神经纤维瘤病和雪旺细胞瘤临床试验中生物标志物分析用生物样本采集和注释的推荐意见。
Recommendations for the collection and annotation of biosamples for analysis of biomarkers in neurofibromatosis and schwannomatosis clinical trials.
机构信息
Pediatric Oncology Branch, National Cancer Institute, Bethesda, MD, USA.
Division of Hematology/Oncology/Stem Cell Transplant, Department of Pediatrics, Herman B Wells Center for Pediatric Research, School of Medicine, Indiana University, Indianapolis, IN, USA.
出版信息
Clin Trials. 2024 Feb;21(1):40-50. doi: 10.1177/17407745231203330. Epub 2023 Oct 31.
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.
简介
神经纤维瘤病 1 型和神经鞘瘤病的特点是终生存在发病风险和危及生命的并发症。然而,迄今为止,该患者群体仍缺乏诊断和预测生物标志物。在神经纤维瘤病 1 型/神经鞘瘤病临床试验中纳入生物标志物发现相关因素,可以研究发病率较低的疾病。采用通用数据模型将进一步增强生物标志物的发现能力,从而有效整合来自多个研究的数据。
方法
神经纤维瘤病和神经鞘瘤病生物标志物工作组回顾了神经纤维瘤病 1 型和神经鞘瘤病生物标志物研究中新兴趋势的已发表数据,并在一系列共识会议中制定了相关建议。
结果
液体活检已成为神经纤维瘤病 1 型/神经鞘瘤病生物标志物发现和验证的一种很有前途的检测方法。此外,我们还回顾了临床试验中一系列生物标志物、神经纤维瘤病 1 型/神经鞘瘤病特定数据注释以及数据集成通用数据模型的建议。
结论
这些神经纤维瘤病和神经鞘瘤病反应评估共识指南旨在为神经纤维瘤病 1 型/神经鞘瘤病临床试验、数据和样本注释中纳入生物标志物研究提供最佳实践,并为试验之间的数据协调和整合奠定框架。