标准化
仿形(计算机编程)
医学
精密医学
医学物理学
主流
计算生物学
数据科学
基因组学
DNA测序
协调
计算机科学
协商一致会议
医学实验室
药品审批
梅德林
专家意见
工程伦理学
临床研究设计
食品药品监督管理局
临床试验
分子诊断学
诊断试验
医学研究
国际标准化
基因检测
出处
期刊:PubMed
[National Institutes of Health]
日期:2026-04-23
卷期号:48 (4): 491-501
标识
DOI:10.3760/cma.j.cn112152-20250722-00356
摘要
Comprehensive genomic profiling (CGP) based on next-generation sequencing (NGS) has emerged as a mainstream approach for clinical diagnosis and treatment with the development of precision oncology. However, as the first stage of NGS testing, probe design has not yet been standardized by a reliable assessment framework. In response to this unmet need, the Cancer Hospital, Chinese Academy of Medical Sciences and Peking Union Medical College, in collaboration with the Tumor Pathology Committee of China Anti-Cancer Association, the National Institutes for Food and Drug Control, and other authoritative institutions, convened clinical experts, pathologists, and representatives from third-party medical laboratories for in-depth discussions on standardization strategies. The expert panel formulated six core technical consensus statements, including the selection of target genes and regions, gene combination strategies, probe performance evaluation, and probe updates, based on a thorough analysis of both international studies and domestic clinical experience. For the design of the probe pool, this consensus methodically suggests a full-process technical specification. It fills a technical gap in tumor NGS probe design by standardizing probe design, establishing a multi-level performance validation system, and dynamically managing probe modifications. Furthermore, it supports the shift of genomic testing from "clinically available" to "clinically reliable" by offering a scientific basis for the National Medical Products Administration's (NMPA) regulatory review of laboratory-developed tests (LDTs) for oncology.
科研通智能强力驱动
Strongly Powered by AbleSci AI