设计和实施个性化医学研究的所有阶段的PERMIT指南
Paula Garcia1, Rita Banzi2, Vibeke Fosse3
1European Clinical Research Infrastructure Network (ECRIN), Paris, France. garcialobato.paula@gmail.com.
Scientific reports
|November 13, 2024
概括
PERMIT项目为个性化医学 (PM) 研究制定了方法建议. 这些指导方针提高了证据的可靠性,并通过从数据收集到临床试验设计的PM研究进行标准化来改善患者护理.
科学领域:
- 生物医学研究生物医学研究
- 翻译科学 翻译科学
- 医疗信息学 医疗信息学
背景情况:
- 个性化医学 (PM) 研究需要复杂,跨学科的方法.
- 确保在PM研究中提供可靠和可重复的证据,需要严格的方法.
研究的目的:
- 为整个PM研究管道制定全面的方法建议.
- 提高PM研究研究的质量和可重复性.
主要方法:
- 合作开发涉及利益相关者和专门的工作组.
- 范围审查用于映射现有的PM研究方法并确定差距.
- 专家主导的工作会议,研讨会,以及为最终确定建议建立共识.
主要成果:
- 定义了涵盖PM研究所有阶段的建议,从数据收集到临床试验设计.
- 指导包括患者和OMIC数据处理,样本大小计算,分层,机器学习,临床前模型和临床试验设计.
- 建议旨在提高PM研究中产生的证据的质量和稳定性.
结论:
- 这些建议的传播和实施可以显著提高PM研究质量.
- 加强证据的稳定性最终将导致改善患者护理.
- 标准化的方法对于推进个性化医疗领域至关重要.
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