Breast cancer risk after age 60 among BRCA1 and BRCA2 mutation carriers


Por: Stjepanovic, N, Lubinski, J, Moller, P, Armel, SR, Foulkes, WD, Tung, N, Neuhausen, SL, Kotsopoulos, J, Sun, P, Sun, S, Eisen, A, Narod, SA, Cajal, T.R., Bordeleau, Louise J.

Publicada: 1 jun 2021 Ahead of Print: 1 ene 2021
Resumen:
Purpose It is not known whether the risk of breast cancer among BRCA1 and BRCA2 mutation carriers after age 60 is high enough to justify intensive screening or prophylactic surgery. Thus, we conducted a prospective analysis of breast cancer risk in BRCA1 and BRCA2 mutation carriers from age 60 until age 80. Methods Subjects had no history of cancer and both breasts intact at age 60 (n = 699). Women were followed until a breast cancer diagnosis, prophylactic bilateral mastectomy or death. We calculated the annual cancer rate and cumulative incidence of breast cancer (invasive and in situ) from age 60 to age 80. We assessed the associations between hormone replacement therapy, family history of breast cancer and bilateral oophorectomy and breast cancer risk. Results Over a mean follow-up of 7.9 years, 61 invasive and 20 in situ breast cancers were diagnosed in the cohort. The mean annual rate of invasive breast cancer was 1.8% for BRCA1 mutation carriers and 1.7% for BRCA2 mutation carriers. The cumulative risk of invasive breast cancer from age 60 to 80 was 20.1% for women with a BRCA1 mutation and was 17.3% for women with a BRCA2 mutation. Hormone replacement therapy, family history and oophorectomy were not associated with breast cancer risk. Conclusions Findings from this large prospective study indicate that the risk of developing breast cancer remains high after age 60 in both BRCA1 and BRCA2 mutation carriers. These findings warrant further evaluation of the role of breast cancer screening in older mutation carriers.

Filiaciones:
Stjepanovic, N:
 Toronto Sunnybrook Reg Canc Ctr, Toronto, ON, Canada

Lubinski, J:
 Pomeranian Med Univ, Int Hereditary Canc Ctr, Dept Genet & Pathol, Szczecin, Poland

Moller, P:
 Oslo Univ Hosp, Norwegian Radium Hosp, Inst Canc Res, Dept Tumor Biol, Oslo, Norway

Armel, SR:
 Univ Hlth Network, Toronto, ON, Canada

Foulkes, WD:
 McGill Univ, Dept Oncol & Human Genet, Program Canc Genet, Montreal, PQ, Canada

Tung, N:
 Beth Israel Deaconess Med Ctr, Boston, MA 02215 USA

Neuhausen, SL:
 City Of Hope, Dept Populat Sci, Div Biomarkers Early Detect & Prevent, Duarte, CA USA

Kotsopoulos, J:
 Womens Coll Hosp, Womens Coll Res Inst, 76 Grenville St,6th Floor, Toronto, ON M5S 1B2, Canada

 Univ Toronto, Dalla Lana Sch Publ Hlth, Toronto, ON, Canada

Sun, P:
 Womens Coll Hosp, Womens Coll Res Inst, 76 Grenville St,6th Floor, Toronto, ON M5S 1B2, Canada

Sun, S:
 BC Canc Agcy, Vancouver, BC, Canada

Eisen, A:
 Toronto Sunnybrook Reg Canc Ctr, Toronto, ON, Canada

Narod, SA:
 Womens Coll Hosp, Womens Coll Res Inst, 76 Grenville St,6th Floor, Toronto, ON M5S 1B2, Canada

 Univ Toronto, Dalla Lana Sch Publ Hlth, Toronto, ON, Canada

Cajal, T.R.:
 Hospital de la Santa Creu i Sant Pau, Barcelona, Spain

Bordeleau, Louise J.:
 McMaster University, Hamilton, Canada
ISSN: 01676806





BREAST CANCER RESEARCH AND TREATMENT
Editorial
SPRINGER, ONE NEW YORK PLAZA, SUITE 4600, NEW YORK, NY, UNITED STATES, Estados Unidos America
Tipo de documento: Article
Volumen: 187 Número: 2
Páginas: 515-523
WOS Id: 000606739300002
ID de PubMed: 33423179

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