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This is a hypothetical combination of five small molecule tyrosine kinase inhibitors: nintedanib, gefitinib, erlotinib, afatinib, and osimertinib. All five drugs are orally administered and primarily used in the treatment of non-small cell lung cancer (NSCLC), particularly in patients with specific mutations in the epidermal growth factor receptor (EGFR). Nintedanib is a triple angiokinase inhibitor targeting vascular endothelial growth factor receptors (VEGFRs), fibroblast growth factor receptors (FGFRs), and platelet-derived growth factor receptors (PDGFRs). Gefitinib, erlotinib, afatinib, and osimertinb are EGFR tyrosine kinase inhibitors; afatinb irreversibly inhibits EGFR as well as HER2/ErbB2 and HER4/ErbB4. Osimertinb is notable for its activity against T790M resistance mutations in EGFR. This combination has not been described or approved for clinical use as a single regimen; however, individual agents or dual combinations have been studied for advanced NSCLC[1][3][5][6][7].
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