Lorlatinib for Previously Treated ALK-Positive Advanced NSCLC: Primary Efficacy and Safety From a Phase 2 Study in People’s Republic of China

医学 队列 克里唑蒂尼 内科学 临床终点 肺癌 置信区间 肿瘤科 胃肠病学 外科 临床试验 恶性胸腔积液
作者
Shun Lü,Qing Zhou,Xiaoqing Liu,Yingying Du,Yun Fan,Ying Cheng,Jian Fang,You Lü,Cheng Zhi Huang,Jianying Zhou,Yong Song,Kai Wang,Hongming Pan,Nong Yang,Juan Li,Gongyan Chen,Jianhua Chang,Jiuwei Cui,Zhe Liu,Chunxue Bai
出处
期刊:Journal of Thoracic Oncology [Elsevier]
卷期号:17 (6): 816-826 被引量:26
标识
DOI:10.1016/j.jtho.2022.02.014
摘要

IntroductionLorlatinib was found to have activity in ALK-positive NSCLC in a global phase 1 and 2 study. We report an ongoing phase 2 study in Chinese patients with ALK-positive advanced or metastatic NSCLC.MethodsOpen-label, dual-cohort study (NCT03909971); patients had progressive disease after ALK tyrosine kinase inhibitor treatment (cohort 1: previous crizotinib; cohort 2: one ALK tyrosine kinase inhibitor other than crizotinib [±prior crizotinib]), more than or equal to one unirradiated extracranial target lesion, and Eastern Cooperative Oncology Group performance status of 0 to 2. Patients received oral lorlatinib 100 mg once daily in continuous 21-day cycles. Primary end point: objective response in cohort 1 by independent central radiology (ICR) according to Response Evaluation Criteria in Solid Tumors version 1.1. Analyses were based on patients receiving more than or equal to one dose.ResultsAt data cutoff (August 10, 2020), 109 patients were enrolled (cohort 1: n = 67; cohort 2: n = 42). A total of 47 patients in cohort 1 (70.1%, 95% confidence interval [CI]: 57.7–80.7, p < 0.0001; primary end point) and 20 patients in cohort 2 (47.6%, 95% CI: 32.0–63.6, secondary end point) achieved objective response by ICR. Median progression-free survival was not reached in cohort 1 and was 5.6 months in cohort 2. In patients with brain lesions at baseline, 29 of 36 patients in cohort 1 (80.6%, 95% CI: 64.0–91.8) and 10 of 21 patients in cohort 2 (47.6%, 95% CI: 25.7–70.2) achieved objective intracranial response by ICR. Hypercholesterolemia (92.7%) and hypertriglyceridemia (90.8%) (cluster terms) were common treatment-related adverse events (TRAEs). Nine patients (8.3%) had serious TRAEs; one permanently discontinued from treatment because of TRAEs.ConclusionsLorlatinib was found to have a robust and durable response and high intracranial objective response in previously treated Chinese patients with ALK-positive NSCLC.

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