Related Experiment Video
Updated: Apr 22, 2026

Detection of Targetable Alterations in Non-small Cell Lung Cancer using Next-generation Sequencing
Published on: October 10, 2025
Review of the current targeted therapies for non-small-cell lung cancer
Kim-Son H Nguyen1, Joel W Neal1, Heather Wakelee1
1Kim-Son H Nguyen, Joel W Neal, Heather Wakelee, Division of Oncology, Department of Medicine, Stanford University School of Medicine, Stanford, CA 94305, United States.
Abstract:
The last decade has witnessed the development of oncogene-directed targeted therapies that have significantly changed the treatment of non-small-cell lung cancer (NSCLC). In this paper we review the data demonstrating efficacy of gefitinib, erlotinib, and afatinib, which target the epidermal growth factor receptor (EGFR), and crizotinib which targets anaplastic lymphoma kinase (ALK). We discuss the challenge of acquired resistance to these small-molecular tyrosine kinase inhibitors and review promising agents which may overcome resistance, including the EGFR T790M-targeted agents CO-1686 and AZD9291, and the ALK-targeted agents ceritinib (LDK378), AP26113, alectinib (CH/RO5424802), and others. Emerging therapies directed against other driver oncogenes in NSCLC including ROS1, HER2, and BRAF are covered as well. The identification of specific molecular targets in a significant fraction of NSCLC has led to the personalized deployment of many effective targeted therapies, with more to come.
Insights
Targeted therapies have transformed non-small-cell lung cancer (NSCLC) treatment by targeting oncogenes like EGFR and ALK. Researchers are developing new agents to overcome acquired resistance and expand personalized treatment options for NSCLC patients.
Area of Science:
- Oncology
- Molecular Biology
- Pharmacology
Background:
- The last decade has seen significant advancements in targeted therapies for non-small-cell lung cancer (NSCLC).
- These therapies target specific oncogenic drivers, revolutionizing treatment paradigms.
- Epidermal growth factor receptor (EGFR) and anaplastic lymphoma kinase (ALK) are key targets in NSCLC.
Purpose of the Study:
- To review the efficacy of current oncogene-directed targeted therapies for NSCLC.
- To discuss the challenge of acquired resistance to tyrosine kinase inhibitors.
- To highlight emerging agents and targets for overcoming resistance and expanding personalized treatment.
Main Methods:
- Review of clinical trial data and scientific literature.
- Analysis of efficacy data for EGFR and ALK inhibitors.
- Exploration of mechanisms of resistance and novel therapeutic strategies.
Main Results:
- Gefitinib, erlotinib, and afatinib show efficacy against EGFR-mutated NSCLC.
- Crizotinib is effective for ALK-positive NSCLC.
- New agents like CO-1686, AZD9291, ceritinib, and alectinib show promise in overcoming resistance.
Conclusions:
- Personalized medicine, driven by molecular target identification, is transforming NSCLC treatment.
- Ongoing research is crucial for developing strategies to overcome acquired resistance.
- Emerging therapies targeting other oncogenes (ROS1, HER2, BRAF) will further enhance personalized treatment for NSCLC.
More Related Videos
07:59Author Spotlight: Advancements in Molecular Biomarker Testing for Non-Squamous Non-Small Cell Lung Cancer
Published on: September 8, 2023
04:04Endobronchial Ultrasound-guided Intratumoral Injection of Cisplatin for the Treatment of Isolated Mediastinal Recurrence of Lung Cancer
Published on: February 12, 2017
Related Concept Videos
Targeted Cancer Therapies
There are several types of targeted therapies against...
Targeted Cancer Therapies
Combination Therapies and Personalized Medicine
The combination of the drug acetazolamide and sulforaphane is a good example of combination therapy to treat cancer. The cells in the interior of a large tumor often die due to the hypoxic and...
Modified-Release Drug Delivery Systems: Site-Targeted
Tumor Immunotherapy
Cancer Therapies
However, cancer treatments can pose several challenges, as therapies used to kill cancer cells are generally also toxic to normal cells. Moreover, cancer cells mutate rapidly and can develop resistance to chemical agents or radiation therapy. Besides, all types of cancer cells may not respond to the same therapy. Some cancer cells respond to one...