影响前列腺癌基因组检测的因素:决定基因组评估(DECIDE)调查的决策、经验和信心的结果。

IF 5.3 2区 医学 Q1 ONCOLOGY
JCO precision oncology Pub Date : 2025-05-01 Epub Date: 2025-05-15 DOI:10.1200/PO-24-00821
Rhonda L Bitting, Christopher McNair, Alexander W Wyatt, Gillian Vandekerkhove, Taehwa Choi, Amy E Leader, Joshua Blanding-Godbolt, Laura Gross, Khaldoun Hamade, Susan Halabi, Veda N Giri
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引用次数: 0

摘要

目的:基因组检测对前列腺癌(PCa)临床管理和遗传性癌评估的临床影响越来越大;然而,在最佳实施和最终用户信心方面仍然存在挑战。决定基因组评估的决策、经验和信心(DECIDE)调查旨在收集PCa医疗保健提供者、研究人员和利益相关者关于基因组测试的效用和理解的信息。方法:于2022年10月至2023年1月进行在线调查,共18道多重回答题。调查领域包括订购和解释生殖系和体细胞基因组测试的自信、测试过程和结果的使用、决策因素和测试障碍。通过评估应答数和百分比来总结数据,并通过描述性统计来呈现结果。结果:122名参与者完成了调查。大多数是医学肿瘤学家(70%)和学术医疗中心(89%)。在了解基因组检测适应症方面(82%的受访者)自信很高,但对结果的解释较低,特别是对循环肿瘤DNA的解释(52%)。在解释致病变异(高置信度65%)、意义不明的变异(47%)和基因组检测的偶然发现(35%)方面,置信度各不相同。常见的检测障碍是难以获得组织(71%)和费用(35%)。检测效用有时因无法获得推荐治疗而受到限制(33%)。大多数受访者(55%)认为,缺乏对卫生保健专业人员的基因组检测教育和培训阻碍了临床转化。结论:从提供者对解释结果的信心到测试和实践障碍,DECIDE调查提供了对基因组测试挑战的关键见解。结果为下一步进一步教育前列腺癌提供者提供信息,并共同改进检测和结果报告,以增强前列腺癌基因组检测的实施。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Factors Affecting Genomic Testing in Prostate Cancer: Results From the Decision-Making, Experience, and Confidence In Determining Genomic Evaluation (DECIDE) Survey.

Purpose: Genomic testing for prostate cancer (PCa) clinical management and hereditary cancer assessment has grown in clinical impact; however, challenges remain regarding optimal implementation and end-user confidence. The Decision-making, Experience, and Confidence In Determining Genomic Evaluation (DECIDE) survey was designed to collect information regarding utility and understanding of genomic testing from PCa health care providers, researchers, and stakeholders.

Methods: The DECIDE survey was administered online from October 2022 to January 2023 with 18 multiple-response questions. Survey domains included self-confidence with ordering and interpreting germline and somatic genomic tests, process of testing and use of results, decision-making factors, and barriers to testing. Data were summarized by evaluating counts and percentages of responses, and the results were presented by descriptive statistics.

Results: One hundred twenty-two participants completed the survey. The majority were medical oncologists (70%) and at academic medical centers (89%). Self-confidence was high in knowing indications for genomic testing (82% respondents) but lower in interpretation of results, especially from circulating tumor DNA (52%). Confidence varied in interpreting pathogenic variants (65% high confidence), variants of unknown significance (47%), and incidental findings from genomic tests (35%). Common barriers to testing were difficulty obtaining tissue (71%) and cost (35%). Testing utility was sometimes limited by inability to obtain the recommended treatment (33%). Most of the respondents (55%) agreed that lack of education and training of health care professionals regarding genomic testing is impeding clinical translation.

Conclusion: The DECIDE survey provided critical insights into challenges with genomic testing, from provider confidence in interpretating results to testing and practice barriers. The results inform next steps to further educate PCa providers and to collectively improve testing and result reporting for enhanced implementation of PCa genomic testing.

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CiteScore
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