Privacy, Policy, and Profits: Survey of Patient Preferences for Research on De-Identified Biosamples.

IF 1.1
Amelia J Hood, Mario Macis, Diana Mendoza Cervantes, Todd Bear, Jeffrey Kahn, Jennifer Xavier, Adrian Lee, Ananya Dewan, Marielle S Gross
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Abstract

This study aims to identify patient preferences to inform ethical frameworks, policies, and technologies for advancing biobanking and precision medicine while balancing competing objectives and priorities. We surveyed 109 American breast cancer patients in 2022 about conditions for receiving research results, how their biospecimens are used, partnerships between nonprofit health systems and for-profit companies, and the distribution of financial returns from research. Survey questions explored the balance between objectives like maintaining de-identification versus receiving research results and other benefits. Patients in our sample generally prefer to be re-identified to receive information about the use of their donated tissue-especially research results. They support public-private partnerships if they speed up new therapies and favor the idea of sharing in financial returns generated from research on their tissue. These insights can inform the development of frameworks and technologies that position patients as key stakeholders in biobanking research.

隐私、政策和利润:对去识别生物样本研究的患者偏好的调查。
本研究旨在确定患者的偏好,为推进生物银行和精准医学的伦理框架、政策和技术提供信息,同时平衡相互竞争的目标和优先事项。我们在2022年对109名美国乳腺癌患者进行了调查,内容涉及接受研究结果的条件、他们的生物标本是如何使用的、非营利卫生系统与营利性公司之间的合作关系,以及研究的经济回报分布。调查问题探讨了维持去识别与接受研究结果和其他利益等目标之间的平衡。我们样本中的患者通常更愿意被重新识别,以获得有关其捐赠组织使用的信息,尤其是研究结果。如果能加快新疗法的发展,他们支持公私合作,并赞成分享组织研究产生的经济回报的想法。这些见解可以为框架和技术的发展提供信息,将患者定位为生物银行研究的关键利益相关者。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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