Related Experiment Video
Updated: Mar 7, 2026

Characterize Disease-related Mutants of RAF Family Kinases by Using a Set of Practical and Feasible Methods
Published on: July 17, 2019
Therapeutic approach to treating patients with BRAF-mutant lung cancer: latest evidence and clinical implications
Adrianus J de Langen1, Egbert F Smit2
1Department of Pulmonary Diseases, VU University Medical Center, De Boelelaan 1117, 1007 MB Amsterdam, The Netherlands.
Abstract:
Lung adenocarcinoma is known for its high rate of somatic mutations and genomic rearrangements. The identification of epidermal growth factor receptor (EGFR) mutations and anaplastic lymphoma kinase (ALK) rearrangements that sensitize tumors to specific drugs has changed the therapeutic approach and prognosis in these molecularly-defined subgroups. Several other key genetic alterations have been identified, of which BRAF mutations are found in 4% of non-small cell lung cancer (NSCLC) cases. Targeted drugs against BRAF and downstream MEK were recently approved for the treatment of BRAF-positive melanoma and have entered clinical evaluation in NSCLC. In this review we discuss the latest evidence on the treatment of BRAF-mutated NSCLC, including tumor biology, targeted treatment with BRAF and MEK inhibitors, therapeutic resistance and strategies to overcome resistance.
Insights
BRAF mutations in lung adenocarcinoma present a targetable pathway. This review covers BRAF-mutated non-small cell lung cancer (NSCLC) treatment, resistance, and overcoming challenges with BRAF and MEK inhibitors.
Area of Science:
- Oncology
- Genomics
- Pharmacology
Background:
- Lung adenocarcinoma exhibits frequent somatic mutations and genomic alterations.
- Epidermal growth factor receptor (EGFR) mutations and anaplastic lymphoma kinase (ALK) rearrangements have guided targeted therapies in NSCLC.
- BRAF mutations occur in approximately 4% of non-small cell lung cancer (NSCLC) cases.
Purpose of the Study:
- To review the latest evidence on treating BRAF-mutated NSCLC.
- To discuss tumor biology, targeted therapies, and resistance mechanisms.
- To explore strategies for overcoming therapeutic resistance in BRAF-mutated NSCLC.
Main Methods:
- Literature review of recent studies on BRAF-mutated NSCLC.
- Analysis of clinical trial data for BRAF and MEK inhibitors.
- Examination of molecular mechanisms of resistance to targeted therapies.
Main Results:
- BRAF and MEK inhibitors show promise in treating BRAF-mutated NSCLC, with approvals in melanoma.
- Understanding tumor biology is crucial for effective targeted treatment.
- Therapeutic resistance is a significant challenge, necessitating further research into overcoming it.
Conclusions:
- Targeted therapy with BRAF and MEK inhibitors represents a promising avenue for BRAF-mutated NSCLC.
- Further investigation into resistance mechanisms and novel therapeutic strategies is essential for improving patient outcomes.
- Personalized medicine approaches based on genetic alterations are transforming NSCLC treatment.
More Related Videos
06:51Utilizing 18F-FDG PET/CT Imaging and Quantitative Histology to Measure Dynamic Changes in the Glucose Metabolism in Mouse Models of Lung Cancer
Published on: July 21, 2018
09:38Establishment and Characterization of Three Afatinib-resistant Lung Adenocarcinoma PC-9 Cell Lines Developed with Increasing Doses of Afatinib
Published on: June 26, 2019
Related Concept Videos
Targeted Cancer Therapies
There are several types of targeted therapies against...
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...
Tumor Immunotherapy