2 PV carriers and offers a comprehensive framework to shared decision making to inform rr-hysterectomy for BRCA1/2 PV carriers.

Publisher

American Society of Clinical Oncology (ASCO)

Subject

Cancer Research,Oncology

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