State Key Laboratory of Oncology in South China, Collaborative Innovation Center for Cancer Medicine, Guangdong Esophageal Cancer Institute, Sun Yat-sen University Cancer Center, Guangzhou, 510060, People's Republic of China.
J Hematol Oncol. 2022 Dec 8;15(1):173. doi: 10.1186/s13045-022-01391-4.
Epidermal growth factor receptor tyrosine kinase inhibitors (EGFR-TKIs) are the preferential options for advanced non-small cell lung cancer (NSCLC) patients harboring EGFR mutations. Osimertinib is a potent irreversible third-generation EGFR-TKI targeting EGFR mutations but has little effect on wild-type EGFR. In view of its remarkable efficacy and manageable safety, osimertinib was recommended as the standard first-line treatment for advanced or metastatic NSCLC patients with EGFR mutations. However, as the other EGFR-TKIs, osimertinib will inevitably develop acquired resistance, which limits its efficacy on the treatment of EGFR-mutated NSCLC patients. The etiology of triggering osimertinib resistance is complex including EGFR-dependent and EGFR-independent pathways, and different therapeutic strategies for the NSCLC patients with osimertinib resistance have been developed. Herein, we comprehensively summarized the resistance mechanisms of osimertinib and discuss in detail the potential therapeutic strategies for EGFR-mutated NSCLC patients suffering osimertinib resistance for the sake of the improvement of survival and further achievement of precise medicine.
表皮生长因子受体酪氨酸激酶抑制剂(EGFR-TKIs)是携带 EGFR 突变的晚期非小细胞肺癌(NSCLC)患者的首选治疗方案。奥希替尼是一种针对 EGFR 突变的高效、不可逆的第三代 EGFR-TKI,但对野生型 EGFR 几乎没有作用。鉴于其显著的疗效和可控的安全性,奥希替尼被推荐为携带 EGFR 突变的晚期或转移性 NSCLC 患者的标准一线治疗药物。然而,与其他 EGFR-TKIs 一样,奥希替尼不可避免地会产生获得性耐药,这限制了其在治疗 EGFR 突变型 NSCLC 患者方面的疗效。触发奥希替尼耐药的病因复杂,包括 EGFR 依赖性和 EGFR 非依赖性途径,针对奥希替尼耐药的 NSCLC 患者已经开发了不同的治疗策略。在此,我们全面总结了奥希替尼的耐药机制,并详细讨论了针对奥希替尼耐药的 EGFR 突变型 NSCLC 患者的潜在治疗策略,以期改善患者的生存并进一步实现精准医学。