公众对新兴癌症筛查方式的偏好:对离散选择实验的系统回顾。

IF 3.1 3区 医学 Q1 HEALTH CARE SCIENCES & SERVICES
Chee Ern Har, Qi Gao, Wenjia Chen, Yi Wang
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引用次数: 0

摘要

背景:早期发现癌症可以降低死亡率和发病率,但传统的筛查方法往往面临诸如侵入性、可及性有限和资源需求高等挑战。新兴的癌症筛查技术可以克服这些障碍,但它们的采用在很大程度上取决于公众的接受程度。本系统综述综合了来自离散选择实验(DCE)研究的证据,这些研究考察了人们对新兴癌症筛查技术的偏好。方法:按照系统评价和荟萃分析的首选报告项目(PRISMA)指南进行系统评价。系统检索了PubMed、Embase、Scopus、Web of Science和EconLit到2025年8月发表的研究。符合条件的研究使用dce来评估对各种模式的偏好,包括液体活检、多种癌症早期检测、人工智能阅读系统、遗传和基因组测试、移动健康应用、基于纳米颗粒的筛查和呼吸分析。研究由两名审稿人独立筛选,并使用DIRECT检查表评估报告质量。使用描述性统计和叙述性综合对数据进行总结。结果:共纳入2014年至2025年间发表的23项研究,大多数集中于基因组检测(n = 8)或液体活检(n = 5)。在所有研究中,确定了32个属性,并根据临床风险、模式特征、筛选过程、结果或伦理考虑进行了分类。答复者普遍赞成临床有效、可获得和破坏性最小的筛查方案。敏感度通常被认为是最具影响力的属性。确定了影响公众偏好的特定模式属性,包括基因和基因组测试的数据隐私和可保性,以及移动健康技术和人工智能筛查工具的测试提供商的作用。在许多研究中观察到偏好、属性重要性和预测摄取的异质性,突出了人群中对癌症筛查和模式特定属性的不同态度。结论:本系统综述首次综合了多种新兴癌症筛查技术的DCE证据。研究结果表明,公众的偏好不仅受到临床表现的影响,还受到便利性、成本和新模式的感知可信度的影响。偏好的相当大的异质性表明需要有针对性的策略来吸引不同的人口亚群,并避免在吸收方面扩大差距。随着这些技术走向临床应用,强有力的治理和监管保障对于确保将其转化为公平和有效的癌症筛查规划至关重要。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Public Preferences for Emerging Cancer Screening Modalities: A Systematic Review of Discrete Choice Experiments.

Background: Early detection of cancer reduces mortality and morbidity, but conventional screening methods often face challenges such as invasiveness, limited accessibility and high resource demands. Emerging cancer screening technologies could overcome these barriers, yet their adoption depends heavily on public acceptance. This systematic review synthesises evidence from discrete choice experiment (DCE) studies examining population preferences for emerging cancer screening technologies.

Methods: A systematic review was conducting following the Preferred Reporting Items for Systematic Reviews and Meta-Analyses (PRISMA) guidelines. PubMed, Embase, Scopus, Web of Science and EconLit were systematically searched for studies published up to August 2025. Eligible studies employed DCEs to assess preferences for modalities including liquid biopsy, multi-cancer early detection tests, artificial intelligence reading systems, genetic and genomic testing, mobile Health applications, nanopill-based screening and breath analysis. Studies were screened independently by two reviewers and assessed for reporting quality using the DIRECT checklist. Data were summarised using descriptive statistics and narrative synthesis.

Results: In total, 23 studies published between 2014 and 2025 were included, most focusing on genomic testing (n = 8) or liquid biopsy (n = 5). Across studies, 32 attributes were identified and categorised under clinical risk, modality characteristics, screening process, outcomes, or ethical considerations. Respondents generally favoured screening programmes that were clinically effective, accessible and minimally disruptive. Sensitivity was most frequently reported as the most influential attribute. Modality specific attributes influencing public preferences were identified, including data privacy and insurability for genetic and genomic testing, and the role of test providers for mHealth technologies and AI screening tools. Heterogeneity in preferences, attribute importance and predicted uptake were observed across many studies, highlighting differential attitudes towards cancer screening and modality specific attributes within the population.

Conclusions: This systematic review provides the first synthesis of DCE evidence across a wide range of emerging cancer screening technologies. Findings reveal that public preferences were shaped not only by clinical performance, but also by convenience, cost and the perceived credibility of new modalities. Considerable heterogeneity in preferences signals the need for tailored strategies to engage different population subgroups and avoid widening disparities in uptake. As these technologies move towards clinical adoption, robust governance and regulatory safeguards will be essential to ensure their translation into equitable and effective cancer screening programmes.

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来源期刊
Patient-Patient Centered Outcomes Research
Patient-Patient Centered Outcomes Research HEALTH CARE SCIENCES & SERVICES-
CiteScore
6.60
自引率
8.30%
发文量
44
审稿时长
>12 weeks
期刊介绍: The Patient provides a venue for scientifically rigorous, timely, and relevant research to promote the development, evaluation and implementation of therapies, technologies, and innovations that will enhance the patient experience. It is an international forum for research that advances and/or applies qualitative or quantitative methods to promote the generation, synthesis, or interpretation of evidence. The journal has specific interest in receiving original research, reviews and commentaries related to qualitative and mixed methods research, stated-preference methods, patient reported outcomes, and shared decision making. Advances in regulatory science, patient-focused drug development, patient-centered benefit-risk and health technology assessment will also be considered. Additional digital features (including animated abstracts, video abstracts, slide decks, audio slides, instructional videos, infographics, podcasts and animations) can be published with articles; these are designed to increase the visibility, readership and educational value of the journal’s content. In addition, articles published in The Patient may be accompanied by plain language summaries to assist readers who have some knowledge of, but not in-depth expertise in, the area to understand important medical advances. All manuscripts are subject to peer review by international experts.
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