Department of Respiratory and Critical Care Medicine, Peking Union Medical College Hospital, Chinese Academy of Medical Sciences and Peking Union Medical College, No. 1 Shuaifuyuan, Dongcheng District, Beijing, China.
National Taiwan University Hospital and National Taiwan University Cancer Center, Taipei, Taiwan.
Cancer Discov. 2022 Jul 6;12(7):1676-1689. doi: 10.1158/2159-8290.CD-21-1615.
Epidermal growth factor receptor exon 20 insertion mutations (EGFRexon20ins) are detected in approximately 2% of patients with non-small cell lung cancer (NSCLC). Due to a lack of effective therapy, the prognosis of these patients is typically poor. Sunvozertinib (DZD9008) was designed as an oral, potent, irreversible, and selective EGFR tyrosine kinase inhibitor, showing activity against EGFRexon20ins and other mutations. In both cell lines and xenograft models, sunvozertinib shows potent antitumor activity. In the two ongoing phase I clinical studies, sunvozertinib was tolerated up to 400 mg once daily. The most common drug-related adverse events included diarrhea and skin rash. Antitumor efficacy was observed at the doses of 100 mg and above in patients with EGFRexon20ins NSCLC across different subtypes, with prior amivantamab treatment as well as with baseline brain metastasis. The median duration of response has not been reached.
We report the discovery and early clinical development of sunvozertinib, a potential treatment option for the unmet medical need of EGFRexon20ins NSCLC. This article is highlighted in the In This Issue feature, p. 1599.
表皮生长因子受体外显子 20 插入突变(EGFRexon20ins)约占非小细胞肺癌(NSCLC)患者的 2%。由于缺乏有效的治疗方法,这些患者的预后通常较差。Sunvozertinib(DZD9008)被设计为一种口服、强效、不可逆和选择性的表皮生长因子受体酪氨酸激酶抑制剂,对 EGFRexon20ins 和其他突变具有活性。在细胞系和异种移植模型中,sunvozertinib 均显示出强大的抗肿瘤活性。在两项正在进行的 I 期临床研究中,sunvozertinib 每天一次口服至 400mg 时可耐受。最常见的药物相关不良事件包括腹泻和皮疹。在不同亚型的 EGFRexon20ins NSCLC 患者中,剂量为 100mg 及以上时观察到抗肿瘤疗效,包括先前接受 amivantamab 治疗以及存在基线脑转移的患者。反应的中位持续时间尚未达到。
我们报告了 sunvozertinib 的发现和早期临床开发,这是一种针对 EGFRexon20ins NSCLC 未满足医疗需求的潜在治疗选择。本文在本期特色文章中重点介绍,第 1599 页。