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Societal views on using risk-based innovations to inform cancer screening and referral policies: findings from three community juries.

Accepted version
Peer-reviewed

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Abstract

BACKGROUND: Recent advances mean that innovations are emerging that enable better stratification of individuals based on their risk of cancer so that screening or diagnostic investigations can be targeted to those at greatest need. We explored the views of the public, from a societal perspective, of using such risk-based innovations to identify people's cancer risk and allocating healthcare accordingly. METHODS: We conducted three community juries, each with 7-9 participants. Participants were informed about the topic and potential novel risk-based innovations through a series of presentations from experts and discussions. Polygenic risk scores, geodemographic segmentation, continuous monitoring of biomarkers, minimally invasive tests, artificial intelligence analysis of medical records, and wearable devices were used as examples. The participants then deliberated over the research questions before reporting their verdicts on the acceptability of these novel data-based approaches in principle. Transcripts were analysed using codebook thematic analysis. RESULTS: All juries found that the proposed risk-based approaches to cancer healthcare were, in general, acceptable. Primarily this was because the approaches would enable use of information in a positive and constructive way. However, there were a number of qualifiers or caveats. In particular, participants highlighted the necessity of using accurate and robust data with a well-evidenced association with cancer risk. They also expressed concerns about unintended consequences such as for insurance, scams or erosion of personal liberty, and the burden to participate in data collection across society. All agreed that opting-out must be straightforward. CONCLUSIONS: Informed members of the public supported the concept of using innovations to estimate cancer risk and inform healthcare. Their priorities for accuracy, data security, participation burden, and personal liberty and choice tended to overlap with those of developers and policymakers. Work to ready these innovations for implementation should continue, with the public's priorities accounted for in their development and dissemination in order to address any unintended consequences upfront.

Description

Journal Title

BMC Public Health

Conference Name

Journal ISSN

1472-698X
1471-2458

Volume Title

Publisher

Springer Nature

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Except where otherwised noted, this item's license is described as Attribution 4.0 International
Sponsorship
Cancer Research UK (PICATR-2022/100003)
This research was funded by a Cancer Research UK commissioned research award (reference PICATR-2022/100003). Juliet Usher-Smith, Advanced Fellow, NIHR300861, is funded by the National Institute for Health and Care Research for this research project. Rebecca Dennison was also funded on this NIHR fellowship. 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.

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