Survival from breast cancer in women with a BRCA2 mutation by treatment

D Gareth Evans1, Kelly-Anne Phillips2,3,4, Roger L Milne4,5,6

  • 1Genomic Medicine, Manchester Academic Health Science Centre, The University of Manchester, Manchester, UK.

British Journal of Cancer
|February 18, 2021
PubMed
Abstract

Insights

Bilateral oophorectomy significantly improves breast cancer survival for women with a BRCA2 mutation. This treatment, unlike ER status, is a key factor in reducing breast cancer mortality in this population.

Area of Science:

  • Oncology
  • Genetics
  • Surgical Oncology

Background:

  • Limited research exists on breast cancer treatment outcomes for BRCA2 mutation carriers.
  • Understanding treatment impact is crucial for personalized medicine in hereditary breast cancer.

Purpose of the Study:

  • To evaluate the effect of bilateral oophorectomy and other treatments on breast cancer-specific survival.
  • To identify prognostic factors for survival in patients with germline BRCA2 mutations.

Main Methods:

  • Retrospective and prospective data from 664 women with stage I-III breast cancer and BRCA2 mutations were combined.
  • Survival analysis was performed using Cox proportional hazard models, adjusting for prognostic features and treatments.
  • Patient-reported and medical record data were used for tumor characteristics and treatment information.

Main Results:

  • Bilateral oophorectomy was associated with a significant reduction in breast cancer mortality (adjusted HR=0.45; p=0.001).
  • Estrogen receptor (ER) status did not significantly predict breast cancer survival (adjusted HR=1.23; p=0.55).
  • Chemotherapy showed a non-significant trend towards improved survival (adjusted HR=0.83; p=0.56).

Conclusions:

  • Oophorectomy is a critical intervention for improving survival in BRCA2-mutated breast cancer patients.
  • ER status is not a reliable predictor of survival in this cohort.
  • Oophorectomy should be strongly considered in the management of breast cancer in women with BRCA2 mutations.

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