| Literature DB >> 32745965 |
Francesco Passiglia1, Umberto Malapelle2, Marzia Del Re3, Luisella Righi4, Fabio Pagni5, Daniela Furlan6, Romano Danesi7, Giancarlo Troncone8, Silvia Novello9.
Abstract
Despite the high prevalence of Kirsten rat sarcoma (KRAS) mutations in non-small cell lung cancer (NSCLC), for a long time it has been defined as an 'undruggable target', with precision medicine not considered as an adequate approach to treat this subgroup of patients. After several years of efforts, preliminary data from early clinical trials have recently demonstrated that direct pharmacological inhibition of KRAS p.G12C mutation is possible, emerging as an effective targeted treatment for about 10-12% of patients with advanced NSCLC, with potential relevant impact on their long-term survival and quality of life. This review reports the current status of KRAS mutations detection in the Italian real-word scenario, summarises the biological basis of KRAS inhibition in NSCLC and provides an updated overview of therapeutic strategies, discussing the potential reasons for past failures and analysing the upcoming challenges related to the advent of new targeted agents in clinical practice.Entities:
Keywords: AMG510; G12C; KRAS; Lung cancer; Target therapy
Mesh:
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Year: 2020 PMID: 32745965 DOI: 10.1016/j.ejca.2020.06.023
Source DB: PubMed Journal: Eur J Cancer ISSN: 0959-8049 Impact factor: 9.162