| Literature DB >> 33588147 |
Umberto Malapelle1, Francesco Passiglia2, Chiara Cremolini3, Maria Lucia Reale2, Francesco Pepe1, Pasquale Pisapia1, Antonio Avallone4, Diego Cortinovis5, Alfonso De Stefano4, Matteo Fassan6, Gabriella Fontanini7, Domenico Galetta8, Calogero Lauricella9, Angela Listì2, Fotios Loupakis10, Fabio Pagni11, Filippo Pietrantonio12, Sara Pilotto13, Luisella Righi2, Andrea Sartore Bianchi14, Hector Soto Parra15, Marcello Tiseo16, Michela Verzè16, Giancarlo Troncone17, Silvia Novello2.
Abstract
Rat sarcoma (RAS) oncogenes have intensively been investigated during the last decades. Taking into account all human tumours, Kirsten Rat Sarcoma Viral Oncogene Homolog (KRAS) gene is the most frequently mutated (about 22%) among the three isoforms, followed by Neuroblastoma RAS Viral Oncogene Homolog (NRAS) (8%) and Harvey Rat Sarcoma Viral Oncogene Homolog (HRAS) (3%). In the last years, careful attention has been paid on KRAS and NRAS gene mutations in non-small-cell lung cancer (NSCLC) and colorectal cancer (CRC) patients because of their prognostic and predictive roles. In particular, a large body of literature data has been generated investigating clinical outcomes of targeted treatments in NSCLC and CRC KRAS- and NRAS-mutated patients. The latest evidences are here reviewed, providing also an overview of the real-world RAS mutation testing practice across different Italian laboratories. On this basis, we propose a knowledge-based system, www.rasatlas.com, to support the healthcare personnel in the management of patients featuring RAS gene mutations in the landscape of precision oncology.Entities:
Keywords: CRC; KRAS; NGS; NRAS; NSCLC
Year: 2021 PMID: 33588147 DOI: 10.1016/j.ejca.2021.01.015
Source DB: PubMed Journal: Eur J Cancer ISSN: 0959-8049 Impact factor: 9.162