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从肿瘤活检组织的所有权到监管权:基因组检测中患者观点的混合方法研究。

From ownership to custodianship of tumor biopsy tissue in genomic testing: a mixed methods study of patient views.

机构信息

Institute for Ethics and Society, The University of Notre Dame Australia, Broadway, NSW, Australia.

Psycho-Oncology Co-operative Research Group, School of Psychology, University of Sydney, Sydney, NSW, Australia.

出版信息

Oncologist. 2024 Sep 6;29(9):e1169-e1179. doi: 10.1093/oncolo/oyae074.

Abstract

Tumor mutation profiling (MP) is often conducted on tissue from biopsies conducted for clinical purposes (diagnostic tissue). We aimed to explore the views of patients with cancer on who should own tumor biopsy tissue, pay for its storage, and decide on its future use; and determine their attitudes to and predictors of undergoing additional biopsies if required for research purposes. In this mixed methods, cross-sectional study, patients with advanced solid cancers enrolled in the Molecular Screening and Therapeutics Program (n = 397) completed a questionnaire prior to undergoing MP (n = 356/397). A subset (n = 23) also completed a qualitative interview. Fifty percent of participants believed they and/or relatives should own and control access to diagnostic tissue. Most (65.5%) believed the government should pay for tissue preparation. Qualitative themes included (1) custodianship of diagnostic tissue, (2) changing value of tissue across time and between cultures, (3) equity regarding payment, and (4) cost-benefit considerations in deciding on additional biopsies. Policy and regulation should consider patient perspectives. Extension of publicly funded health care to include tissue retrieval for clinical trials should be considered.

摘要

肿瘤突变分析(MP)通常在为临床目的(诊断组织)进行的活检组织上进行。我们旨在探讨癌症患者对谁应该拥有肿瘤活检组织、支付其储存费用以及决定其未来用途的看法;并确定他们对为研究目的进行额外活检的态度和预测因素。在这项混合方法的横断面研究中,参加分子筛查和治疗计划的晚期实体癌患者(n=397)在进行 MP 之前完成了一份问卷(n=356/397)。一小部分(n=23)还完成了定性访谈。50%的参与者认为他们和/或亲属应该拥有并控制对诊断性组织的访问权。大多数(65.5%)人认为政府应该支付组织准备的费用。定性主题包括(1)诊断性组织的保管权,(2)组织在不同时间和文化之间的价值变化,(3)关于支付的公平性,以及(4)在决定是否进行额外活检时的成本效益考虑。政策和法规应考虑患者的观点。应考虑将公共资助的医疗保健扩展到包括临床试验的组织检索。

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