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Proactive breast cancer risk assessment in primary care: a review based on the principles of screening.

Accepted version
Peer-reviewed

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Abstract

In the UK, the National Institute for Health and Care Excellence (NICE) recommends that women at moderate or high risk of breast cancer be offered risk-reducing medication and enhanced breast screening/surveillance. In June 2022, NICE withdrew a statement recommending assessment of risk in primary care only when women present with concerns. This shift to the proactive assessment of risk substantially changes the role of primary care, in effect paving the way for a primary care-based screening programme to identify those at moderate or high risk of breast cancer. In this article, we review the literature surrounding proactive breast cancer risk assessment within primary care against the consolidated framework for screening. We find that risk assessment for women under 50 years currently satisfies many of the standard principles for screening. Most notably, there are large numbers of women at moderate or high risk currently unidentified, risk models exist that can identify those women with reasonable accuracy, and management options offer the opportunity to reduce breast cancer incidence and mortality in that group. However, there remain a number of uncertainties and research gaps, particularly around the programme/system requirements, that need to be addressed before these benefits can be realised.

Description

Journal Title

Br J Cancer

Conference Name

Journal ISSN

0007-0920
1532-1827

Volume Title

Publisher

Springer Science and Business Media LLC

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Except where otherwised noted, this item's license is described as All Rights Reserved
Sponsorship
Department of Health (via National Institute for Health Research (NIHR)) (NIHR300861)
National Institute for Health Research (IS-BRC-1215-20014)
Juliet A Usher-Smith and Rebecca Dennison are funded by an Advanced Fellowship from the National Institute for Health and Social Care Research (NIHR300861). Sarah Hindmarch is funded by a Manchester Cancer Research Centre PhD studentship. David French is supported by the NIHR Manchester Biomedical Research Centre (IS-BRC-1215-20007). Marc Tischkowitz was supported by the NIHR Cambridge Biomedical Research Centre (BRC-1215-20014). Fiona M Walter is Director and Jon Emery is Associate Director of the multi-institutional CanTest Collaborative, which is funded by Cancer Research UK (C8640/A23385). Stephanie Archer and Francisca Stuzin are funded by a Cancer Research UK programme grant (PPRPGM-Nov20\100002). ). Jon Emery is supported by an NHMRC Investigator grant (APP1195302). The University of Cambridge has received salary support for Douglas F Easton from the NHS in the East of England through the Clinical Academic Reserve. The views expressed in this publication are those of the author(s) and not necessarily those of the NIHR, NHS or the UK Department of Health and Social Care.