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Risks of Breast, Ovarian, and Contralateral Breast Cancer for BRCA1 and BRCA2 Mutation Carriers

Publikation: Bidrag til tidsskriftTidsskriftartikelForskningpeer review


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  • Karoline B Kuchenbaecker
  • John L Hopper
  • Daniel R Barnes
  • Kelly-Anne Phillips
  • Thea M Mooij
  • Marie-José Roos-Blom
  • Sarah Jervis
  • Flora E van Leeuwen
  • Roger L Milne
  • Nadine Andrieu
  • David E Goldgar
  • Mary Beth Terry
  • Matti A Rookus
  • Douglas F Easton
  • Antonis C Antoniou
  • BRCA1 and BRCA2 Cohort Consortium
  • Lesley McGuffog
  • D Gareth Evans
  • Daniel Barrowdale
  • Debra Frost
  • Julian Adlard
  • Kai-Ren Ong
  • Louise Izatt
  • Marc Tischkowitz
  • Ros Eeles
  • Rosemarie Davidson
  • Shirley Hodgson
  • Steve Ellis
  • Catherine Nogues
  • Christine Lasset
  • Dominique Stoppa-Lyonnet
  • Jean-Pierre Fricker
  • Laurence Faivre
  • Pascaline Berthet
  • Maartje J Hooning
  • Lizet E van der Kolk
  • Carolien M Kets
  • Muriel A Adank
  • Esther M John
  • Wendy K Chung
  • Irene L Andrulis
  • Melissa Southey
  • Mary B Daly
  • Saundra S Buys
  • Ana Osorio
  • Christoph Engel
  • Karin Kast
  • Rita K Schmutzler
  • Trinidad Caldes
  • Anna Jakubowska
  • Jacques Simard
  • Michael L Friedlander
  • Sue-Anne McLachlan
  • Eva Machackova
  • Lenka Foretova
  • Yen Y Tan
  • Christian F Singer
  • Edith Olah
  • Anne-Marie Gerdes
  • Brita Arver
  • Håkan Olsson
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Importance: The clinical management of BRCA1 and BRCA2 mutation carriers requires accurate, prospective cancer risk estimates.

Objectives: To estimate age-specific risks of breast, ovarian, and contralateral breast cancer for mutation carriers and to evaluate risk modification by family cancer history and mutation location.

Design, Setting, and Participants: Prospective cohort study of 6036 BRCA1 and 3820 BRCA2 female carriers (5046 unaffected and 4810 with breast or ovarian cancer or both at baseline) recruited in 1997-2011 through the International BRCA1/2 Carrier Cohort Study, the Breast Cancer Family Registry and the Kathleen Cuningham Foundation Consortium for Research into Familial Breast Cancer, with ascertainment through family clinics (94%) and population-based studies (6%). The majority were from large national studies in the United Kingdom (EMBRACE), the Netherlands (HEBON), and France (GENEPSO). Follow-up ended December 2013; median follow-up was 5 years.

Exposures: BRCA1/2 mutations, family cancer history, and mutation location.

Main Outcomes and Measures: Annual incidences, standardized incidence ratios, and cumulative risks of breast, ovarian, and contralateral breast cancer.

Results: Among 3886 women (median age, 38 years; interquartile range [IQR], 30-46 years) eligible for the breast cancer analysis, 5066 women (median age, 38 years; IQR, 31-47 years) eligible for the ovarian cancer analysis, and 2213 women (median age, 47 years; IQR, 40-55 years) eligible for the contralateral breast cancer analysis, 426 were diagnosed with breast cancer, 109 with ovarian cancer, and 245 with contralateral breast cancer during follow-up. The cumulative breast cancer risk to age 80 years was 72% (95% CI, 65%-79%) for BRCA1 and 69% (95% CI, 61%-77%) for BRCA2 carriers. Breast cancer incidences increased rapidly in early adulthood until ages 30 to 40 years for BRCA1 and until ages 40 to 50 years for BRCA2 carriers, then remained at a similar, constant incidence (20-30 per 1000 person-years) until age 80 years. The cumulative ovarian cancer risk to age 80 years was 44% (95% CI, 36%-53%) for BRCA1 and 17% (95% CI, 11%-25%) for BRCA2 carriers. For contralateral breast cancer, the cumulative risk 20 years after breast cancer diagnosis was 40% (95% CI, 35%-45%) for BRCA1 and 26% (95% CI, 20%-33%) for BRCA2 carriers (hazard ratio [HR] for comparing BRCA2 vs BRCA1, 0.62; 95% CI, 0.47-0.82; P=.001 for difference). Breast cancer risk increased with increasing number of first- and second-degree relatives diagnosed as having breast cancer for both BRCA1 (HR for ≥2 vs 0 affected relatives, 1.99; 95% CI, 1.41-2.82; P<.001 for trend) and BRCA2 carriers (HR, 1.91; 95% CI, 1.08-3.37; P=.02 for trend). Breast cancer risk was higher if mutations were located outside vs within the regions bounded by positions c.2282-c.4071 in BRCA1 (HR, 1.46; 95% CI, 1.11-1.93; P=.007) and c.2831-c.6401 in BRCA2 (HR, 1.93; 95% CI, 1.36-2.74; P<.001).

Conclusions and Relevance: These findings provide estimates of cancer risk based on BRCA1 and BRCA2 mutation carrier status using prospective data collection and demonstrate the potential importance of family history and mutation location in risk assessment.

TidsskriftJAMA - Journal of the American Medical Association
Udgave nummer23
Sider (fra-til)2402-2416
Antal sider15
StatusUdgivet - 20 jun. 2017

ID: 52409225