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Updated: May 9, 2026

Ultra-Fast Amplicon-Based Next-Generation Sequencing in Non-Squamous Non-Small Cell Lung Cancer
Published on: September 8, 2023
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.
Introduction:
Activating mutations of the epidermal growth factor receptor (EGFR) gene and rearrangement of anaplastic lymphoma kinase (ALK) gene best illustrate the therapeutic relevance of molecular characterization in non-small cell lung cancer (NSCLC) patients. Several genetic aberrations with a potential prognostic or predictive role have been identified, mainly in adenocarcinoma subtype, including ROS1, RET, MET, HER2, BRAF and KRAS. More recently oncogenic drivers, such as DDR2, FGFR1 and PI3KCA, have been characterized in squamous cell lung carcinoma (SCC) and target agents are currently under evaluation. The aim of this review is to summarize the growing scenario of new targetable oncogenes in NSCLC.
Areas Covered:
For this review article all published data on NSCLC genomic alterations, including the techniques employed for oncogenic drivers identification, the prevalence of each one in lung cancer subtypes, the preclinical data corroborating their role in tumorigenesis and the potential biological tailored agents tested and under evaluation were collected and analyzed using PubMed.
Expert Opinion:
Oncogenic products represent reliable targets for drug therapy and the expanding knowledge of molecular pathways involved in lung tumorigenesis is resulting in a dramatic change of treatment strategies leading to an improvement in disease and symptom control, extending life duration and improving quality of life.
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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