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Policy options to facilitate cancer genomic variant data sharing: outcomes of a modified policy Delphi
Sharing cancer gene variant and relevant clinical data could accelerate progress in cancer genomics. However, data sharing is currently impeded by issues related to financial sustainability, equity, incentives, privacy and security, and data quality. Evidence-based policy options to facilitate data...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10347303/ https://www.ncbi.nlm.nih.gov/pubmed/37456713 http://dx.doi.org/10.1093/jlb/lsad022 |
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author | Robinson, Jill O Daoud, Amira Geary, Janis Rahimzadeh, Vasiliki Bollinger, Juli Guerrini, Christi J Cook-Deegan, Robert McGuire, Amy L Majumder, Mary A |
author_facet | Robinson, Jill O Daoud, Amira Geary, Janis Rahimzadeh, Vasiliki Bollinger, Juli Guerrini, Christi J Cook-Deegan, Robert McGuire, Amy L Majumder, Mary A |
author_sort | Robinson, Jill O |
collection | PubMed |
description | Sharing cancer gene variant and relevant clinical data could accelerate progress in cancer genomics. However, data sharing is currently impeded by issues related to financial sustainability, equity, incentives, privacy and security, and data quality. Evidence-based policy options to facilitate data sharing in these domains, and ultimately improve interpretation of cancer-associated genomic variants, are therefore needed. We conducted a modified policy Delphi with expert stakeholders that involved generating, evaluating, and ranking potential policy options to address these issues, with a focus on the US context. We found policy options in the financial sustainability domain were highly ranked, particularly stable funding for trusted entities. However, some Delphi panelists noted that the culture of public research funding has favored short-term grants. Panelists favored policy options focused on action by funders, which had the highest overall total scores that combined effectiveness and feasibility ratings and priority ranking within domains. Panelists also endorsed some policy options connected to actors such as journals, but they were more skeptical of policy options connected to legislative actors and data resources. These findings are critical inputs for policy makers as they consider policies to enable sharing of cancer gene variant data to improve health. |
format | Online Article Text |
id | pubmed-10347303 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-103473032023-07-15 Policy options to facilitate cancer genomic variant data sharing: outcomes of a modified policy Delphi Robinson, Jill O Daoud, Amira Geary, Janis Rahimzadeh, Vasiliki Bollinger, Juli Guerrini, Christi J Cook-Deegan, Robert McGuire, Amy L Majumder, Mary A J Law Biosci Original Article Sharing cancer gene variant and relevant clinical data could accelerate progress in cancer genomics. However, data sharing is currently impeded by issues related to financial sustainability, equity, incentives, privacy and security, and data quality. Evidence-based policy options to facilitate data sharing in these domains, and ultimately improve interpretation of cancer-associated genomic variants, are therefore needed. We conducted a modified policy Delphi with expert stakeholders that involved generating, evaluating, and ranking potential policy options to address these issues, with a focus on the US context. We found policy options in the financial sustainability domain were highly ranked, particularly stable funding for trusted entities. However, some Delphi panelists noted that the culture of public research funding has favored short-term grants. Panelists favored policy options focused on action by funders, which had the highest overall total scores that combined effectiveness and feasibility ratings and priority ranking within domains. Panelists also endorsed some policy options connected to actors such as journals, but they were more skeptical of policy options connected to legislative actors and data resources. These findings are critical inputs for policy makers as they consider policies to enable sharing of cancer gene variant data to improve health. Oxford University Press 2023-07-14 /pmc/articles/PMC10347303/ /pubmed/37456713 http://dx.doi.org/10.1093/jlb/lsad022 Text en © The Author(s) 2023. Published by Oxford University Press on behalf of Duke University School of Law, Harvard Law School, Oxford University Press, and Stanford Law School. https://creativecommons.org/licenses/by/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Original Article Robinson, Jill O Daoud, Amira Geary, Janis Rahimzadeh, Vasiliki Bollinger, Juli Guerrini, Christi J Cook-Deegan, Robert McGuire, Amy L Majumder, Mary A Policy options to facilitate cancer genomic variant data sharing: outcomes of a modified policy Delphi |
title | Policy options to facilitate cancer genomic variant data sharing: outcomes of a modified policy Delphi |
title_full | Policy options to facilitate cancer genomic variant data sharing: outcomes of a modified policy Delphi |
title_fullStr | Policy options to facilitate cancer genomic variant data sharing: outcomes of a modified policy Delphi |
title_full_unstemmed | Policy options to facilitate cancer genomic variant data sharing: outcomes of a modified policy Delphi |
title_short | Policy options to facilitate cancer genomic variant data sharing: outcomes of a modified policy Delphi |
title_sort | policy options to facilitate cancer genomic variant data sharing: outcomes of a modified policy delphi |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10347303/ https://www.ncbi.nlm.nih.gov/pubmed/37456713 http://dx.doi.org/10.1093/jlb/lsad022 |
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