Risk of ipsilateral breast cancer in BRCA1 and BRCA2 mutation carriers

被引:0
作者
Kelly Metcalfe
Henry T. Lynch
Parviz Ghadirian
Nadine Tung
Charmaine Kim-Sing
Olufunmilayo I. Olopade
Susan Domchek
Andrea Eisen
William D. Foulkes
Barry Rosen
Danny Vesprini
Ping Sun
Steven A. Narod
机构
[1] Lawrence S. Bloomberg Faculty of Nursing,Department of Preventive Medicine and Public Health
[2] University of Toronto,Epidemiology Research Unit
[3] Women’s College Research Institute,Department of Medicine
[4] Creighton University School of Medicine,Departments of Medicine and Genetics
[5] Centre Hospitalier de Université de Montreal (CHUM),Department of Hematology/Oncology
[6] Beth Israel Deaconess Medical Center,Program in Cancer Genetics, Departments of Oncology and Human Genetics
[7] BC Cancer Agency,undefined
[8] University of Chicago,undefined
[9] University of Pennsylvania,undefined
[10] University of Pennsylvania,undefined
[11] Sunnybrook Odette Cancer Center,undefined
[12] McGill University,undefined
[13] University Health Network,undefined
来源
Breast Cancer Research and Treatment | 2011年 / 127卷
关键词
Breast Cancer; Tamoxifen; BRCA2 Mutation; Primary Breast Cancer; Contralateral Breast Cancer;
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摘要
Women with a BRCA1 or BRCA2 mutation have an elevated risk of breast cancer and of contralateral breast cancer. In this study, we estimate the risk of non-synchronous ipsilateral breast cancer after a diagnosis of breast cancer in BRCA carriers and evaluate the effects of various treatments on this risk. Patients were 396 women with stage I or stage II breast cancer with an intact ipsilateral breast and for whom a BRCA1 or BRCA2 mutation had been identified in the family. Patients were followed from the initial diagnosis of cancer until the first of ipsilateral mastectomy, ipsilateral breast cancer, death or last follow-up. The 5-year actuarial risk of ipsilateral breast cancer was 5.8% (95% CI 3.2–8.4%) and the 10-year risk was 12.9% (95% CI 8.7–17.1%). Subjects who received chemotherapy had a significantly lower risk of ipsilateral breast cancer compared to those who did not receive chemotherapy (RR 0.45; 95% CI 0.24–0.84; P = 0.01). Radiotherapy was associated with a reduced risk of ipsilateral breast cancer (RR 0.28; 95% CI 0.12–0.63; P = 0.002). Oophorectomy was associated with a significant reduction in the risk of ipsilateral breast cancer (RR 0.33; 95% CI; 0.13–0.81; P = 0.02). On average, following a diagnosis of breast cancer, the annual risk of ipsilateral breast cancer risk in BRCA mutation carriers is 1.2% per year. For women treated with chemotherapy, radiation therapy or oophorectomy the risk is low, compared to women who did not receive any of these treatments.
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页码:287 / 296
页数:9
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