Facilitating Equitable Access to Genomic Testing for Advanced Cancer: A Combined Intuition and Theory-Informed Approach to Intervention Development and Deployment.

IF 1.3 4区 医学 Q4 GENETICS & HEREDITY
Public Health Genomics Pub Date : 2025-01-01 Epub Date: 2025-03-11 DOI:10.1159/000544946
Rona Weerasuriya, Joseph Elias, Melissa Martyn, Sophie O'Haire, Clara Gaff, Kortnye Smith, Jayesh Desai, Natalie Taylor
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引用次数: 0

Abstract

Introduction: Rapid advancements in genomic testing have revolutionised cancer care diagnostics and treatment. However, keeping pace with the evolving genomics knowledge is a challenge for oncologists who are not genomic experts. This detrimentally impacts on equitable patient access to related services and benefits which require training in genomics. In Australia, cancer incidence, survival, and mortality rates are significantly worse in the most socioeconomically disadvantaged areas compared to the least disadvantaged areas. Guided by implementation science methods, the research aimed to determine how to support oncologists with varying levels of genomic expertise to tailor optimal treatment decisions and deliver a high-quality service, across diverse geographical locations.

Methods: We used a novel approach combining clinician intuition and implementation science theory to co-design service interventions (i.e., service models) and associated implementation strategies to inform operationalisation. Phenomenology and principles of co-design guided two phases of data collection with two separate cohorts of oncologists delivering care to advanced cancer patients. Phase 1 interview data were coded thematically to develop the service models, while phase 2 focus group data were used to identify implementation strategies to support service model operationalisation. The Consolidated Framework for Implementation Research (CFIR) informed phase 1 and 2 data analysis.

Results: Phase 1 established three overarching themes and nine subthemes: (1) access - potential for inequitable patient access by centralising genomic expertise, (2) indicators for test use - identifying suitable patients for complex genomic profiling (CGP) testing, and (3) supporting use of results - confidence to discuss results, particularly from germline and somatic testing. Five challenges were prioritised, mapped to the CGP clinical pathway, and coded to 11 unique CFIR constructs. Across all five prioritised challenges, we recorded 19 intuitive and generated 21 theory-informed strategies. The development of three service models (i.e., centralised expert, local super user, and point of care resources) arose through considering these strategies in combination with the study teams' broader experiences with the iPREDICT trial. In phase 2, we identified 11 implementation challenges, mapped to 7 CFIR constructs, and 11 intuitive and 20 theory-informed strategies for service model operationalisation.

Conclusion: The service models generated from our study are currently being tested in a multi-centre implementation study to evaluate feasibility, effectiveness, acceptability, sustainability, and scalability.

促进晚期癌症基因组检测的公平获取:干预措施开发和部署的直觉和理论结合方法。
基因组检测的快速发展已经彻底改变了癌症护理诊断和治疗。然而,对于不是基因组学专家的肿瘤学家来说,跟上不断发展的基因组学知识是一个挑战。这对患者公平获得相关服务和福利产生不利影响,这需要基因组学方面的培训。在澳大利亚,社会经济最不利地区的癌症发病率、存活率和死亡率明显低于最不利地区。在实施科学方法的指导下,该研究旨在确定如何支持具有不同水平基因组专业知识的肿瘤学家在不同地点定制最佳治疗决策并提供高质量服务。方法:我们采用一种结合临床医生直觉和实施科学理论的新方法,共同设计服务干预措施(即服务模型)和相关的实施策略,为操作提供信息。现象学和共同设计原则指导了两阶段的数据收集,两组独立的肿瘤学家为晚期癌症患者提供护理。第一阶段的访谈数据按主题进行编码,以开发服务模型,而第二阶段的焦点小组数据用于确定支持服务模型操作化的实现策略。实施研究综合框架(CFIR)为第一阶段和第二阶段的数据分析提供了信息。结果:第一阶段建立了三个总体主题和九个子主题:(1)获取-通过集中基因组专业知识可能导致不公平的患者获取;(2)检测使用指标-确定适合进行综合基因组图谱(CGP)检测的患者;(3)支持结果使用-讨论结果的信心,特别是生殖系和体细胞检测。五个挑战被优先考虑,映射到CGP临床途径,并编码为11个独特的CFIR结构。在所有五个优先挑战中,我们记录了19个直觉策略,并生成了21个基于理论的策略。三种服务模式(即集中专家、本地超级用户和护理点资源)的发展是通过考虑这些策略与研究团队在iPREDICT试验中的广泛经验相结合而产生的。在第二阶段,我们确定了11个实现挑战,映射到7个CFIR结构,以及11个直观和20个理论支持的服务模型操作策略。结论:从我们的研究中产生的服务模式目前正在一个多中心实施研究中进行测试,以评估2025年的可行性、有效性、可接受性、可持续性和可扩展性。
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来源期刊
Public Health Genomics
Public Health Genomics 医学-公共卫生、环境卫生与职业卫生
CiteScore
2.90
自引率
0.00%
发文量
14
审稿时长
>12 weeks
期刊介绍: ''Public Health Genomics'' is the leading international journal focusing on the timely translation of genome-based knowledge and technologies into public health, health policies, and healthcare as a whole. This peer-reviewed journal is a bimonthly forum featuring original papers, reviews, short communications, and policy statements. It is supplemented by topic-specific issues providing a comprehensive, holistic and ''all-inclusive'' picture of the chosen subject. Multidisciplinary in scope, it combines theoretical and empirical work from a range of disciplines, notably public health, molecular and medical sciences, the humanities and social sciences. In so doing, it also takes into account rapid scientific advances from fields such as systems biology, microbiomics, epigenomics or information and communication technologies as well as the hight potential of ''big data'' for public health.
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