标准化
可读性
多学科方法
肺癌
医学
计算机科学
克拉斯
医学物理学
临床实习
肿瘤科
癌症
内科学
家庭医学
社会学
程序设计语言
结直肠癌
操作系统
社会科学
作者
Umberto Malapelle,Alessandro Delle Donne,Fabio Pagni,Filippo Fraggetta,Elena Guerini Rocco,Giulia Pasello,Giuseppe Perrone,Francesco Pepe,Simona Vatrano,Sandro Pignata,Carmine Pinto,Giancarlo Pruneri,Antonio Russo,Héctor Soto Parrà,S. Vallone,Antonio Marchetti,Giancarlo Troncone,Silvia Novello
标识
DOI:10.1016/j.critrevonc.2023.104217
摘要
Molecular biomarker testing is increasingly becoming standard of care for advanced non-small cell lung cancer (NSCLC). Tissue and liquid biopsy-based next-generation sequencing (NGS) is now highly recommended and has become an integral part of the routine management of advanced NSCLC patients. This highly sensitive approach can simultaneously and efficiently detect multiple biomarkers even in scant samples. However full optimization of NGS in clinical practice requires accurate reporting and interpretation of NGS findings. Indeed, as the number of NSCLC biomarkers continues to grow, clinical reporting of NGS data is becoming increasingly complex. In this scenario, achieving standardization, simplification, and improved readability of NGS reports is key to ensuring timely and appropriate treatment decisions. In an effort to address the complexity and lengthy reporting of NGS mutation results, an Italian group of 14 healthcare professionals involved in NSCLC management convened in 2023 to address the content, structure, and ease-of-use of NGS reporting practices and proposed a standard report template for clinical use This article presents the key discussion points addressed by the Italian working group and describes the essential elements of the report template.
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