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KRASG12C抑制剂IBI351单药治疗晚期非小细胞肺癌患者的疗效和安全性:一项2期关键研究的结果

Efficacy and Safety of KRASG12C Inhibitor IBI351 Monotherapy in Patients With Advanced NSCLC: Results From a Phase 2 Pivotal Study.

作者信息

Zhou Qing, Meng Xiangjiao, Sun Longhua, Huang Dingzhi, Yang Nong, Yu Yan, Zhao Mingfang, Zhuang Wu, Guo Renhua, Hu Yi, Pan Yueyin, Shan Jinlu, Sun Meili, Yuan Ying, Fan Yun, Huang Jianan, Liu Lian, Chu Qian, Wang Xiuwen, Xu Chongrui, Lin Jiaxin, Huang Jingjing, Huang Mengna, Sun Jiya, Zhang Sujie, Zhou Hui, Wu Yi-Long

机构信息

Guangdong Lung Cancer Institute, Guangdong Provincial People's Hospital (Guangdong Academy of Medical Sciences), Southern Medical University, Guangzhou, People's Republic of China.

Radiotherapy Department, Shandong First Medical University Affiliated Cancer Hospital, Jinan, People's Republic of China.

出版信息

J Thorac Oncol. 2024 Dec;19(12):1630-1639. doi: 10.1016/j.jtho.2024.08.005. Epub 2024 Aug 9.

Abstract

INTRODUCTION

KRAS glycine-to-cysteine substitution at codon 12 (G12C) mutation is a well-recognized and increasingly promising therapeutic target with huge unmet clinical needs in NSCLC patients. IBI351 is a potent covalent and irreversible inhibitor of KRAS G12C. Here, we present the efficacy and safety of IBI351 from an open-label, single-arm, phase 2 pivotal study.

METHODS

Eligible patients with NSCLC with KRAS G12C who failed standard therapy were enrolled. IBI351 was orally administered at a dose of 600 mg twice daily. The primary endpoint was confirmed objective response rate assessed by an independent radiological review committee (IRRC) as per Response Evaluation Criteria in Solid Tumors v1.1. Other endpoints were safety, IRRC-confirmed disease control rate, duration of response, progression-free survival (PFS), and overall survival.

RESULTS

As of December 13, 2023, 116 patients were enrolled (Eastern Cooperative Oncology Group Performance Status 1: 91.4%; brain metastasis: 30.2%; prior treatments with both anti-PD-1 or anti-PD-L1 inhibitors and platinum-based chemotherapy: 84.5%). As per the IRRC assessment, the confirmed objective response rate was 49.1% (95% confidence interval [CI]: 39.7-58.6), and the disease control rate was 90.5% (95% CI: 83.7-95.2). The median duration of response was not reached whereas disease progression or death events occurred in 22 patients (38.6%), and the median PFS was 9.7 months (95% CI: 5.6-11.0). overall survival data was immature. Treatment-related adverse events (TRAEs) occurred in 107 patients (92.2%) whereas 48 patients (41.4%) had equal to or higher than grade three TRAEs. Common TRAEs were anemia (44.8%), increased alanine aminotransferase (28.4%), increased aspartate aminotransferase (27.6%), asthenia (26.7%) and presence of protein in urine (25.0%). TRAEs leading to treatment discontinuation occurred in nine patients (7.8%). In biomarker evaluable patients (n = 95), all patients had positive KRAS G12C in tissue whereas 72 patients were blood-positive and 23 were blood-negative for KRAS G12C. Patients with KRAS G12C in both blood and tissue had higher tumor burden at baseline (p < 0.05) and worse PFS (p < 0.05). Tumor mutation profiling identified tumor protein p53 (45.3%), serine/threonine kinase 11 (STK11) (30.5%), and kelch-like ECH-associated protein 1 (21.1%) as the most common genes co-mutated with KRAS G12C. Among 13 genes with mutation frequency equal to or higher than 5%, mutations of six genes (STK11, kelch-like ECH-associated protein 1, phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit gamma, DNA polymerase epsilon, SMAD family member 4, and BMP/retinoic acid-inducible neural-specific protein 3) were significantly associated with worse PFS (p < 0.05). Mutation in STK11 was also found to have a significant association with higher tumor burden at baseline and lower response rate (p < 0.05).

CONCLUSIONS

IBI351 monotherapy demonstrated promising and sustained efficacy with manageable safety, supporting its potential as a new treatment option for KRAS G12C-mutant NSCLC.

摘要

简介

KRAS基因第12密码子甘氨酸到半胱氨酸的替换(G12C)突变是一个公认的且越来越有前景的治疗靶点,在非小细胞肺癌(NSCLC)患者中存在巨大未满足的临床需求。IBI351是一种强效的、共价且不可逆的KRAS G12C抑制剂。在此,我们展示了来自一项开放标签、单臂、2期关键研究中IBI351的疗效和安全性。

方法

纳入符合条件的经标准治疗失败的KRAS G12C突变的NSCLC患者。IBI351以每日两次、每次600mg的剂量口服给药。主要终点是由独立放射学审查委员会(IRRC)根据实体瘤疗效评价标准第1.1版评估的确认客观缓解率。其他终点包括安全性、IRRC确认的疾病控制率、缓解持续时间、无进展生存期(PFS)和总生存期。

结果

截至2023年12月13日,共纳入116例患者(东部肿瘤协作组体能状态评分为1分的患者占91.4%;有脑转移的患者占30.2%;既往接受过抗PD - 1或抗PD - L1抑制剂以及铂类化疗的患者占84.5%)。根据IRRC评估,确认客观缓解率为49.1%(95%置信区间[CI]:39.7 - 58.6),疾病控制率为90.5%(95% CI:83.7 - 95.2)。缓解持续时间中位数未达到,而22例患者(38.6%)出现疾病进展或死亡事件,PFS中位数为9.7个月(95% CI:5.6 - 11.0)。总生存期数据尚不成熟。107例患者(92.2%)发生了治疗相关不良事件(TRAEs),其中48例患者(41.4%)发生了3级及以上TRAEs。常见的TRAEs包括贫血(44.8%)、丙氨酸氨基转移酶升高(28.4%)、天冬氨酸氨基转移酶升高(27.6%)、乏力(26.7%)和蛋白尿(25.0%)。导致治疗中断的TRAEs发生在9例患者(7.8%)中。在可进行生物标志物评估的患者(n = 95)中,所有患者组织中的KRAS G12C均为阳性,而72例患者血液中KRAS G12C为阳性,23例为阴性。血液和组织中均有KRAS G12C的患者基线时肿瘤负荷更高(p < 0.05),PFS更差(p < 0.05)。肿瘤突变谱分析确定肿瘤蛋白p53(45.3%)、丝氨酸/苏氨酸激酶11(STK11)(30.5%)和 Kelch样ECH相关蛋白1(21.1%)是与KRAS G12C共同突变最常见的基因。在突变频率等于或高于5%的13个基因中,6个基因(STK11、Kelch样ECH相关蛋白1、磷脂酰肌醇 - 4,5 - 二磷酸3 - 激酶催化亚基γ、DNA聚合酶ε、SMAD家族成员4和BMP/视黄酸诱导神经特异性蛋白3)的突变与更差的PFS显著相关(p < 0.05)。还发现STK11突变与基线时更高的肿瘤负荷和更低的缓解率显著相关(p < 0.05)。

结论

IBI351单药治疗显示出有前景且持续的疗效,安全性可控,支持其作为KRAS G12C突变型NSCLC新治疗选择的潜力。

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