Discovery of Potent and Wild-Type-Sparing Fourth-Generation EGFR Inhibitors for Treatment of Osimertinib-Resistance NSCLC

Abstract

Osimertinib resistance is an unmet clinical need for the treatment of non-small cell lung cancer (NSCLC), and the main mechanism is tertiary C797S mutation of epidermal growth factor receptor (EGFR). To date, there is no inhibitor approved for the treatment of Osimertinib-resistant NSCLC. Herein, we reported a series of Osimertinib derivatives as fourth-generation inhibitors which were rationally designed. Top candidate <b>D51</b> potently inhibited the EGFR^{L858R/T790M/C797S} mutant with an IC₅₀ value of 14 nM and suppressed the proliferation of H1975-TM cells with an IC₅₀ value of 14 nM, which show over 500-fold selectivity against wild-type forms. Moreover, <b>D51</b> inhibited the EGFR^{del19/T790M/C797S} mutant and the proliferation of the PC9-TM cell line with IC₅₀ values of 62 and 82 nM. <b>D51</b> also exhibited favorable in vivo druggability, including PK parameters, safety properties, in vivo stability, and antitumor activity.