Immunotherapy in EGFR-mutant non-small cell lung cancer.
1/5 보강
Patients with non-small cell lung cancer (NSCLC) with epidermal growth factor receptor (EGFR).For driver mutations, the use of EGFR tyrosine kinase inhibitors (TKIs) is the standard treatment, but acq
APA
Wang L, Xian X, et al. (2025). Immunotherapy in EGFR-mutant non-small cell lung cancer.. Clinical and experimental medicine, 26(1), 10. https://doi.org/10.1007/s10238-025-01927-1
MLA
Wang L, et al.. "Immunotherapy in EGFR-mutant non-small cell lung cancer.." Clinical and experimental medicine, vol. 26, no. 1, 2025, pp. 10.
PMID
41249684
Abstract
Patients with non-small cell lung cancer (NSCLC) with epidermal growth factor receptor (EGFR).For driver mutations, the use of EGFR tyrosine kinase inhibitors (TKIs) is the standard treatment, but acquired resistance is inevitable. There is currently no standard treatment for first-line TKI-resistant NSCLC patients. In recent years, although immune checkpoint inhibitors (ICIs) have transformed the treatment paradigm for advanced NSCLC without driver gene mutations, the clinical efficacy of these agents in patients with advanced NSCLC harboring EGFR mutations remains limited. Whether ICIs are suitable for patients with EGFR-mutated advanced NSCLC still warrants further investigation.This review summarizes several clinically utilized ICIs, presents clinical evidence regarding the efficacy of immunotherapy in patients with EGFR-mutated advanced NSCLC, and identifies EGFR-mutated subpopulations that may benefit from ICI treatment. On this basis, we explored more effective therapeutic strategies to extend the benefits of immunotherapy to a larger cohort of patients with EGFR-mutated NSCLC.
MeSH Terms
Humans; Carcinoma, Non-Small-Cell Lung; ErbB Receptors; Lung Neoplasms; Mutation; Immunotherapy; Immune Checkpoint Inhibitors; Protein Kinase Inhibitors
같은 제1저자의 인용 많은 논문 (5)
- SLC2A1 tumour-associated macrophages spatially control CD8 T cell function and drive resistance to immunotherapy in non-small-cell lung cancer.
- Dual-stage pulmonary nodule detection in CT scans via cross-layer attention and adaptive multi-scale 3D CNN.
- Self-assembly driven nano-salinomycin for high-efficiency cancer immunotherapy by reticulum stress mediated stemness suppression.
- Predictive prioritization of enhancers associated with pancreatic disease risk.
- DUSP22 dephosphorylates LGALS1 to enhance T cell-driven antitumor immunity.