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Breast cancer risk assessment for prescription of menopausal hormone therapy in women with a family history of breast cancer: an epidemiological modelling study.
Huntley, Catherine; Torr, Bethany; Kavanaugh, Grace; George, Angela; Hanson, Helen; Snape, Katie; Broggio, John; Glasgow, Louise; Tischkowitz, Marc; Evans, D Gareth; Antoniou, Antonis C; Turnbull, Clare.
Afiliação
  • Huntley C; Division of Genetics and Epidemiology, Institute of Cancer Research, London; National Cancer Registration and Analysis Service, National Disease Registration Service, NHS England, London.
  • Torr B; Division of Genetics and Epidemiology, Institute of Cancer Research, London.
  • Kavanaugh G; Division of Genetics and Epidemiology, Institute of Cancer Research, London.
  • George A; Division of Genetics and Epidemiology, Institute of Cancer Research, London; Royal Marsden NHS Foundation Trust, London.
  • Hanson H; Division of Genetics and Epidemiology, Institute of Cancer Research, London; Peninsula Regional Genetics Service, Royal Devon University Healthcare NHS Foundation Trust, Exeter; Department of Clinical and Biomedical Sciences, University of Exeter Medical School, Exeter.
  • Snape K; South West Thames Regional Genetics Service, St George's University Hospitals NHS Foundation Trust, London; St George's University of London, London.
  • Broggio J; National Cancer Registration and Analysis Service, National Disease Registration Service, NHS England, London.
  • Glasgow L; Village Health Group Primary Care Practice, Nottingham.
  • Tischkowitz M; Department of Medical Genetics, National Institute for Health Research, Cambridge Biomedical Research Centre, University of Cambridge, Cambridge.
  • Evans DG; Division of Evolution, Infection and Genomics, University of Manchester, Manchester; Manchester Centre for Genomic Medicine and North West Laboratory Genetics Hub, Manchester University NHS Foundation Trust, Manchester Academic Health Science Centre, Manchester.
  • Antoniou AC; Centre for Cancer Genetic Epidemiology, Department of Public Health and Primary Care, University of Cambridge, Cambridge.
  • Turnbull C; Division of Genetics and Epidemiology, Institute of Cancer Research, London; National Cancer Registration and Analysis Service, National Disease Registration Service, NHS England, London; Royal Marsden NHS Foundation Trust, London.
Br J Gen Pract ; 2024 Jul 08.
Article em En | MEDLINE | ID: mdl-38724186
ABSTRACT

BACKGROUND:

Menopausal hormone therapy (MHT) can alleviate menopausal symptoms but has been associated with an increased risk of breast cancer. MHT prescription should be preceded by individualised risk/benefit evaluation; however, data outlining the impact of family history alongside different MHT therapeutic approaches are lacking.

AIM:

To quantify the risks associated with MHT use in women with varying breast cancer family histories of developing and dying from breast cancer. DESIGN AND

SETTING:

An epidemiological modelling study for women in England using the BOADICEA breast cancer prediction model and data relating to MHT use and breast cancer risk taken from research by the Collaborative Group on Hormonal Factors in Breast Cancer.

METHOD:

The risk of developing and dying from breast cancer between the ages of 50 and 80 years was modelled in women with four different breast cancer family history profiles 'average', 'modest', 'intermediate', and 'strong' by using 1) background risks of breast cancer by age and family history, 2) relative risks for breast cancer associated with MHT use, and 3) 10-year breast cancer-specific net mortality rates. This study modelled use of combined oestrogen-progestogen MHT (cyclical or continuous) and oestrogen-only MHT.

RESULTS:

For a woman of 'average' family history taking no MHT, the cumulative breast cancer risk (age 50-80 years) is 9.8%, and the risk of dying from the breast cancer is 1.7%. In this model, 5 years' exposure to combined-cyclical MHT (age 50-55 years) was calculated to increase these risks to 11.0% and 1.8%, respectively. For a woman with a 'strong' family history taking no MHT, the cumulative breast cancer risk is 19.6% (age 50-80 years), and the risk of dying from the breast cancer is 3.2%. With 5 years' exposure to MHT (age 50-55 years), this model showed that these risks increase to 22.4% and 3.5%, respectively.

CONCLUSION:

In this model, both family history and MHT are associated with increased risk of breast cancer. Estimates of the risks of breast cancer associated with MHT for women with different family histories can be used to support decision making around MHT prescription for women experiencing menopausal symptoms.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Ano de publicação: 2024 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Ano de publicação: 2024 Tipo de documento: Article