Literature DB >> 20135344

Adjuvant systemic therapy for breast cancer in BRCA1/BRCA2 mutation carriers in a population-based study of risk of contralateral breast cancer.

Kerryn W Reding1, Jonine L Bernstein, Bryan M Langholz, Leslie Bernstein, Robert W Haile, Colin B Begg, Charles F Lynch, Patrick Concannon, Ake Borg, Sharon N Teraoka, Therese Törngren, Anh Diep, Shanyan Xue, Lisbeth Bertelsen, Xiaolin Liang, Anne S Reiner, Marinela Capanu, Kathleen E Malone.   

Abstract

Given the greatly elevated risks of contralateral breast cancer (CBC) observed in breast cancer patients who carry mutations in BRCA1 and BRCA2, it is critical to determine the effectiveness of standard adjuvant therapies in preventing CBC in mutation carriers. The WECARE study is a matched, case-control study of 708 women with CBC as cases and 1,399 women with unilateral breast cancer (UBC) as controls, including 181 BRCA1/BRCA2 mutation carriers. Interviews and medical record reviews provided detailed information on risk factors and breast cancer therapy. All study participants were screened for BRCA1 and BRCA2 mutations using denaturing high-performance liquid chromatography (DHPLC) to detect genetic variants in the coding and flanking regions of the genes. Conditional logistic regression was used to compare the risk of CBC associated with chemotherapy and tamoxifen in BRCA1/BRCA2 mutation carriers and non-carriers. Chemotherapy was associated with lower CBC risk both in non-carriers (RR = 0.6 [95% CI: 0.5-0.7]) and carriers (RR = 0.5 [95% CI: 0.2-1.0]; P value = 0.04). Tamoxifen was associated with a reduced CBC risk in non-carriers (RR = 0.7 [95% CI: 0.6-1.0]; P value = 0.03). We observed a similar but non-significant reduction associated with tamoxifen in mutation carriers (RR = 0.7 [95% CI: 0.3-1.8]). The tests of heterogeneity comparing carriers to non-carriers did not provide evidence for a difference in the associations with chemotherapy (P value = 0.51) nor with tamoxifen (P value = 0.15). Overall, we did not observe a difference in the relative risk reduction associated with adjuvant treatment between BRCA1/BRCA2 mutation carriers and non-carriers. However, given the higher absolute CBC risk in mutation carriers, the potentially greater impact of adjuvant therapy in reducing CBC risk among mutation carriers should be considered when developing treatment plans for these patients.

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Year:  2010        PMID: 20135344      PMCID: PMC2903659          DOI: 10.1007/s10549-010-0769-3

Source DB:  PubMed          Journal:  Breast Cancer Res Treat        ISSN: 0167-6806            Impact factor:   4.872


  30 in total

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Authors:  Rachel Nusbaum; Claudine Isaacs
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9.  Study design: evaluating gene-environment interactions in the etiology of breast cancer - the WECARE study.

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Authors:  Richard D Kennedy; Jennifer E Quinn; Paul B Mullan; Patrick G Johnston; D Paul Harkin
Journal:  J Natl Cancer Inst       Date:  2004-11-17       Impact factor: 13.506

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  20 in total

1.  Second primary breast cancer in BRCA1 and BRCA2 mutation carriers: 10-year cumulative incidence in the Breast Cancer Family Registry.

Authors:  Tehillah S Menes; Mary Beth Terry; David Goldgar; Irene L Andrulis; Julia A Knight; Esther M John; Yuyan Liao; Melissa Southey; Alexander Miron; Wendy Chung; Saundra S Buys
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Review 2.  Focus on the glycerophosphocholine pathway in choline phospholipid metabolism of cancer.

Authors:  Kanchan Sonkar; Vinay Ayyappan; Caitlin M Tressler; Oluwatobi Adelaja; Ruoqing Cai; Menglin Cheng; Kristine Glunde
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Journal:  Cancer J       Date:  2011 Nov-Dec       Impact factor: 3.360

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Journal:  Fam Cancer       Date:  2011-09       Impact factor: 2.375

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Authors:  Leila Green; Funda Meric-Bernstam
Journal:  Curr Breast Cancer Rep       Date:  2011-09-01

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Journal:  Cancer Prev Res (Phila)       Date:  2014-05-09

Review 7.  Bilateral breast cancers.

Authors:  Steven A Narod
Journal:  Nat Rev Clin Oncol       Date:  2014-02-04       Impact factor: 66.675

8.  A randomized controlled trial of diet and physical activity in BRCA mutation carriers.

Authors:  P Pasanisi; E Bruno; S Manoukian; F Berrino
Journal:  Fam Cancer       Date:  2014-06       Impact factor: 2.375

9.  Tamoxifen and risk of contralateral breast cancer for BRCA1 and BRCA2 mutation carriers.

Authors:  Kelly-Anne Phillips; Roger L Milne; Matti A Rookus; Mary B Daly; Antonis C Antoniou; Susan Peock; Debra Frost; Douglas F Easton; Steve Ellis; Michael L Friedlander; Saundra S Buys; Nadine Andrieu; Catherine Noguès; Dominique Stoppa-Lyonnet; Valérie Bonadona; Pascal Pujol; Sue Anne McLachlan; Esther M John; Maartje J Hooning; Caroline Seynaeve; Rob A E M Tollenaar; David E Goldgar; Mary Beth Terry; Trinidad Caldes; Prue C Weideman; Irene L Andrulis; Christian F Singer; Kate Birch; Jacques Simard; Melissa C Southey; Håkan L Olsson; Anna Jakubowska; Edith Olah; Anne-Marie Gerdes; Lenka Foretova; John L Hopper
Journal:  J Clin Oncol       Date:  2013-08-05       Impact factor: 44.544

10.  Common variants in genes coding for chemotherapy metabolizing enzymes, transporters, and targets: a case-control study of contralateral breast cancer risk in the WECARE Study.

Authors:  Jennifer D Brooks; Sharon N Teraoka; Leslie Bernstein; Lene Mellemkjær; Kathleen E Malone; Charles F Lynch; Robert W Haile; Patrick Concannon; Anne S Reiner; David J Duggan; Katherine Schiermeyer; Jonine L Bernstein; Jane C Figueiredo
Journal:  Cancer Causes Control       Date:  2013-06-18       Impact factor: 2.506

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