KRAS inhibition in non-small cell lung cancer: Past failures, new findings and upcoming challenges

Eur J Cancer. 2020 Sep:137:57-68. doi: 10.1016/j.ejca.2020.06.023. Epub 2020 Jul 31.

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.

Keywords: AMG510; G12C; KRAS; Lung cancer; Target therapy.

Publication types

  • Review

MeSH terms

  • Carcinoma, Non-Small-Cell Lung / drug therapy*
  • Carcinoma, Non-Small-Cell Lung / pathology
  • Humans
  • Lung Neoplasms / drug therapy*
  • Lung Neoplasms / pathology
  • Molecular Structure
  • Precision Medicine
  • Proto-Oncogene Proteins p21(ras) / antagonists & inhibitors*

Substances

  • Proto-Oncogene Proteins p21(ras)