Targeted therapy for NSCLC with driver mutations

Gabriele Minuti1, Armida D'Incecco, Federico Cappuzzo

  • 1Medical Oncology Department, Civil Hospital of Livorno, Istituto Toscano Tumori , Viale Alfieri 36, 57100, Livorno , Italy +39 0586 223189 ; +39 0586 223457 ; f.cappuzzo@gmail.com.

Abstract

Insights

Molecular characterization of non-small cell lung cancer (NSCLC) reveals new oncogenes. Targeting these genetic alterations improves treatment strategies and patient outcomes in lung cancer.

Area of Science:

  • Oncology
  • Genetics
  • Molecular Biology

Background:

  • Activating mutations in EGFR and ALK rearrangements are key in non-small cell lung cancer (NSCLC).
  • Numerous genetic aberrations (ROS1, RET, MET, HER2, BRAF, KRAS) are identified, primarily in adenocarcinoma.
  • Emerging oncogenic drivers (DDR2, FGFR1, PI3KCA) are characterized in squamous cell lung carcinoma (SCC).

Purpose of the Study:

  • To review the expanding landscape of targetable oncogenes in NSCLC.
  • To summarize genetic alterations and their therapeutic relevance in lung cancer subtypes.
  • To highlight the evolving role of molecular characterization in NSCLC treatment.

Main Methods:

  • Systematic literature review using PubMed.
  • Analysis of published data on NSCLC genomic alterations.
  • Collection of data on identification techniques, prevalence, tumorigenesis role, and targeted agents.

Main Results:

  • EGFR mutations and ALK rearrangements exemplify therapeutic targets in NSCLC.
  • Various genetic aberrations have prognostic and predictive roles, particularly in adenocarcinoma.
  • New oncogenic drivers are identified in SCC, with targeted agents under evaluation.

Conclusions:

  • Oncogenic products are validated targets for drug development in lung cancer.
  • Increased understanding of molecular pathways is transforming NSCLC treatment strategies.
  • Targeted therapies improve disease control, prolong survival, and enhance quality of life for NSCLC patients.

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