Recommendations for the collection and annotation of biosamples for analysis of biomarkers in neurofibromatosis and schwannomatosis clinical trials.

IF 2.2 3区 医学 Q3 MEDICINE, RESEARCH & EXPERIMENTAL
Clinical Trials Pub Date : 2024-02-01 Epub Date: 2023-10-31 DOI:10.1177/17407745231203330
R Taylor Sundby, Steven D Rhodes, Edina Komlodi-Pasztor, Herb Sarnoff, Vito Grasso, Meena Upadhyaya, AeRang Kim, D Gareth Evans, Jaishri O Blakeley, C Oliver Hanemann, Chetan Bettegowda
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引用次数: 0

Abstract

Introduction: Neurofibromatosis 1 and schwannomatosis are characterized by potential lifelong morbidity and life-threatening complications. To date, however, diagnostic and predictive biomarkers are an unmet need in this patient population. The inclusion of biomarker discovery correlatives in neurofibromatosis 1/schwannomatosis clinical trials enables study of low-incidence disease. The implementation of a common data model would further enhance biomarker discovery by enabling effective concatenation of data from multiple studies.

Methods: The Response Evaluation in Neurofibromatosis and Schwannomatosis biomarker working group reviewed published data on emerging trends in neurofibromatosis 1 and schwannomatosis biomarker research and developed recommendations in a series of consensus meetings.

Results: Liquid biopsy has emerged as a promising assay for neurofibromatosis 1/schwannomatosis biomarker discovery and validation. In addition, we review recommendations for a range of biomarkers in clinical trials, neurofibromatosis 1/schwannomatosis-specific data annotations, and common data models for data integration.

Conclusion: These Response Evaluation in Neurofibromatosis and Schwannomatosis consensus guidelines are intended to provide best practices for the inclusion of biomarker studies in neurofibromatosis 1/schwannomatosis clinical trials, data, and sample annotation and to lay a framework for data harmonization and concatenation between trials.

神经纤维瘤病和神经鞘瘤病临床试验中生物标志物分析生物样本的收集和注释建议。
引言:神经纤维瘤病1和神经鞘瘤病的特点是潜在的终身发病率和危及生命的并发症。然而,到目前为止,诊断和预测生物标志物在这一患者群体中尚未得到满足。在神经纤维瘤病1/神经鞘瘤病临床试验中纳入生物标志物发现相关性,使低发病率疾病的研究成为可能。通用数据模型的实施将通过实现多个研究数据的有效串联,进一步增强生物标志物的发现。方法:神经纤维瘤病和神经鞘瘤病生物标志物的反应评估工作组审查了已发表的关于神经纤维瘤瘤病1和神经鞘膜瘤病生物标记物研究新趋势的数据,并在一系列共识会议上提出了建议。结果:液体活检已成为发现和验证神经纤维瘤病1/神经鞘瘤病生物标志物的一种有前途的方法。此外,我们还回顾了临床试验中一系列生物标志物的建议,神经纤维瘤病1/神经鞘瘤病特异性数据注释,以及用于数据整合的常见数据模型。结论:这些神经纤维瘤病和神经鞘瘤病的反应评估共识指南旨在为将生物标志物研究纳入神经纤维瘤症1/神经鞘瘤症临床试验、数据和样本注释提供最佳实践,并为试验之间的数据协调和连接奠定框架。
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来源期刊
Clinical Trials
Clinical Trials 医学-医学:研究与实验
CiteScore
4.10
自引率
3.70%
发文量
82
审稿时长
6-12 weeks
期刊介绍: Clinical Trials is dedicated to advancing knowledge on the design and conduct of clinical trials related research methodologies. Covering the design, conduct, analysis, synthesis and evaluation of key methodologies, the journal remains on the cusp of the latest topics, including ethics, regulation and policy impact.
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