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Updated: May 7, 2026

Ultra-Fast Amplicon-Based Next-Generation Sequencing in Non-Squamous Non-Small Cell Lung Cancer
Published on: September 8, 2023
Advances towards the design and development of personalized non-small-cell lung cancer drug therapy
Sabrina Vari1, Sara Pilotto, Marcello Maugeri-Saccà
1Regina Elena National Cancer Institute, Division of Medical Oncology A , Via Elio Chianesi 53, 00144, Rome , Italy +39 06 52666919 ; +39 06 52665637 ; michelemilella@hotmail.com ; milella@ifo.it.
Introduction:
Non-small-cell lung cancer (NSCLC) subtypes are driven by specific genetic aberrations. For reasons such as this, there is a call for treatment personalization. The ability to instigate NSCLC fragmentation poses new methodological problems, and new 'driver' molecular aberrations are being discovered at an unprecedented pace.
Areas Covered:
This article describes the clinical development of epidermal growth factor-tyrosine kinase inhibitors (EGFR-TKIs) and crizotinib for EGFR-mutant and anaplastic lymphoma kinase (ALK)-rearranged NSCLC. Further, the authors briefly describe the emerging molecular targets in NSCLC, in terms of both rationale for therapeutic targeting and strategies, for clinical development.
Expert Opinion:
Target identification and validation in NSCLC still requires considerable effort, as not all of the molecular alterations are clear 'drivers' nor can they be efficiently targeted with available drugs. However, 50% of the NSCLC cases are without clear-defined molecular aberrations. Clinical trial methodology will need to develop novel paradigms for targeted drug development, aiming at the validation of an ideal 'biology-to-trial' approach. Despite significant challenges, a truly 'personalized' approach to NSCLC therapy appears to be within our reach.
Insights
Personalized treatment for non-small-cell lung cancer (NSCLC) is advancing with targeted therapies like EGFR-TKIs and crizotinib. Further research is needed to identify and validate new molecular targets for improved NSCLC patient outcomes.
Area of Science:
- Oncology
- Molecular Biology
- Genetics
Background:
- Non-small-cell lung cancer (NSCLC) subtypes are driven by specific genetic aberrations, necessitating personalized treatment approaches.
- The discovery of novel molecular aberrations in NSCLC is accelerating, presenting both opportunities and challenges for targeted therapy development.
Purpose of the Study:
- To review the clinical development of epidermal growth factor-tyrosine kinase inhibitors (EGFR-TKIs) and crizotinib for EGFR-mutant and ALK-rearranged NSCLC.
- To discuss emerging molecular targets in NSCLC, including the rationale for targeting and clinical development strategies.
Main Methods:
- Review of clinical development of EGFR-TKIs and crizotinib.
- Discussion of emerging molecular targets and therapeutic strategies in NSCLC.
Main Results:
- EGFR-TKIs and crizotinib represent successful targeted therapies for specific NSCLC molecular subtypes.
- Several emerging molecular targets are under investigation for NSCLC treatment.
Conclusions:
- Target identification and validation remain critical challenges in NSCLC, with approximately 50% of cases lacking clear molecular aberrations.
- Novel clinical trial methodologies and a 'biology-to-trial' approach are essential for advancing personalized NSCLC therapy.
- Despite challenges, a personalized approach to NSCLC treatment is increasingly attainable.
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