Improving our model of cascade testing for hereditary cancer risk by leveraging patient peer support: a concept report.

IF 2 4区 医学 Q3 ONCOLOGY Hereditary Cancer in Clinical Practice Pub Date : 2021-09-26 DOI:10.1186/s13053-021-00198-7
Suzanne C O'Neill, Jada G Hamilton, Claire C Conley, Beth N Peshkin, Rosalba Sacca, Glynnis A McDonnell, Claudine Isaacs, Mark E Robson, Kenneth P Tercyak
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Abstract

Consensus and evidence suggest that cascade testing is critical to achieve the promise of cancer genetic testing. However, barriers to cascade testing include effective family communication of genetic risk information and family members' ability to cope with genetic risk. These barriers are further complicated by the developmental needs of unaffected family members during critical windows for family communication and adaptation. Peer support could address these barriers. We provide two illustrative examples of ongoing BRCA1/2-related clinical trials that apply a peer support model to improve family communication and functioning. Peer support can augment currently available genetic services to facilitate adjustment to and effective use of cancer genetic risk information. Importantly, this scalable approach can address the presence of cancer risk within families across multiple developmental stages. This applies a family-centered perspective that accommodates all potentially at-risk relatives. This peer support model can be further applied to emerging topics in clinical genetics to expand reach and impact.

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利用患者同伴支持改进我们的遗传性癌症风险级联检测模式:概念报告。
共识和证据表明,级联检测对于实现癌症基因检测的承诺至关重要。然而,级联检测的障碍包括遗传风险信息的有效家庭沟通以及家庭成员应对遗传风险的能力。在家庭沟通和适应的关键窗口期,未受影响家庭成员的发展需求使这些障碍变得更加复杂。同伴支持可以解决这些障碍。我们提供了两个正在进行的 BRCA1/2 相关临床试验的示例,这些试验采用同伴支持模式来改善家庭沟通和功能。同伴支持可以增强目前可用的遗传服务,以促进对癌症遗传风险信息的适应和有效利用。重要的是,这种可扩展的方法可以解决家庭在多个发展阶段中存在的癌症风险问题。这就采用了以家庭为中心的视角,照顾到了所有潜在的高危亲属。这种同伴支持模式可进一步应用于临床遗传学的新兴课题,以扩大覆盖面和影响力。
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来源期刊
CiteScore
3.10
自引率
5.90%
发文量
38
审稿时长
>12 weeks
期刊介绍: Hereditary Cancer in Clinical Practice is an open access journal that publishes articles of interest for the cancer genetics community and serves as a discussion forum for the development appropriate healthcare strategies. Cancer genetics encompasses a wide variety of disciplines and knowledge in the field is rapidly growing, especially as the amount of information linking genetic differences to inherited cancer predispositions continues expanding. With the increased knowledge of genetic variability and how this relates to cancer risk there is a growing demand not only to disseminate this information into clinical practice but also to enable competent debate concerning how such information is managed and what it implies for patient care. Topics covered by the journal include but are not limited to: Original research articles on any aspect of inherited predispositions to cancer. Reviews of inherited cancer predispositions. Application of molecular and cytogenetic analysis to clinical decision making. Clinical aspects of the management of hereditary cancers. Genetic counselling issues associated with cancer genetics. The role of registries in improving health care of patients with an inherited predisposition to cancer.
期刊最新文献
BRCA2 germline mutation carrier with five malignancies: a case report. A genome-wide association study in Swedish colorectal cancer patients with gastric- and prostate cancer in relatives. Breast cancer and ATM mutations: treatment implications. Meeting abstracts from the Annual Conference "Clinical Genetics of Cancer 2023". Validation of a guidelines-based digital tool to assess the need for germline cancer genetic testing.
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