Ethical, legal, and social issues related to genetics and genomics in cancer: A scoping review and narrative synthesis

被引:0
|
作者
Smit, Amelia K. [1 ,2 ]
Gokoolparsadh, Akira [3 ]
McWhirter, Rebekah [4 ]
Newett, Lyndsay [5 ]
Milch, Vivienne [6 ,7 ]
Hermes, Azure [5 ]
McInerney-Leo, Aideen [8 ]
Newson, Ainsley J. [3 ]
机构
[1] Univ Sydney, Daffodil Ctr, Sydney, NSW, Australia
[2] Univ Sydney, Fac Med & Hlth, Sydney Sch Publ Hlth, Sydney, NSW, Australia
[3] Univ Sydney, Fac Med & Hlth, Sydney Sch Publ Hlth, Sydney Hlth Eth, Edward Ford Bldg A27, Sydney, NSW 2006, Australia
[4] Australian Natl Univ, ANU Coll Law, Canberra, ACT, Australia
[5] Australian Natl Univ, Natl Ctr Indigenous Genom, Canberra, ACT, Australia
[6] Canc Australia, Surry Hills, NSW, Australia
[7] Flinders Univ S Australia, Caring Futures Inst, Adelaide, Australia
[8] Univ Queensland, Frazer Inst, Dermatol Res Ctr, Brisbane, Qld, Australia
基金
澳大利亚国家健康与医学研究理事会; 英国医学研究理事会;
关键词
Bioethics; Genetics; Genomics; Review; PREDISPOSITION; MEDICINE; PRIVACY; CONSENT; IMPACT; RISK;
D O I
10.1016/j.gim.2024.101270
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Genomics is increasingly being incorporated into models of care for cancer. Understanding the ethical, legal, and social issues (ELSI) in this domain is important for successful and equitable implementation. We aimed to identify ELSI scholarship specific to cancer control and genomics. To do this, we undertook a scoping literature review and narrative synthesis, identifying 46 articles that met inclusion criteria. Eighteen ELSI themes were developed, including (1) equity of access, which included structural barriers to testing and research, access to preventive and follow-up care, and engagement with health systems; (2) family considerations, such as an ethical obligation to disseminate relevant genomic information to at-risk family members; (3) legal considerations, including privacy and confidentiality, genetic discrimination, and the prospective duty to reclassify variants; and (4) optimizing consent processes in clinical care and research. Gaps in the literature were identified with respect to equity for people living in rural or remote areas, and how to provide ethical care within culturally, linguistically, and ethnically diverse communities, including First Nations peoples. Our fi ndings suggest a need for a multidisciplinary approach to examining ELSI in cancer genomics beyond initial test indication and within the broader context of the mainstreaming of genomics in health care. Crown Copyright 2024 Published by Elsevier Inc. on behalf of American College of Medical Genetics and Genomics. This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/).
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页数:18
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