Developing Consensus for a More Provider-Friendly Next Generation Sequencing Molecular Biomarker Report: A Joint Consensus Recommendation of the Association for Molecular Pathology and College of American Pathologists.

IF 3.4 3区 医学 Q1 PATHOLOGY
Jane Gibson, Hanadi El Achi, Dana Altenburger, Noah Brown, Amy S Clark, Joshua Coleman, Rajyasree Emmadi, Amber M Fussell, Meera Hameed, Danielle Jordan, Jennifer Laudadio, Anthony Provenzano, Robyn L Temple-Smolkin, Christopher G Suciu
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引用次数: 0

Abstract

Despite the increasing availability of next-generation sequencing (NGS) gene panel analysis for cancers, published reports suggest under-utilization of testing, citing the shortage of credentialed professionals available to assist with the interpretation of test results among the key barriers. Obtaining a multidisciplinary consensus regarding a shared best practice NGS molecular biomarker reporting section template may facilitate introduction and/or increased testing for institutions that adopt similar report structures by improving report effectiveness and efficiency for both healthcare providers and laboratory professionals, leading to improved patient care. To address this challenge, the Association for Molecular Pathology convened a multidisciplinary collaborative expert working group to identify and utilize best practices from current reporting guidelines and approaches to develop an NGS biomarker report template to optimally present complex molecular profiling information for efficient use by oncologists and other healthcare providers. Seventeen non-small cell lung cancer NGS biomarker reports from public, private, and academic laboratories were reviewed and specific components (e.g., report length, color use, formatting, presentation order of information, specific information included or omitted, tables, figures) assessed for their ability to be considered "provider-friendly." Based on this review, public and stakeholder input, available literature, and cumulative professional experience of the working group members, a guideline-concordant reporting template was developed based on expert opinion consensus and made freely available online with planned implementation assessment.

为一个对提供者更友好的下一代测序分子生物标志物报告达成共识:分子病理学协会和美国病理学家学院的联合共识建议。
尽管用于癌症的下一代测序(NGS)基因小组分析的可用性越来越高,但已发表的报告表明,检测的利用不足,理由是缺乏合格的专业人员来协助解释检测结果,这是主要障碍之一。获得关于共享的最佳实践NGS分子生物标志物报告部分模板的多学科共识,可以通过提高医疗保健提供者和实验室专业人员的报告有效性和效率,促进采用类似报告结构的机构引入和/或增加测试,从而改善患者护理。为了应对这一挑战,分子病理学协会召集了一个多学科合作专家工作组,从当前的报告指南和方法中确定和利用最佳实践,开发NGS生物标志物报告模板,以最佳方式呈现复杂的分子分析信息,供肿瘤学家和其他医疗保健提供者有效使用。我们审查了来自公共、私人和学术实验室的17份非小细胞肺癌NGS生物标志物报告,并评估了特定成分(例如,报告长度、颜色使用、格式、信息的呈现顺序、包括或省略的特定信息、表格、图表)是否能够被认为是“提供者友好”的。基于这一审查、公众和利益相关方的意见、现有文献以及工作组成员的累积专业经验,在专家意见共识的基础上开发了一个与指南一致的报告模板,并在网上免费提供计划实施评估。
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来源期刊
CiteScore
8.10
自引率
2.40%
发文量
143
审稿时长
43 days
期刊介绍: The Journal of Molecular Diagnostics, the official publication of the Association for Molecular Pathology (AMP), co-owned by the American Society for Investigative Pathology (ASIP), seeks to publish high quality original papers on scientific advances in the translation and validation of molecular discoveries in medicine into the clinical diagnostic setting, and the description and application of technological advances in the field of molecular diagnostic medicine. The editors welcome for review articles that contain: novel discoveries or clinicopathologic correlations including studies in oncology, infectious diseases, inherited diseases, predisposition to disease, clinical informatics, or the description of polymorphisms linked to disease states or normal variations; the application of diagnostic methodologies in clinical trials; or the development of new or improved molecular methods which may be applied to diagnosis or monitoring of disease or disease predisposition.
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