Efficacy and Safety of Rezivertinib (BPI-7711) in Patients With Locally Advanced or Metastatic/Recurrent EGFR T790M-Mutated NSCLC: A Phase 2b Study

医学 T790米 内科学 临床终点 肿瘤科 无进展生存期 置信区间 临床研究阶段 中止 进行性疾病 临床试验 化疗 表皮生长因子受体 癌症 吉非替尼
作者
Yuankai Shi,Shiman Wu,Ke Wang,Shundong Cang,Wenxiu Yao,Yun Fan,Lin Wu,Meijuan Huang,Xingya Li,Yueyin Pan,Zhixiong Yang,Bo Zhu,Gongyan Chen,Jianhua Shi,Meili Sun,Jian Fang,Lijun Wang,Zhaohong Chen,Chunling Liu,Jingzhang Li,Jiwei Liu,Shenghua Sun,Yanqiu Zhao,Yanzhen Guo,Zili Meng,Zhefeng Liu,Zhigang Han,Hong Lü,Rui Ma,Sheng Hu,Guofang Zhao,Zheng Liu,Congying Xie,Diansheng Zhong,Hui Zhao,Huiqing Yu,Longzhen Zhang,Minghong Bi,Shanyong Yi,Shuliang Guo,Tienan Yi,Wen Li,Yingcheng Lin,Yongqian Shu,Zhendong Chen,Zhongliang Guo,Michael N. Greco,Tingting Wang,Haijiao Shen
出处
期刊:Journal of Thoracic Oncology [Elsevier]
卷期号:17 (11): 1306-1317 被引量:15
标识
DOI:10.1016/j.jtho.2022.08.015
摘要

IntroductionRezivertinib (BPI-7711) is a novel third-generation EGFR tyrosine kinase inhibitor (TKI) targeting both EGFR-sensitizing mutations and EGFR T790M mutation. This study aimed to evaluate the efficacy and safety of rezivertinib in patients with locally advanced or metastatic/recurrent EGFR T790M-mutated NSCLC.MethodsPatients with locally advanced or metastatic/recurrent NSCLC with confirmed EGFR T790M mutation who progressed after first-/second-generation EGFR TKI therapy or primary EGFR T790M mutation were enrolled. Patients received rezivertinib at 180 mg orally once daily until disease progression, unacceptable toxicity, or withdrawal of consent. The primary end point was objective response rate (ORR) assessed by blinded independent central review per Response Evaluation Criteria in Solid Tumors version 1.1. Secondary end points included disease control rate (DCR), duration of response, progression-free survival (PFS), overall survival, and safety. This study is registered with Clinical Trials.gov (NCT03812809).ResultsA total of 226 patients were enrolled from July 5, 2019, to January 22, 2020. By the data cutoff date on January 24, 2022, the median duration of follow-up was 23.3 months (95% confidence interval [CI]: 22.8–24.0). The ORR by blinded independent central review was 64.6% (95% CI: 58.0%–70.8%), and DCR was 89.8% (95% CI: 85.1%–93.4%). The median duration of response was 12.5 months (95% CI: 10.0–13.9), and median PFS was 12.2 months (95% CI: 9.6–13.9). The median overall survival was 23.9 months (95% CI: 20.0–not calculated [NC]). Among 91 (40.3%) patients with central nervous system (CNS) metastases, the median CNS PFS was 16.6 months (95% CI: 11.1–NC). In 29 patients with more than or equal to one brain target lesion at baseline, the CNS ORR and CNS DCR were 69.0% (95% CI: 49.2%–84.7%) and 100% (95% CI: 88.1%–100%), respectively. Time to progression of CNS was 16.5 months (95% CI: 9.7–NC). Of 226 patients, 188 (83.2%) had at least one treatment-related adverse event, whereas grade more than or equal to 3 occurred in 45 (19.9%) patients. No interstitial lung disease was reported.ConclusionsRezivertinib was found to have promising efficacy and favorable safety profile for patients with locally advanced or metastatic/recurrent NSCLC with EGFR T790M mutation.
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