TY - JOUR
T1 - A comparison of bilateral breast cancers in BRCA carriers
AU - Weitzel, Jeffrey N.
AU - Robson, Mark
AU - Pasini, Barbara
AU - Manoukian, Siranoush
AU - Stoppa-Lyonnet, Dominique
AU - Lynch, Henry T.
AU - McLennan, Jane
AU - Foulkes, William D.
AU - Wagner, Teresa
AU - Tung, Nadine
AU - Ghadirian, Parviz
AU - Olopade, Olufunmilayo
AU - Isaacs, Claudine
AU - Kim-Sing, Charmaine
AU - Møller, Pal
AU - Neuhausen, Susan L.
AU - Metcalfe, Kelly
AU - Sun, Ping
AU - Narod, Steven A.
PY - 2005/6
Y1 - 2005/6
N2 - Background: Women with breast cancer and a BRCA mutation have a high risk of developing a contralateral breast cancer. It is generally believed that the two cancers represent independent events. However, the extent of concordance between the first and second tumors with respect to hormone receptor expression and other pathologic features is unknown. Purpose: To determine the degree of concordance of estrogen receptor (ER) status, tumor grade, and histology in tumors from women with bilateral breast cancer and a BRCA mutation. Subjects and Methods: Women with a history of bilateral invasive breast cancers were selected from an international registry of women with BRCA1 or BRCA2 mutations. Medical records were reviewed to document the characteristics of each cancer and the treatments received. Results: Data were available for 286 women with bilateral breast cancer and a BRCA mutation (211 BRCA1; 75 BRCA2). The mean interval between first and second tumor was 5.1 years. The two tumors were concordant more often than expected for ER status (P <0.0001) and for grade (P <0.0001), but not for histology (P = 0.55). The ER status of the first tumor was highly predictive of the ER status of the second tumor (odds ratio, 8.7; 95% confidence interval, 3.5-21.5; P <0.0001). Neither age, menopausal status, oophorectomy nor tamoxif en use was predictive of the ER status of the second tumor. Conclusions: There is strong concordance in ER status and tumor grade between independent primary breast tumors in women with a BRCA mutation. The excess concordance may be due to common risk factors, genetic variation, or the existence of a preneoplastic lesion that is common to both tumors.
AB - Background: Women with breast cancer and a BRCA mutation have a high risk of developing a contralateral breast cancer. It is generally believed that the two cancers represent independent events. However, the extent of concordance between the first and second tumors with respect to hormone receptor expression and other pathologic features is unknown. Purpose: To determine the degree of concordance of estrogen receptor (ER) status, tumor grade, and histology in tumors from women with bilateral breast cancer and a BRCA mutation. Subjects and Methods: Women with a history of bilateral invasive breast cancers were selected from an international registry of women with BRCA1 or BRCA2 mutations. Medical records were reviewed to document the characteristics of each cancer and the treatments received. Results: Data were available for 286 women with bilateral breast cancer and a BRCA mutation (211 BRCA1; 75 BRCA2). The mean interval between first and second tumor was 5.1 years. The two tumors were concordant more often than expected for ER status (P <0.0001) and for grade (P <0.0001), but not for histology (P = 0.55). The ER status of the first tumor was highly predictive of the ER status of the second tumor (odds ratio, 8.7; 95% confidence interval, 3.5-21.5; P <0.0001). Neither age, menopausal status, oophorectomy nor tamoxif en use was predictive of the ER status of the second tumor. Conclusions: There is strong concordance in ER status and tumor grade between independent primary breast tumors in women with a BRCA mutation. The excess concordance may be due to common risk factors, genetic variation, or the existence of a preneoplastic lesion that is common to both tumors.
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U2 - 10.1158/1055-9965.EPI-05-0070
DO - 10.1158/1055-9965.EPI-05-0070
M3 - Article
C2 - 15941968
AN - SCOPUS:20444387248
SN - 1055-9965
VL - 14
SP - 1534
EP - 1538
JO - Cancer Epidemiology Biomarkers and Prevention
JF - Cancer Epidemiology Biomarkers and Prevention
IS - 6
ER -