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Is the game over for PD-1 inhibitors in EGFR mutant non-small cell lung cancer?
Author(s) -
Maria A. Velez,
Timothy F. Burns
Publication year - 2019
Publication title -
translational lung cancer research
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.474
H-Index - 41
eISSN - 2226-4477
pISSN - 2218-6751
DOI - 10.21037/tlcr.2019.04.09
Subject(s) - pembrolizumab , medicine , lung cancer , epidermal growth factor receptor , cancer research , tyrosine kinase , pd l1 , mutant , egfr inhibitors , mutation , cancer , oncology , receptor , immunotherapy , biology , gene , genetics
The immune checkpoint inhibitor pembrolizumab, has been shown to be efficacious and to have significant and durable antitumor activity in a subset of patients with advanced non-small cell lung cancer (NSCLC). Most notably in NSCLC with high expression of the programmed death ligand-1 (PD-L1). Similarly, there is abundant data to support the use of epithelial growth factor receptor (EGFR) tyrosine kinase inhibitors (TKIs) as first-line therapy in patients whose tumors harbor EGFR mutations (1).

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