Literature DB >> 33409458

Prevalence of Germline Pathogenic and Likely Pathogenic Variants in Patients With Second Breast Cancers.

Katharine A Yao K1, Jacob Clifford2, Shuwei Li2, Holly LaDuca2, Peter Hulick3, Stephanie Gutierrez2, Mary Helen Black2.   

Abstract

BACKGROUND: Few studies have examined gene-specific associations with contralateral and/or second breast cancer (SBC).
METHODS: The frequency of pathogenic and likely pathogenic (P/LP) variants in clinically actionable genes (BRCA1, BRCA2, PTEN, TP53, CHEK2, CDH1, ATM, PALB2, NBN, and NF1) was compared between women with a primary breast cancer (PBC) and SBC who underwent multigene panel testing at a single diagnostic testing laboratory. Race- and ethnicity-specific logistic regression burden tests adjusted for age at diagnosis of first breast cancer, histology, presence of first- or second-degree relatives with breast cancer, and prior testing for BRCA1/2 genes were used to test for associations with SBC. All statistical tests were 2-sided.
RESULTS: The study was comprised of 75 550 women with PBC and 7728 with SBC. Median time between breast cancers for SBC was 11 (interquartile range = 6-17) years. Restricting to women tested for all actionable genes (n = 60 310), there were 4231 (7.8%) carriers of P/LP variants in actionable genes among the controls (PBC) compared with 652 (11.1%) women with SBC (P< .001). Among Caucasians, exclusive of Ashkenazi Jewish women, those carrying a P/LP variant in a clinically actionable gene were 1.44 (95% confidence interval [CI] = 1.30 to 1.60) times as likely to have SBC than noncarriers, after accounting for potential confounders. Among African American and Hispanic women, a P/LP variant in a clinically actionable gene was 1.88 (95% CI = 1.36 to 2.56) and 1.66 (9% CI = 1.02 to 2.58) times as likely to be associated with SBC, respectively (P < .001 and P = .03).
CONCLUSION: Women with P/LP variants in breast cancer predisposition genes are more likely to have SBC than noncarriers. Prospective studies are needed confirm these findings.
© The Author(s) 2020. Published by Oxford University Press.

Entities:  

Year:  2020        PMID: 33409458      PMCID: PMC7771422          DOI: 10.1093/jncics/pkaa094

Source DB:  PubMed          Journal:  JNCI Cancer Spectr        ISSN: 2515-5091


  38 in total

1.  Social and Clinical Determinants of Contralateral Prophylactic Mastectomy.

Authors:  Sarah T Hawley; Reshma Jagsi; Monica Morrow; Nancy K Janz; Ann Hamilton; John J Graff; Steven J Katz
Journal:  JAMA Surg       Date:  2014-06       Impact factor: 14.766

Review 2.  ATM, radiation, and the risk of second primary breast cancer.

Authors:  Jonine L Bernstein; Patrick Concannon
Journal:  Int J Radiat Biol       Date:  2017-07-27       Impact factor: 2.694

3.  Risk of a second breast cancer associated with hormone-receptor and HER2/neu status of the first breast cancer.

Authors:  Leona Bessonova; Thomas H Taylor; Rita S Mehta; Jason A Zell; Hoda Anton-Culver
Journal:  Cancer Epidemiol Biomarkers Prev       Date:  2011-01-07       Impact factor: 4.254

4.  Radiation exposure, the ATM Gene, and contralateral breast cancer in the women's environmental cancer and radiation epidemiology study.

Authors:  Jonine L Bernstein; Robert W Haile; Marilyn Stovall; John D Boice; Roy E Shore; Bryan Langholz; Duncan C Thomas; Leslie Bernstein; Charles F Lynch; Jorgen H Olsen; Kathleen E Malone; Lene Mellemkjaer; Anne-Lise Borresen-Dale; Barry S Rosenstein; Sharon N Teraoka; Anh T Diep; Susan A Smith; Marinela Capanu; Anne S Reiner; Xiaolin Liang; Richard A Gatti; Patrick Concannon
Journal:  J Natl Cancer Inst       Date:  2010-03-19       Impact factor: 13.506

5.  Increasing rates of contralateral prophylactic mastectomy among patients with ductal carcinoma in situ.

Authors:  Todd M Tuttle; Stephanie Jarosek; Elizabeth B Habermann; Amanda Arrington; Anasooya Abraham; Todd J Morris; Beth A Virnig
Journal:  J Clin Oncol       Date:  2009-02-17       Impact factor: 44.544

6.  Impact that Timing of Genetic Mutation Diagnosis has on Surgical Decision Making and Outcome for BRCA1/BRCA2 Mutation Carriers with Breast Cancer.

Authors:  Akiko Chiba; Tanya L Hoskin; Emily J Hallberg; Jodie A Cogswell; Courtney N Heins; Fergus J Couch; Judy C Boughey
Journal:  Ann Surg Oncol       Date:  2016-06-23       Impact factor: 5.344

7.  Clinical evaluation of a multiple-gene sequencing panel for hereditary cancer risk assessment.

Authors:  Allison W Kurian; Emily E Hare; Meredith A Mills; Kerry E Kingham; Lisa McPherson; Alice S Whittemore; Valerie McGuire; Uri Ladabaum; Yuya Kobayashi; Stephen E Lincoln; Michele Cargill; James M Ford
Journal:  J Clin Oncol       Date:  2014-04-14       Impact factor: 44.544

8.  Gene-panel sequencing and the prediction of breast-cancer risk.

Authors:  Douglas F Easton; Paul D P Pharoah; Antonis C Antoniou; Marc Tischkowitz; Sean V Tavtigian; Katherine L Nathanson; Peter Devilee; Alfons Meindl; Fergus J Couch; Melissa Southey; David E Goldgar; D Gareth R Evans; Georgia Chenevix-Trench; Nazneen Rahman; Mark Robson; Susan M Domchek; William D Foulkes
Journal:  N Engl J Med       Date:  2015-05-27       Impact factor: 91.245

9.  Standards and guidelines for the interpretation of sequence variants: a joint consensus recommendation of the American College of Medical Genetics and Genomics and the Association for Molecular Pathology.

Authors:  Sue Richards; Nazneen Aziz; Sherri Bale; David Bick; Soma Das; Julie Gastier-Foster; Wayne W Grody; Madhuri Hegde; Elaine Lyon; Elaine Spector; Karl Voelkerding; Heidi L Rehm
Journal:  Genet Med       Date:  2015-03-05       Impact factor: 8.822

10.  CHEK2*1100delC heterozygosity in women with breast cancer associated with early death, breast cancer-specific death, and increased risk of a second breast cancer.

Authors:  Maren Weischer; Børge G Nordestgaard; Paul Pharoah; Manjeet K Bolla; Heli Nevanlinna; Laura J Van't Veer; Montserrat Garcia-Closas; John L Hopper; Per Hall; Irene L Andrulis; Peter Devilee; Peter A Fasching; Hoda Anton-Culver; Diether Lambrechts; Maartje Hooning; Angela Cox; Graham G Giles; Barbara Burwinkel; Annika Lindblom; Fergus J Couch; Arto Mannermaa; Grethe Grenaker Alnæs; Esther M John; Thilo Dörk; Henrik Flyger; Alison M Dunning; Qin Wang; Taru A Muranen; Richard van Hien; Jonine Figueroa; Melissa C Southey; Kamila Czene; Julia A Knight; Rob A E M Tollenaar; Matthias W Beckmann; Argyrios Ziogas; Marie-Rose Christiaens; Johanna Margriet Collée; Malcolm W R Reed; Gianluca Severi; Frederik Marme; Sara Margolin; Janet E Olson; Veli-Matti Kosma; Vessela N Kristensen; Alexander Miron; Natalia Bogdanova; Mitul Shah; Carl Blomqvist; Annegien Broeks; Mark Sherman; Kelly-Anne Phillips; Jingmei Li; Jianjun Liu; Gord Glendon; Caroline Seynaeve; Arif B Ekici; Karin Leunen; Mieke Kriege; Simon S Cross; Laura Baglietto; Christof Sohn; Xianshu Wang; Vesa Kataja; Anne-Lise Børresen-Dale; Andreas Meyer; Douglas F Easton; Marjanka K Schmidt; Stig E Bojesen
Journal:  J Clin Oncol       Date:  2012-10-29       Impact factor: 44.544

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  3 in total

1.  Genetic Risk of Second Primary Cancer in Breast Cancer Survivors: The Multiethnic Cohort Study.

Authors:  Fei Chen; Sungshim L Park; Lynne R Wilkens; Peggy Wan; Steven N Hart; Chunling Hu; Siddhartha Yadav; Fergus J Couch; David V Conti; Adam J de Smith; Christopher A Haiman
Journal:  Cancer Res       Date:  2022-09-16       Impact factor: 13.312

2.  Real-world clinical outcomes of patients with BRCA-mutated, human epidermal growth factor receptor 2 (HER2)-negative metastatic breast cancer: a CancerLinQ® study.

Authors:  Robert S Miller; Stella Mokiou; Aliki Taylor; Ping Sun; Katherine Baria
Journal:  Breast Cancer Res Treat       Date:  2022-02-22       Impact factor: 4.872

3.  Eligibility, uptake and response to germline genetic testing in women with DCIS.

Authors:  Lauren Turza; Leann A Lovejoy; Clesson E Turner; Craig D Shriver; Rachel E Ellsworth
Journal:  Front Oncol       Date:  2022-08-26       Impact factor: 5.738

  3 in total

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