“…EGFR mutations represent the most common type of driver gene mutation in NSCLC, with an incidence of approximately 30–40% [ 49 , 50 ]. Numerous phase II or III clinical trials have validated the efficacy of EGFR-TKIs, demonstrating that targeted therapy considerably ameliorates the prognosis of patients with advanced NSCLC harboring EGFR mutations, compared to chemotherapy [ 38 , [51] , [52] , [53] , [54] ]. The findings also indicate that EGFR-TKIs prolong OS in the most patients, irrespective of the metastasis sites [ 38 , [51] , [52] , [53] , [54] ].…”