학술논문

Navigating the “No Man's Land” of TKI-Failed EGFR-Mutated Non–Small Cell Lung Cancer (NSCLC): A Review
Document Type
article
Source
Neoplasia. 20(1)
Subject
Biomedical and Clinical Sciences
Clinical Sciences
Oncology and Carcinogenesis
Clinical Trials and Supportive Activities
Cancer
Clinical Research
Lung Cancer
Lung
Good Health and Well Being
Animals
Antineoplastic Agents
Brain Neoplasms
Carcinoma
Non-Small-Cell Lung
Combined Modality Therapy
Disease Progression
ErbB Receptors
Humans
Immunotherapy
Lung Neoplasms
Mutation
Protein Kinase Inhibitors
Recurrence
Oncology & Carcinogenesis
Clinical sciences
Oncology and carcinogenesis
Language
Abstract
As the leading cause of cancer-related mortality, lung cancer is a worldwide health issue that is overwhelmingly caused by smoking. However, a substantial minority (~25%) of patients with non-small cell lung cancer (NSCLC) has never smoked. In these patients, activating mutations of the epidermal growth factor receptor (EGFR) are more likely, which render their tumors susceptible for a finite period to treatment with EGFR tyrosine kinase inhibitors (TKIs) and confer a better prognosis than EGFR wild-type NSCLC. On progression, due to the inevitable insurgence of resistance, TKIs are generally followed by second- or third-line salvage chemotherapy until treatment failure, after which no standard treatment options are available, resulting in a poor prognosis and a high risk of death. With the focus of clinical attention on treatment with TKIs, few studies on optimal salvage therapies, including cytotoxic chemotherapy, after failure of EGFR TKIs have been reported. Despite a paucity of available data, the aim of this review is to summarize the "no-man's land" of TKI-failed EGFR-mutated NSCLC and expand on alternative strategies as well as potential future directions.