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[Application of Immune Checkpoint Inhibitors in EGFR Mutant Advanced Non-small Cell Lung Cancer]
Yujun Zheng1, Wei Jiang1, Jing Li1
1The Friendship Hospital of Dalian, Dalian 116001, China.
Abstract:
In recent years, immune checkpoint inhibitors (ICIs) have greatly improved the survival rate of non-small cell lung cancer (NSCLC) patients without driver mutation. Compared with wild-type tumors, tumors with epidermal growth factor receptor (EGFR) mutations have greater heterogeneity in immune microenvironment characteristics such as programmed cell death ligand 1 (PD-L1) and tumor mutational burden (TMB). Whether ICIs is suitable for NSCLC patients with EGFR mutation has been controversial. Clinical studies have shown that immunomonotherapy has no significant effect on patients with EGFR mutant NSCLC. ICIs combined with chemotherapy and antiangiogenic drugs show good survival benefits. This paper overviews the clinical research and related mechanism of ICIs single drug or combination therapy inadvanced NSCLC patients with EGFR mutation. .
Insights
Immune checkpoint inhibitors (ICIs) show limited efficacy as monotherapy for non-small cell lung cancer (NSCLC) with EGFR mutations. Combination therapies, however, offer survival benefits for these patients.
Area of Science:
- Oncology
- Immunotherapy
- Genetics
Background:
- Immune checkpoint inhibitors (ICIs) have improved survival in non-small cell lung cancer (NSCLC) without driver mutations.
- NSCLC tumors with epidermal growth factor receptor (EGFR) mutations exhibit heterogeneous immune microenvironments (e.g., PD-L1, TMB).
- The efficacy of ICIs in EGFR-mutated NSCLC remains controversial, with monotherapy showing limited benefit.
Purpose of the Study:
- To review clinical research on ICIs in advanced NSCLC patients with EGFR mutations.
- To explore the mechanisms underlying ICI efficacy in this patient subgroup.
- To evaluate both single-agent and combination ICI therapies.
Main Methods:
- Literature review of clinical studies and mechanistic research.
- Analysis of data regarding ICI monotherapy versus combination therapy.
- Focus on advanced NSCLC patients with documented EGFR mutations.
Main Results:
- ICI monotherapy has demonstrated no significant effect in EGFR-mutant NSCLC.
- Combination therapies (ICIs with chemotherapy and antiangiogenic drugs) show promising survival benefits.
- Heterogeneity in immune markers like PD-L1 and TMB exists in EGFR-mutant tumors.
Conclusions:
- ICI monotherapy is not recommended for EGFR-mutant NSCLC.
- Combination strategies involving ICIs are effective and improve survival in this population.
- Further research into mechanisms is needed to optimize treatment for EGFR-mutant NSCLC.
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