Literature DB >> 21248744

Breast and ovarian cancer screening of non-carriers from BRCA1/2 mutation-positive families: 2-year follow-up of cohorts from France and Quebec.

Michel Dorval1, Catherine Noguès, Pascaline Berthet, Jocelyne Chiquette, Marion Gauthier-Villars, Christine Lasset, Claude Picard, Marie Plante, Jacques Simard, Claire Julian-Reynier.   

Abstract

We described and compared breast and ovarian screening practices in the 2-year period following test result disclosure in female non-carriers from BRCA1/2 mutation-positive families living in two countries, France and Quebec, Canada, which provide universal health care. Four hundred and two (France n=293; Quebec n=109) unaffected female non-carriers from BRCA-proven mutation families provided information about the uptake of mammography, clinical breast examination, breast self-examination, and ovarian ultrasounds using self-administered questionnaires. The frequency of screening practices between study cohorts were compared using logistic regression. Annual mammography was conducted in 23 and 43% of French and Quebecer women participants <50 years of age, respectively (adjusted odds ratio (aOR)=2.72; 95% confidence interval (CI), 1.08-6.81). In women ≥ 50 years of age, mammography was conducted in 49 and 65% of French and Quebecer participants (aOR=1.77; 95% CI, 0.07-4.51). Overall, 33% of French women and 39% of Quebecer women underwent at least one ovarian ultrasound during the 2-year period following BRCA1/2 test result with no significant difference between cohorts of women < 50 years of age. Among older women, Quebecers reported more frequently than French women that they had undergone ultrasound once (aOR=3.00; 95% CI, 1.02-8.83). The frequency of cancer screening practices for female non-carriers from BRCA1/2 mutation-positive families in both France and Quebec exceeded those recommended for similarly aged women in the general population. Our findings highlight the need for clearcut recommendations on the follow-up of women from BRCA1/2 families who are not themselves carriers of a BRCA1/2 mutation.

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Year:  2011        PMID: 21248744      PMCID: PMC3083614          DOI: 10.1038/ejhg.2010.227

Source DB:  PubMed          Journal:  Eur J Hum Genet        ISSN: 1018-4813            Impact factor:   4.246


  24 in total

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5.  Evaluation of BRCA1 and BRCA2 mutation prevalence, risk prediction models and a multistep testing approach in French-Canadian families with high risk of breast and ovarian cancer.

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Review 9.  Risk assessment and genetic counseling for hereditary breast and ovarian cancer: recommendations of the National Society of Genetic Counselors.

Authors:  Janice L Berliner; Angela Musial Fay
Journal:  J Genet Couns       Date:  2007-05-17       Impact factor: 2.717

10.  Predictive genetic testing for BRCA1/2 in a UK clinical cohort: three-year follow-up.

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  8 in total

1.  Family communication following BRCA1/2 genetic testing: a close look at the process.

Authors:  Darquise Lafrenière; Karine Bouchard; Béatrice Godard; Jacques Simard; Michel Dorval
Journal:  J Genet Couns       Date:  2012-12-16       Impact factor: 2.537

2.  Self-reported mammography use following BRCA1/2 genetic testing may be overestimated.

Authors:  Geneviève Larouche; Karine Bouchard; Jocelyne Chiquette; Christine Desbiens; Jacques Simard; Michel Dorval
Journal:  Fam Cancer       Date:  2012-03       Impact factor: 2.375

3.  Genetic counseling content: How does it impact health behavior?

Authors:  Kimberly M Kelly; Lee Ellington; Nancy Schoenberg; Thomas Jackson; Stephanie Dickinson; Kyle Porter; Howard Leventhal; Michael Andrykowski
Journal:  J Behav Med       Date:  2014-12-23

4.  Comparison of the screening practices of unaffected noncarriers under 40 and between 40 and 49 in BRCA1/2 families.

Authors:  Christelle Duprez; Véronique Christophe; Isabelle Milhabet; Aurélie Krzeminski; Claude Adenis; Pascaline Berthet; Jean-Philippe Peyrat; Philippe Vennin
Journal:  J Genet Couns       Date:  2013-01-25       Impact factor: 2.537

5.  BRCA 1 & 2 mutations in Sudanese secondary school girls with known breast cancer in their families.

Authors:  Ahmed M Elnour; Abozer Y Elderdery; Jeremy Mills; Babiker A Mohammed; Daw Elbietabdelaal; Abdelraheem Osman Mohamed; Kamal Eldin H Elhassan; Abdel Hady A; Abdel Wahab; Alan Cooper
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6.  No evidence of excessive cancer screening in female noncarriers from BRCA1/2 mutation-positive families.

Authors:  S Guedaoura; S Pelletier; W D Foulkes; P Hamet; J Simard; N Wong; Z El Haffaf; J Chiquette; M Dorval
Journal:  Curr Oncol       Date:  2017-12-20       Impact factor: 3.677

7.  Clinical follow-up and breast and ovarian cancer screening of true BRCA1/2 noncarriers: a qualitative investigation.

Authors:  Sylvie Pelletier; Nora Wong; Zaki El Haffaf; William D Foulkes; Jocelyne Chiquette; Pavel Hamet; Jacques Simard; Michel Dorval
Journal:  Genet Med       Date:  2015-11-05       Impact factor: 8.822

8.  Experience of BRCA1/2 mutation-negative young women from families with hereditary breast and ovarian cancer: a qualitative study.

Authors:  Lynn Macrae; Alicia Navarro de Souza; Carmen G Loiselle; Nora Wong
Journal:  Hered Cancer Clin Pract       Date:  2013-10-16       Impact factor: 2.857

  8 in total

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