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Prospective study of high-risk, BRCA1/2-mutation negative women: the 'negative study'.
Kotsopoulos, Joanne; Metcalfe, Kelly; Alston, Jill; Nikitina, Dina; Ginsburg, Ophira; Eisen, Andrea; Demsky, Rochelle; Akbari, Mohammad; Zbuk, Kevin; Narod, Steven A.
Afiliación
  • Kotsopoulos J; Familial Breast Cancer Unit, Women's College Research Institute, 790 Bay St, 7th Floor, Toronto, ON M5G 1 N8, Canada. joanne.kotsopoulos@wchospital.ca.
BMC Cancer ; 14: 221, 2014 Mar 25.
Article en En | MEDLINE | ID: mdl-24667084
ABSTRACT

BACKGROUND:

We previously reported that women from high-risk families who tested negative for a BRCA1 or BRCA2 (BRCA1/2) mutation were four times more likely to develop breast cancer compared to women in the general population. Preventive measures and risk factors for breast cancer development in these high-risk women have not been evaluated to the same extent as BRCA1/2 positive women. Further, there is virtually no scientific evidence about best practices in their management and care. The proposed study will examine a role of genetic and non-genetic factors and develop the systems and parameters for the monitoring and surveillance necessary to help establish guidelines for the care of this high-risk population. METHODS/

DESIGN:

To achieve our goals, we will assemble and follow a Canadian cohort of 1,000 cancer-free women with a strong family history breast cancer (defined as two or more relatives affected by breast cancer under the age of 50, or three or more relatives diagnosed with breast cancer at any age from one side of the family and with no BRCA1/2 mutation in the family). All eligible participants will be mailed a study package including invitation to participate, consent form, a research questionnaire to collect data regarding family history, reproductive and lifestyle factors, as well as screening and surgery. Usual dietary intake will be assessed by a diet history questionnaire. Biological samples including toenail clippings, urine and blood samples will be collected. These women will be followed every two years by questionnaire to update exposure information, screening practices, surgical and chemoprevention, and disease development.

DISCUSSION:

Findings from this study will serve to help establish clinical guidelines for the implementation of prevention, counseling, and treatment practices for women who face an elevated risk of breast cancer due to family history, but who do not carry a BRCA1/2 mutation.
Asunto(s)

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Contexto en salud: 2_ODS3 Problema de salud: 2_muertes_prematuras_enfermedades_notrasmisibles Asunto principal: Neoplasias de la Mama / Proteína BRCA1 / Predisposición Genética a la Enfermedad / Proteína BRCA2 Tipo de estudio: Etiology_studies / Guideline / Observational_studies / Qualitative_research / Risk_factors_studies Límite: Adult / Female / Humans / Middle aged País/Región como asunto: America do norte Idioma: En Revista: BMC Cancer Asunto de la revista: NEOPLASIAS Año: 2014 Tipo del documento: Article País de afiliación: Canadá

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Contexto en salud: 2_ODS3 Problema de salud: 2_muertes_prematuras_enfermedades_notrasmisibles Asunto principal: Neoplasias de la Mama / Proteína BRCA1 / Predisposición Genética a la Enfermedad / Proteína BRCA2 Tipo de estudio: Etiology_studies / Guideline / Observational_studies / Qualitative_research / Risk_factors_studies Límite: Adult / Female / Humans / Middle aged País/Región como asunto: America do norte Idioma: En Revista: BMC Cancer Asunto de la revista: NEOPLASIAS Año: 2014 Tipo del documento: Article País de afiliación: Canadá
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