Breast cancer after ovarian cancer in BRCA1 and BRCA2 pathogenic variant heterozygotes: Lower rates for 5 years post chemotherapy

  • 0Manchester Centre for Genomic Medicine, Manchester University Hospitals NHS Foundation Trust, Manchester, United Kingdom; Division of Evolution and Genomic Sciences, School of Biological Sciences, Faculty of Biology, Medicine and Health, University of Manchester, Manchester Academic Health Science Centre, Manchester, United Kingdom; Prevent Breast Cancer Centre, Wythenshawe Hospital Manchester Universities Foundation Trust, Wythenshawe, Manchester, United Kingdom; Manchester Breast Centre, The Christie NHS Foundation Trust, Wilmslow Road, Manchester, United Kingdom.

Summary

This summary is machine-generated.

Women with BRCA1/BRCA2 pathogenic variants (PV) have a low initial breast cancer risk after ovarian cancer diagnosis, likely due to chemotherapy. However, risk increases significantly after 10 years, especially for BRCA1 carriers.

Area Of Science

  • Oncology
  • Genetics
  • Cancer Epidemiology

Background

  • Germline BRCA1/BRCA2 pathogenic variants (PV) are associated with elevated lifetime risks of breast and ovarian cancers.
  • Limited data exists on breast cancer incidence following an ovarian cancer diagnosis in individuals with these variants.

Purpose Of The Study

  • To assess the incidence and patterns of breast cancer in women with germline BRCA1/BRCA2 PV after an ovarian cancer diagnosis.
  • To evaluate the impact of platinum-based chemotherapy on subsequent breast cancer risk.

Main Methods

  • Retrospective review of breast cancer history in 895 women with BRCA1/BRCA2 PV heterozygotes (541 with BRCA1 PV).
  • Calculation of cumulative annual breast cancer incidence at 2, 5, and 10+ years post-ovarian cancer diagnosis.
  • Analysis of breast cancer pathology and mortality in relation to prior ovarian cancer diagnosis.

Main Results

  • Breast cancer incidence was low at 2 years (1.18%) and 2-5 years (1.13%) but rose significantly after 10 years (>4% annually) for BRCA1 PV carriers.
  • BRCA1 PV carriers diagnosed with breast cancer post-ovarian cancer showed less high-grade triple-negative and more lower-grade hormone-receptor-positive disease.
  • Breast cancer accounted for <4% of all deaths in the cohort but was the cause of death in 50% of women who developed breast cancer after ovarian cancer.

Conclusions

  • Breast cancer incidence is initially low after ovarian cancer diagnosis in BRCA1/BRCA2 PV carriers, potentially due to platinum-based chemotherapy.
  • Awareness of increasing breast cancer incidence over time, particularly beyond 10 years, is crucial for these women.
  • While initial risk is reassuring, long-term surveillance for breast cancer is warranted.

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