Amivantamab通过EGFR/MET表达依赖性机制在非小细胞肺癌中恢复抗肿瘤免疫

Introduction: Epidermal growth factor receptor (EGFR) mutations are one of the most common oncogenic drivers in non-small cell lung cancer (NSCLC). Although EGFR tyrosine kinase inhibitors (EGFR-TKIs) have demonstrated clinical benefits, acquired resistance still limits the long-term efficacy, with activation of MNNG HOS Transforming (MET) signaling serving as a representative bypass mechanism. Recently, amivantamab, a bispecific antibody against EGFR and MET, has shown clinical efficacy. However, its immunological role in human tumors has not been directly investigated. Methods: We analyzed 40 surgically resected fresh NSCLC samples to evaluate EGFR/MET expression and their correlation with immune suppression. Tumor-infiltrating lymphocytes (TILs) were evaluated by flow cytometry and immunohistochemistry. To assess the immunomodulatory effects of amivantamab, tumor digests including viable TILs were cultured ex vivo under conditions with or without amivantamab. Results: EGFR mutations and elevated EGFR protein expression showed a tendency for reduced infiltration of CD8⁺ T cells and dendritic cells (DCs). Ex vivo exposure to amivantamab enhanced CD8⁺ T-cell effector functions and DC maturation in TILs, particularly in tumors with high EGFR/MET expression, independent of EGFR mutation status. Conclusion: This study provides the first direct evidence using fresh human NSCLC samples that amivantamab can restore antitumor immunity through CD8⁺ T-cell activation and DC maturation. Expression levels of EGFR and MET may serve as predictive biomarkers for amivantamab monotherapy as well as for amivantamab-based combination immunotherapies.