Sevabertinib in Advanced HER2 -Mutant Non–Small-Cell Lung Cancer

肺癌 不利影响 癌症 腹泻 医学 内科学 疾病 肿瘤科 肺 呼吸道疾病 临床试验
作者
Xiuning Le,Tae Min Kim,Herbert H. Loong,Arsela Prelaj,Boon Cher Goh,Lin Li,Yong Fang,Shun Lu,Xiaorong Dong,Lin Wu,Yuki Shinno,Gennaro Daniele,Tsung‐Ying Yang,Hye Ryun Kim,G. Ruiter,Jun Zhao,Silvia Novello,Liyun Miao,Pasi A. Jänne,Kōichi Goto
出处
期刊:The New England Journal of Medicine [Massachusetts Medical Society]
卷期号:393 (18): 1819-1832 被引量:61
标识
DOI:10.1056/nejmoa2511065
摘要

BACKGROUND: gene mutations occur in 2 to 4% of patients with non-small-cell lung cancer (NSCLC). Sevabertinib is an oral, reversible tyrosine kinase inhibitor that has shown anti-HER2 activity in preclinical models. METHODS: -mutant NSCLC. Three cohorts were defined according to previous therapy: cohort D comprised previously treated patients who had not received HER2-targeted therapy; cohort E, patients who had previously received HER2-directed antibody-drug conjugates; and cohort F, patients who had not previously received treatment. The primary end point was an objective response, as assessed by blinded independent central review. Secondary end points were duration of response and progression-free survival. RESULTS: A total of 209 patients received sevabertinib (as of June 27, 2025, the data-cutoff date); the median duration of follow-up was 13.8 months in cohort D, 11.7 months in cohort E, and 9.9 months in cohort F. Among 81 patients in cohort D, an objective response was observed in 64% (95% confidence interval [CI], 53 to 75); the median duration of response was 9.2 months (95% CI, 6.3 to 13.5), and the median progression-free survival was 8.3 months (95% CI, 6.9 to 12.3). Among 55 patients in cohort E, an objective response was observed in 38% (95% CI, 25 to 52); the median duration of response was 8.5 months, and the median progression-free survival was 5.5 months. Among 73 patients in cohort F, an objective response was observed in 71% (95% CI, 59 to 81), and the median duration of response was 11.0 months; data on progression-free survival were immature. Grade 3 or higher drug-related adverse events occurred in 31% of the patients. The most common adverse event was diarrhea (in 84 to 91%), with diarrhea of grade 3 or higher occurring in 5 to 23%. Treatment was discontinued by 3% of the patients owing to drug-related adverse events. CONCLUSIONS: -mutant NSCLC. Diarrhea was the most common adverse event. (Funded by Bayer; SOHO-01 ClinicalTrials.gov number, NCT05099172.).
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