| Literature DB >> 33392095 |
Leilei Wu1,2, Linping Ke2, Zhenshan Zhang1, Jinming Yu2, Xue Meng2.
Abstract
Epidermal growth factor receptor tyrosine kinase inhibitors (EGFR TKIs) have been first-line therapy in the treatment of non-small cell lung cancer (NSCLC) harboring EGFR sensitive mutations. Progression inevitably happens after 10-14 months of first- or second-generation EGFR TKIs treatment for acquired resistance. Owing to the successful identification of EGFR T790M, third-generation EGFR TKIs such as osimertinib were developed to target such resistance mutation. Nowadays, osimertinib has shown its efficacy both in first-line and second-line after resistance to previous generations of TKI treatment of EGFR-mutant NSCLC. However, drug resistance also emerges on third-generation EGFR TKIs. Multiple mechanisms of acquired resistance have been identified, and some novel strategies were reported to overcome third-generation TKI resistance. Immune checkpoint inhibitors (ICIs) have dramatically changed the prognosis of selected patients. For patients with EGFR-addicted metastatic NSCLC, ICIs have also revealed a potential role. In this review, we will take stock of mechanisms of acquired resistance to third-generation TKIs and discuss current challenges and future perspectives in clinical practice.Entities:
Keywords: EGFR TKI resistance; combination (combined) therapy; immune check inhibitor; mechanisms of resistance; molecular biomarkers; osimertinib; tumor immune environment
Year: 2020 PMID: 33392095 PMCID: PMC7775519 DOI: 10.3389/fonc.2020.602762
Source DB: PubMed Journal: Front Oncol ISSN: 2234-943X Impact factor: 6.244