Literature DB >> 17346477

Clinical management recommendations for surveillance and risk-reduction strategies for hereditary breast and ovarian cancer among individuals carrying a deleterious BRCA1 or BRCA2 mutation.

Doug Horsman1, Brenda J Wilson, Denise Avard, Wendy S Meschino, Charmaine Kim Sing, Marie Plante, Andrea Eisen, Heather E Howley, Jacques Simard.   

Abstract

BACKGROUND: In Canada, there are wide variations in services for patients at risk for hereditary breast and ovarian cancer (HBOC), and clinical interventions and recommendations differ between regions and/or provinces. National strategies for the clinical management of HBOC exist in the United Kingdom, France, and Australia, and clinical programs in Canada would benefit from similar national recommendations and a consistent approach to clinical management. The National Hereditary Cancer Task Force developed recommendations to address the clinical management of patients at high risk of HBOC and related cancers. These recommendations are based on current practice in high-risk cancer clinics that provide care for individuals with known BRCA1 or BRCA2 mutations.
METHODS: Canadian consensus recommendations were generated by the National Hereditary Cancer Task Force and compared mainly with two recently published guidance documents on the clinical management of women with increased risk of HBOC, one from the United Kingdom and the other from France. After review of these documents and the associated supporting scientific evidence, the Canadian consensus recommendations were modified and rated using predefined criteria.
CONCLUSIONS: These recommendations pertain to (1) surveillance options including breast self-examination, clinical breast examination, breast surveillance by imaging, ovarian cancer surveillance, and surveillance for men; (2) risk-reduction strategies including prophylactic mastectomy, prophylactic salpingo-oophorectomy, and pharmacoprevention; and (3) the use of exogenous hormones. Regular updates should occur as new evidence becomes available.

Entities:  

Mesh:

Year:  2007        PMID: 17346477     DOI: 10.1016/s1701-2163(16)32349-0

Source DB:  PubMed          Journal:  J Obstet Gynaecol Can        ISSN: 1701-2163


  21 in total

1.  French women's breast self-examination practices with time after undergoing BRCA1/2 genetic testing.

Authors:  C Maheu; T Apostolidis; A Petri-Cal; E Mouret-Fourme; M Gauthier-Villars; C Lasset; P Berthet; J-P Fricker; O Caron; E Luporsi; L Gladieff; C Noguès; C Julian-Reynier
Journal:  Fam Cancer       Date:  2012-06       Impact factor: 2.375

2.  [Guideline for the prevention and early detection of breast and ovarian cancer in high risk patients, particularly in women from HBOC (hereditary breast and ovarian cancer) families].

Authors:  Christian F Singer; Muy-Kheng Tea; Gunda Pristauz; Michael Hubalek; Christine Rappaport; Christopher Riedl; Thomas Helbich
Journal:  Wien Klin Wochenschr       Date:  2012-05-28       Impact factor: 1.704

3.  Should physicians warn patients' relatives of genetic risks?

Authors:  Mireille Lacroix; Gillian Nycum; Béatrice Godard; Bartha Maria Knoppers
Journal:  CMAJ       Date:  2008-02-26       Impact factor: 8.262

4.  Perspectives of Women Considering Bilateral Prophylactic Mastectomy and their Peers towards a Telephone-Based Peer Support Intervention.

Authors:  D St-Pierre; K Bouchard; L Gauthier; J Chiquette; Michel Dorval
Journal:  J Genet Couns       Date:  2017-09-15       Impact factor: 2.537

Review 5.  Breast reconstruction following prophylactic or therapeutic mastectomy for breast cancer: Recommendations from an evidence-based provincial guideline.

Authors:  Melissa Shea-Budgell; May Lynn Quan; Blair Mehling; Claire Temple-Oberle
Journal:  Plast Surg (Oakv)       Date:  2014       Impact factor: 0.947

6.  Preserving the self: the process of decision making about hereditary breast cancer and ovarian cancer risk reduction.

Authors:  A Fuchsia Howard; Lynda G Balneaves; Joan L Bottorff; Patricia Rodney
Journal:  Qual Health Res       Date:  2010-10-27

7.  Multimodality breast cancer screening in women with a familial or genetic predisposition.

Authors:  I Trop; L Lalonde; M H Mayrand; J David; N Larouche; D Provencher
Journal:  Curr Oncol       Date:  2010-06       Impact factor: 3.677

8.  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

9.  Impact of familial risk and mammography screening on prognostic indicators of breast disease among women from the Ontario site of the Breast Cancer Family Registry.

Authors:  Meghan J Walker; Lucia Mirea; Kristine Cooper; Mitra Nabavi; Gord Glendon; Irene L Andrulis; Julia A Knight; Frances P O'Malley; Anna M Chiarelli
Journal:  Fam Cancer       Date:  2014-06       Impact factor: 2.375

10.  Is the psychological impact of genetic testing moderated by support and sharing of test results to family and friends?

Authors:  Julie Lapointe; Michel Dorval; Catherine Noguès; Roxane Fabre; Claire Julian-Reynier
Journal:  Fam Cancer       Date:  2013-12       Impact factor: 2.375

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