Survival Outcomes With or Without Risk-Reducing Mastectomy in <i>BRCA1</i> and <i>BRCA2</i> Pathogenic Variant Carriers
Abstract
PURPOSE Many women carrying pathogenic variants (pvs) of BRCA1 and BRCA2 genes (pv BRCA 1/2 ) elect to undergo bilateral risk-reducing mastectomy (BRRM) in the belief that it will improve their overall survival (OS). Although many are satisfied with their decision to undergo BRRM a significant minority exhibit regret. We compared long-term oncology outcomes in women with pv BRCA1/2 choosing BRRM with those choosing a program of imaging surveillance. METHODS All participants were attendees at a regional family history/genetics service and had undergone genetic testing for pv BRCA 1/2 . Carriers of pv BRCA1/2 elected either to undergo BRRM or imaging surveillance as directed by UK national guidance. A prospective cohort design examined OS, breast cancer–specific death, and breast cancer incidence between the study groups. RESULTS A total of 460 women elected to undergo BRRM, while 745 chose surveillance (median age, 37.2 years and 38.5 years, respectively; P = .06). Follow-up totaled 4,652 woman-years after BRRM. Overall annual incidence rate of breast cancer was 2.4%, falling to 0.15% after BRRM, a 94% reduction compared with surveillance alone (log-rank chi-square = 86.1; P < .001). There were nine occult cancers diagnosed at BRRM (2%). Breast cancer–specific deaths were similar in the BRRM and surveillance groups (two and four deaths, respectively; P = .36; 4,634 and 5,419 woman-years of follow-up, respectively). Proportionately, deaths from breast cancer were similar to deaths from ovarian cancer in both treatment groups. CONCLUSION For women electing imaging surveillance over risk-reducing surgery, our results may offer reassurance that their breast cancer–specific survival and OS are unlikely to be compromised. However, breast cancer incidence rates are significantly reduced after BRRM compared with imaging surveillance, which may be important information for women with pv BRCA 1/2 considering BRRM.
Article Details
Journal Info
Journal of Clinical Oncology
Lippincott Williams & Wilkins
Authors (10)
Ashu Gandhi
Ashu Gandhi, MD, Division of Cancer Sciences, Faculty of Biology, Medicine & Health, University of Manchester, Manchester, United Kingdom, Manchester University Hospitals, Manchester, United Kingdom, Manchester Academic Health Sciences Centre & Manchester Breast Centre, University of Manchester, Manchester, United Kingdom; Sacha J. Howell, PhD, Division of Cancer Sciences, Faculty of Biology, Medicine & Health, University of Manchester, Manchester, United Kingdom, Manchester University Hospitals, Manchester, United Kingdom, Manchester Academic Health Sciences Centre & Manchester Breast Centre, University of Manchester, Manchester, United Kingdom, Christie Hospital NHS Foundation Trust, Manchester, United Kingdom; and D. Gareth Evans, MD, Manchester University Hospitals, Manchester, United Kingdom, Manchester Academic Health Sciences Centre & Manchester Breast Centre, University of Manchester, Manchester, United Kingdom, Manchester Centre for Genomic Medicine, Manchester University Hospi...
Sacha J. Howell
Elaine F. Harkness
Emma Woodward
Manchester Centre for Genomic Medicine, Manchester University Hospitals NHS Foundation Trust, Manchester, United Kingdom
Fiona Lalloo
Claire Forde
Manchester Centre for Genomic Medicine, Manchester University Hospitals NHS Foundation Trust, Manchester, United Kingdom
James Harvey
The Nightingale and PREVENT Breast Cancer Centre, Manchester University NHS Foundation Trust & Faculty of Biology, Medicine and Health, University of Manchester, Manchester, United Kingdom
Lyndsey Highton
Manchester University Hospitals, Manchester, United Kingdom
Nicola Flaum
Division of Cancer Sciences, Faculty of Biology, Medicine & Health, University of Manchester, Manchester, United Kingdom
D. Gareth Evans