Lazzari Chiara, Bulotta Alessandra, Cangi Maria Giulia, Bucci Gabriele, Pecciarini Lorenza, Bonfiglio Silvia, Lorusso Vincenza, Ippati Stefania, Arrigoni Gianluigi, Grassini Greta, Doglioni Claudio, Gregorc Vanesa
Department of Oncology, IRCCS San Raffaele, 20132 Milan, Italy.
Department of Pathology, IRCCS San Raffaele, 20132 Milan, Italy.
Diagnostics (Basel). 2020 Dec 15;10(12):1092. doi: 10.3390/diagnostics10121092.
Lung cancer remains the first cause of cancer-related deaths worldwide. Thanks to the improvement in the knowledge of the biology of non-small cell lung cancer (NSCLC), patients' survival has significantly improved. A growing number of targetable molecular alterations have been identified. Next-generation sequencing (NGS) has become one of the methodologies entered in clinical practice and was recently recommended by the European society for medical oncology (ESMO) to perform a comprehensive molecular characterization in patients with cancer. The current review provides an overview of the clinical trials that have explored the impact of NGS in patients with cancer, its limits, and advantages.
肺癌仍然是全球癌症相关死亡的首要原因。得益于对非小细胞肺癌(NSCLC)生物学认识的提高,患者的生存率有了显著改善。越来越多可靶向的分子改变已被识别。二代测序(NGS)已成为进入临床实践的方法之一,最近欧洲医学肿瘤学会(ESMO)推荐其对癌症患者进行全面的分子特征分析。本综述概述了探索NGS对癌症患者影响的临床试验、其局限性及优势。