| Literature DB >> 33333743 |
Chiara Lazzari1, Alessandra Bulotta1, Maria Giulia Cangi2, Gabriele Bucci3, Lorenza Pecciarini2, Silvia Bonfiglio3, Vincenza Lorusso1, Stefania Ippati1, Gianluigi Arrigoni2, Greta Grassini2, Claudio Doglioni2, Vanesa Gregorc1.
Abstract
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.Entities:
Keywords: molecular tumor board; next-generation sequencing; non-small cell lung cancer
Year: 2020 PMID: 33333743 DOI: 10.3390/diagnostics10121092
Source DB: PubMed Journal: Diagnostics (Basel) ISSN: 2075-4418