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Kotsopoulos, Joanne

https://orcid.org/0000-0001-9624-4218

Mayo Clinic

University of Toronto

Citations 12

The risks of cancer in older women with BRCA pathogenic variants: How far have we come?
Metcalfe, Kelly , McCuaig, Jeanna , Eisen, Andrea , Elser, Christine , Senter, Leigha , Møller, Pål , Bordeleau, Louise , Velsher, Lea, Zakalik, Dana , Olopade, Olufunmilayo I. , Cullinane, Carey A., Sun, Ping , Narod, Steven A. , Metcalfe, Kelly A , Olopade, Olufunmilayo I , Kotsopoulos, Joanne , Narod, Steven A , Senter, Leigha , Eisen, Andrea , Bordeleau, Louise , Gronwald, Jacek , Tung, Nadine , Foulkes, William D. , Neuhausen, Susan L. , Fruscio, Robert , Eng, Charis , Pal, Tuya , Couch, Fergus J. , Kotsopoulos, Joanne , Lubiński, Jan

Cancer | December 26, 2022 | Volume: 129 | Issue: 6 | Pages: 901-907

10.1002/cncr.34615 Get It

AbstractBackgroundThe purpose of this study was to estimate the cumulative risks of all cancers in women from 50 to 75 years of age with a BRCA1 or BRCA2 pathogenic variant.MethodsParticipants were women with BRCA1 or BRCA2 pathogenic variants from 85 centers in 16 countries. Women were eligible if they had no cancer before the age of 50 years. Participants completed a baseline questionnaire and follow‐up questionnaires every 2 years. Women were followed from age 50 until a diagnosis of cancer, death, age 75, or last follow‐up. The risk of all cancers combined from age 50 to 75 was estimated using the Kaplan–Meier method.ResultsThere were 2211 women included (1470 BRCA1 and 742 BRCA2). There were 379 cancers diagnosed in the cohort between 50 and 75 years. The actuarial risk of any cancer from age 50 to 75 was 49% for BRCA1 and 43% for BRCA2. Breast (n = 186) and ovarian (n = 45) were the most frequent cancers observed. For women who had both risk‐reducing mastectomy and bilateral salpingo‐oophorectomy before age 50, the risk of developing any cancer between age 50 and 75 was 9%.ConclusionWomen with a BRCA1 or BRCA2 pathogenic variant have a high risk of cancer between the ages of 50 and 75 years and should be counselled appropriately.
Bilateral Oophorectomy and the Risk of Breast Cancer in BRCA1 Mutation Carriers: A Reappraisal
Menkiszak, Janusz , McCuaig, Jeanna , Metcalfe, Kelly , Foulkes, William D. , Sun, Sophie , Karlan, Beth Y. , Eisen, Andrea , Olopade, Olufunmilayo I. , Senter, Leigha , Bordeleau, Louise , Sun, Ping , Narod, Steven A. , Kim, Raymond H. , Menkiszak, Janusz , Foulkes, William D , Karlan, Beth Y , Olopade, Olufunmilayo I , Couch, Fergus J. , Huzarski, Tomasz , Senter, Leigha , Singer, Christian F , Eng, Charis , Fruscio, Robert , Narod, Steven A , Metcalfe, Kelly A , Eisen, Andrea , Bordeleau, Louise , Kim, Raymond H , Kotsopoulos, Joanne , Lubiński, Jan , Gronwald, Jacek , Neuhausen, Susan L. , Tung, Nadine , Couch, Fergus J. , Huzarski, Tomasz , Singer, Christian F. , Eng, Charis , Fruscio, Robert , Pal, Tuya

Cancer Epidemiology, Biomarkers & Prevention | April 27, 2022 | Volume: 31 | Issue: 7 | Pages: 1351-1358

10.1158/1055-9965.epi-21-1196 Get It

Abstract Background: The lack of consensus on whether bilateral oophorectomy impacts risk of developing breast cancer among BRCA1 mutation carriers might be attributed to various biases, specifically, cancer-induced testing bias due to inclusion of prevalent cases. We conducted two complementary matched case–control analyses to evaluate the association of oophorectomy and BRCA1 breast cancer. Methods: A research questionnaire was administered every two years to collect information on exposures and disease. In the first analysis, we limited the study to prevalent breast cancer cases (diagnosed prior to study entry; n = 2,962) who were matched to controls on year of birth and country of residence (n = 4,358). In the second approach, we limited to 330 incident cases (diagnosed in the follow-up period) and 1,548 matched controls. Conditional logistic regression was used to estimate the adjusted odds ratios (OR) and 95% confidence intervals (CI) of invasive breast cancer. Results: In the first approach, there was a significant inverse association between oophorectomy and the risk of developing breast cancer [OR = 0.43; 95% confidence interval (CI), 0.34–0.55; P < 00001]. In the second approach, there was no association between oophorectomy and risk (OR = 1.21; 95% CI, 0.87–1.70; P = 0.26). Conclusions: The inclusion of women with a personal history of breast cancer prior to ascertainment likely impacts upon the association of oophorectomy and BRCA1 breast cancer risk. Impact: Oophorectomy is unlikely a determinant of breast cancer risk in BRCA1 mutation carriers but should be offered at age 35 to reduce the risk of ovarian and fallopian tube cancer.