Related Experiment Video
Updated: Feb 5, 2026

Detection of Targetable Alterations in Non-small Cell Lung Cancer using Next-generation Sequencing
Published on: October 10, 2025
[Advances in Double Mutations of EGFR and ALK Gene in Non-small Cell Lung Cancer]
1Department of Medical Oncology, Tianjin Medical University General Hospital, Tianjin 300052, China.
Abstract:
Molecular target therapy is one of the most popular field of non-small cell lung cancer (NSCLC) treatmnet. Epidermal growth factor receptor (EGFR) mutation and anaplastic lymphoma kinase (ALK) rearragement are the most important two oncogenic drivers in NSCLC, early studies suggested that EGFR mutations and ALK rearrangements are mutually exclusive, but isolated cases or small sample research with concomitant EGFR and ALK alterations have been constantly reported. The co-occurrence of EGFR mutations and anaplastic lymphoma kinase (ALK) rearrangements constitutes a rare molecular, the frequency of EGFR/ALK co-alterations was about 1%, however, little has been known about clinicopathologic feature and treatment. This review summarized published case report, EGFR and ALK alterations are common in female, Asian origin, never smoker, IV stage, and denocarcinomas. First-line treatment can choose EGFR or ALK tyrosine kinase inhibitors (TKIs). However, studies about the origin and resistance mechanism in EGFR/ALK co-alterations are little, require more experimental and clinical research. .
Insights
This review explores rare co-occurring Epidermal Growth Factor Receptor (EGFR) mutations and Anaplastic Lymphoma Kinase (ALK) rearrangements in non-small cell lung cancer (NSCLC). It highlights common patient features and treatment options, emphasizing the need for further research.
Area of Science:
- Oncology
- Molecular Biology
- Genetics
Background:
- Molecular targeted therapy is crucial for non-small cell lung cancer (NSCLC) treatment.
- Epidermal Growth Factor Receptor (EGFR) mutations and Anaplastic Lymphoma Kinase (ALK) rearrangements are key oncogenic drivers in NSCLC.
- While often considered mutually exclusive, concomitant EGFR and ALK alterations occur rarely (approx. 1%) in NSCLC patients.
Purpose of the Study:
- To review the clinicopathologic features and treatment strategies for NSCLC patients with co-occurring EGFR mutations and ALK rearrangements.
- To identify common characteristics of patients with this rare molecular profile.
- To highlight knowledge gaps regarding the origin and resistance mechanisms of these co-alterations.
Main Methods:
- Systematic review of published case reports and small sample studies.
- Analysis of clinicopathologic data and treatment outcomes for NSCLC with EGFR/ALK co-alterations.
Main Results:
- EGFR/ALK co-alterations are frequently observed in female, Asian, never-smoker patients with Stage IV adenocarcinoma.
- First-line treatment options include EGFR or ALK tyrosine kinase inhibitors (TKIs).
Conclusions:
- Co-occurring EGFR mutations and ALK rearrangements represent a rare but distinct molecular subtype of NSCLC.
- Further experimental and clinical research is essential to understand the origins and resistance mechanisms in these patients.
More Related Videos
Related Concept Videos
Mutation, Gene Flow, and Genetic Drift
Cancers Originate from Somatic Mutations in a Single Cell
Mutations
Mutations
Chromosomal Alterations Are Large-Scale Mutations
While point mutations are changes in a single nucleotide in...
Fixing Double-strand Breaks
Viral Mutations

