| Literature DB >> 35404393 |
Mengzhao Wang1, James Chih-Hsin Yang2, Paul L Mitchell3, Jian Fang4, D Ross Camidge5, Weiqi Nian6, Chao-Hua Chiu7, Jianying Zhou8, Yanqiu Zhao9, Wu-Chou Su10, Tsung-Ying Yang11, Viola W Zhu12, Michael Millward13, Yun Fan14, Wen-Tsung Huang15, Ying Cheng16, Liyan Jiang17, Daniel Brungs18, Lyudmila Bazhenova19, Chee Khoon Lee20, Bo Gao21, Yan Xu1, Wei-Hsun Hsu22, Li Zheng23, Pasi A Jänne24.
Abstract
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. SIGNIFICANCE: 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. ©2022 The Authors; Published by the American Association for Cancer Research.Entities:
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Year: 2022 PMID: 35404393 PMCID: PMC9262839 DOI: 10.1158/2159-8290.CD-21-1615
Source DB: PubMed Journal: Cancer Discov ISSN: 2159-8274 Impact factor: 38.272