Frontiers in Oncology (Dec 2021)

The Renaissance of KRAS Targeting in Advanced Non-Small-Cell Lung Cancer: New Opportunities Following Old Failures

  • Miriam Grazia Ferrara,
  • Miriam Grazia Ferrara,
  • Alessio Stefani,
  • Alessio Stefani,
  • Sara Pilotto,
  • Carmine Carbone,
  • Emanuele Vita,
  • Emanuele Vita,
  • Mariantonietta Di Salvatore,
  • Ettore D’Argento,
  • Ileana Sparagna,
  • Ileana Sparagna,
  • Federico Monaca,
  • Federico Monaca,
  • Giustina Valente,
  • Giustina Valente,
  • Antonio Vitale,
  • Antonio Vitale,
  • Geny Piro,
  • Lorenzo Belluomini,
  • Michele Milella,
  • Giampaolo Tortora,
  • Giampaolo Tortora,
  • Emilio Bria,
  • Emilio Bria

DOI
https://doi.org/10.3389/fonc.2021.792385
Journal volume & issue
Vol. 11

Abstract

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Non-small cell lung cancer (NSCLC) represents the perfect paradigm of ‘precision medicine’ due to its complex intratumoral heterogeneity. It is truly characterized by a range of molecular alterations that can deeply influence the natural history of this disease. Several molecular alterations have been found over time, paving the road to biomarker-driven therapy and radically changing the prognosis of ‘oncogene addicted’ NSCLC patients. Kirsten rat sarcoma (KRAS) mutations are present in up to 30% of NSCLC (especially in adenocarcinoma histotype) and have been identified decades ago. Since its discovery, its molecular characteristics and its marked affinity to a specific substrate have led to define KRAS as an undruggable alteration. Despite that, many attempts have been made to develop drugs capable of targeting KRAS signaling but, until a few years ago, these efforts have been unsuccessful. Comprehensive genomic profiling and wide-spectrum analysis of genetic alterations have only recently allowed to identify different types of KRAS mutations. This tricky step has finally opened new frontiers in the treatment approach of KRAS-mutant patients and might hopefully increase their prognosis and quality of life. In this review, we aim to highlight the most interesting aspects of (epi)genetic KRAS features, hoping to light the way to the state of art of targeting KRAS in NSCLC.

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