Lee Arnold
Springer Nature, Private Bag 65901, Mairangi Bay, Auckland 0754, New Zealand.
Drugs. 2025 Jun 23. doi: 10.1007/s40265-025-02184-y.
Limertinib (Aoyixin) is an orally available, third-generation epidermal growth factor receptor (EGFR) tyrosine kinase inhibitor (TKI), which has been developed for the treatment of non-small cell lung cancer (NSCLC). In clinical trials, limertinib demonstrated efficacy in patients who are positive for the T790M gatekeeper mutation. Limertinib received its first approval for the treatment of adults with locally advanced or metastatic NSCLC with disease progression following treatment with an EGFR TKI and are positive for the EGFR T790M mutation in China in January 2025. In April 2025, limertinib was also approved in China for first-line treatment for adult patients with locally advanced or metastatic NSCLC harbouring EGFR exon 19 deletions or exon 21 L858R mutations. This article summarizes the milestones in the development of limertinib leading to this first approval.
莱美替尼(奥益新)是一种口服的第三代表皮生长因子受体(EGFR)酪氨酸激酶抑制剂(TKI),已被开发用于治疗非小细胞肺癌(NSCLC)。在临床试验中,莱美替尼在T790M守门人突变呈阳性的患者中显示出疗效。2025年1月,莱美替尼在中国首次获批用于治疗经EGFR TKI治疗后疾病进展且EGFR T790M突变呈阳性的局部晚期或转移性NSCLC成人患者。2025年4月,莱美替尼在中国也被批准用于一线治疗携带EGFR外显子19缺失或外显子21 L858R突变的局部晚期或转移性NSCLC成人患者。本文总结了莱美替尼发展历程中促成这一首次获批的里程碑事件。