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Efficacy of Aumolertinib (HS-10296) in Patients With Advanced EGFR T790M+ NSCLC: Updated Post-National Medical Products Administration Approval Results From the APOLLO Registrational Trial

医学 内科学 T790米 不利影响 临床终点 置信区间 胃肠病学 肿瘤科 临床试验 癌症 腺癌 ROS1型
作者
Shun Lü,Qiming Wang,Guojun Zhang,Xiaorong Dong,Cheng‐Ta Yang,Yong Song,Gee‐Chen Chang,You Lü,Hongming Pan,Chao‐Hua Chiu,Zhehai Wang,Jifeng Feng,Jianying Zhou,Xingxiang Xu,Renhua Guo,Jianhua Chen,Haihua Yang,Yuan Chen,Zhuang Yu,Her‐Shyong Shiah,Chin‐Chou Wang,Nong Yang,Jian Fang,Ping Wang,Kai Wang,Yanping Hu,Jianxing He,Ziping Wang,Jianhua Shi,Shaoshui Chen,Qiong Wu,Changan Sun,Chuan Li,Hongying Wei,Ying Cheng,Wu‐Chou Su,Te‐Chun Hsia,Jiuwei Cui,Yuping Sun,Sai‐Hong Ignatius Ou,Viola W. Zhu,James Chih‐Hsin Yang
出处
期刊:Journal of Thoracic Oncology [Elsevier]
卷期号:17 (3): 411-422 被引量:79
标识
DOI:10.1016/j.jtho.2021.10.024
摘要

Abstract

Introduction

Aumolertinib (formerly almonertinib; HS-10296) is a novel third-generation EGFR tyrosine kinase inhibitor (TKI) with revealed activity against EGFR-sensitizing mutations and EGFR T790M mutation.

Methods

Patients with locally advanced or metastatic NSCLC who developed an EGFR T790M mutation after progression on first- or second-generation EGFR TKI therapy were enrolled in this registrational phase 2 trial of aumolertinib at 110 mg orally once daily (NCT02981108). The primary end point was objective response rate (ORR) by independent central review.

Results

A total of 244 patients with EGFR T790M-positive NSCLC were enrolled. The ORR by independent central review was 68.9% (95% confidence interval [CI]: 62.6–74.6). The disease control rate was 93.4% (95% CI: 89.6–96.2). The median duration of response was 15.1 months (95% CI: 12.5–16.6). The median progression-free survival was 12.4 months (95% CI: 9.7–15.0). Among 23 patients with assessable central nervous system (CNS) metastases, the CNS-ORR and CNS-disease control rate were 60.9% (95% CI: 38.5–80.3) and 91.3% (95% CI: 72.0–98.9), respectively. The median CNS-duration of response was 12.5 months (95% CI: 5.6–not reached). Treatment-related adverse events of more than or equal to grade 3 occurred in 16.4% of the patients, with the most common being increased blood creatine phosphokinase level (7%) and increased alanine aminotransferase level (1.2%). The relative dose density of aumolertinib was 99.2% in this study.

Conclusions

Aumolertinib is an effective and well-tolerated third-generation EGFR TKI for patients with EGFR T790M-positive advanced NSCLC after disease progression on first- and second-generation EGFR TKI therapy. On the basis of these findings, aumolertinib was approved in the People's Republic of China for patients positive for EGFR T790M NSCLC.
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