Central nervous system efficacy of aumolertinib versus gefitinib in patients with untreated, EGFR-mutated, advanced non-small cell lung cancer: data from a randomized phase III trial (AENEAS).

IF 20.1 1区 医学 Q1 ONCOLOGY
Shun Lu, Xiaorong Dong, Hong Jian, Jianhua Chen, Gongyan Chen, Yuping Sun, Yinghua Ji, Ziping Wang, Jianhua Shi, Junguo Lu, Shaoshui Chen, Dongqing Lv, Guojun Zhang, Chunling Liu, Juan Li, Xinmin Yu, Zhong Lin, Zhuang Yu, Zhehai Wang, Jiuwei Cui, Xingxiang Xu, Jian Fang, Jifeng Feng, Zhi Xu, Rui Ma, Jie Hu, Nong Yang, Xiangdong Zhou, Xiaohong Wu, Chengping Hu, Zhihong Zhang, You Lu, Yanping Hu, Liyan Jiang, Qiming Wang, Renhua Guo, Jianying Zhou, Baolan Li, Chunhong Hu, Wancheng Tong, Helong Zhang, Lin Ma, Yuan Chen, Zhijun Jie, Yu Yao, Longzhen Zhang, Jie Weng, Weidong Li, Jianping Xiong, Xianwei Ye, Jianchun Duan, Haihua Yang, Meili Sun, Hongying Wei, Jiawei Wei, Zheyu Zhang, Qiong Wu
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引用次数: 0

Abstract

Background: The initial randomized, double-blinded, actively controlled, phase III ANEAS study (NCT03849768) demonstrated that aumolertinib showed superior efficacy relative to gefitinib as first-line therapy in epidermal growth factor receptor (EGFR)-mutated advanced non-small cell lung cancer (NSCLC). Metastatic disease in the central nervous system (CNS) remains a challenge in the management of NSCLC. This study aimed to compare the efficacy of aumolertinib versus gefitinib among patients with baseline CNS metastases in the ANEAS study.

Methods: Eligible patients were enrolled and randomly assigned in a 1:1 ratio to orally receive either aumolertinib or gefitinib in a double-blinded fashion. Patients with asymptomatic, stable CNS metastases were included. Follow-up imaging of the same modality as the initial CNS imaging was performed every 6 weeks for 15 months, then every 12 weeks. CNS response was assessed by a neuroradiological blinded, independent central review (neuroradiological-BICR). The primary endpoint for this subgroup analysis was CNS progression-free survival (PFS).

Results: Of the 429 patients enrolled and randomized in the ANEAS study, 106 patients were found to have CNS metastases (CNS Full Analysis Set, cFAS) at baseline by neuroradiological-BICR, and 60 of them had CNS target lesions (CNS Evaluable for Response, cEFR). Treatment with aumolertinib significantly prolonged median CNS PFS compared with gefitinib in both cFAS (29.0 vs. 8.3 months; hazard ratio [HR] = 0.31; 95% confidence interval [CI], 0.17-0.56; P < 0.001) and cEFR (29.0 vs. 8.3 months; HR = 0.26; 95% CI, 0.11-0.57; P < 0.001). The confirmed CNS overall response rate in cEFR was 85.7% and 75.0% in patients treated with aumolertinib and gefitinib, respectively. Competing risk analysis showed that the estimated probability of CNS progression without prior non-CNS progression or death was consistently lower with aumolertinib than with gefitinib in patients with and without CNS metastases at baseline. No new safety findings were observed.

Conclusions: These results indicate a potential advantage of aumolertinib over gefitinib in terms of CNS PFS and the risk of CNS progression in patients with EGFR-mutated advanced NSCLC with baseline CNS metastases.

Trial registration: ClinicalTrials.gov number, NCT03849768.

未经治疗的表皮生长因子受体(EGFR)突变晚期非小细胞肺癌患者服用奥莫拉替尼和吉非替尼对中枢神经系统的疗效:一项随机III期试验(AENEAS)的数据。
研究背景最初的随机、双盲、积极对照的III期ANEAS研究(NCT03849768)表明,奥美乐替尼作为表皮生长因子受体(EGFR)突变的晚期非小细胞肺癌(NSCLC)的一线疗法,疗效优于吉非替尼。中枢神经系统(CNS)转移性疾病仍然是治疗NSCLC的一大挑战。本研究旨在比较ANEAS研究中基线中枢神经系统转移患者中奥莫拉替尼和吉非替尼的疗效:符合条件的患者被纳入研究,并以1:1的比例随机分配到口服奥美替尼或吉非替尼的双盲研究中。研究对象包括无症状、病情稳定的中枢神经系统转移患者。在15个月内,每6周进行一次与首次中枢神经系统成像相同的随访成像,之后每12周进行一次。中枢神经系统反应由神经放射学盲法独立中央审查(神经放射学-BICR)评估。该亚组分析的主要终点是中枢神经系统无进展生存期(PFS):在ANEAS研究中随机登记的429名患者中,有106名患者在基线时被神经放射学-BICR发现有中枢神经系统转移(中枢神经系统全分析集,cFAS),其中60名患者有中枢神经系统靶病变(中枢神经系统可评估反应,cEFR)。在cFAS(29.0个月对8.3个月;危险比[HR] = 0.31;95%置信区间[CI],0.17-0.56;P <0.001)和cEFR(29.0个月对8.3个月;HR = 0.26;95% CI,0.11-0.57;P <0.001)中,与吉非替尼相比,奥莫勒替尼治疗显著延长了中位CNS PFS。在cEFR中,接受奥美替尼和吉非替尼治疗的患者中枢神经系统总应答率分别为85.7%和75.0%。竞争风险分析表明,在基线有中枢神经系统转移灶和无中枢神经系统转移灶的患者中,使用奥莫拉替尼而无既往非中枢神经系统进展或死亡的中枢神经系统进展的估计概率一直低于吉非替尼。没有观察到新的安全性结果:这些结果表明,对于基线有中枢神经系统转移的表皮生长因子受体(EGFR)突变晚期NSCLC患者,奥莫拉替尼在中枢神经系统PFS和中枢神经系统进展风险方面比吉非替尼具有潜在优势:试验注册:ClinicalTrials.gov 编号:NCT03849768。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Cancer Communications
Cancer Communications Biochemistry, Genetics and Molecular Biology-Cancer Research
CiteScore
25.50
自引率
4.30%
发文量
153
审稿时长
4 weeks
期刊介绍: Cancer Communications is an open access, peer-reviewed online journal that encompasses basic, clinical, and translational cancer research. The journal welcomes submissions concerning clinical trials, epidemiology, molecular and cellular biology, and genetics.
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