National University Hospital, Singapore.
National Cancer Centre, Singapore.
Lung Cancer. 2022 Jul;169:67-76. doi: 10.1016/j.lungcan.2022.05.012. Epub 2022 May 23.
To analyze the efficacy and safety of lorlatinib in Asian and non-Asian patients with pretreated anaplastic lymphoma kinase (ALK)-positive, advanced non-small cell lung cancer (NSCLC) from a phase 1/2 study.
In this ongoing phase 2 part of the trial, patients with ALK- or ROS1-positive, advanced NSCLC enrolled into six expansion cohorts (EXP1-6), based on ALK and ROS1 status and previous therapy, and received lorlatinib 100 mg once daily. The primary endpoint was objective tumor response and intracranial response. Post hoc analyses of activity were conducted in Asian and non-Asian (based on race) ALK-positive patients who received either previous crizotinib with or without chemotherapy (EXP2-3A) or at least one second-generation ALK tyrosine kinase inhibitor with any number of chemotherapy regimens (EXP3B-5). Analysis of safety (adverse events [AEs]) was in the phase 1 and 2 study population who started lorlatinib 100 mg once daily.
17 Asian patients were enrolled in EXP2-3A and 53 in EXP3B-5; 33 non-Asian patients were enrolled in EXP2-3A and 73 in EXP3B-5. Objective response rates in the Asian and non-Asian subgroups were 82.4% (95% confidence interval [CI]: 56.6-96.2) and 63.6% (95% CI: 45.1-79.6) in EXP2-3A, and 47.2% (95% CI: 33.3-61.4) and 30.1% (95% CI: 19.9-42.0) in EXP3B-5, and median progression-free survival was 13.6 and 12.5 months (EXP2-3A) and 6.9 and 5.5 months (EXP3B-5). Lorlatinib exhibited antitumor activity across ALK resistance mutations, while no differences according to the EML4-ALK variant could be detected. The most common treatment-related AEs were hypercholesterolemia, hypertriglyceridemia, edema, and peripheral neuropathy in both Asian and non-Asian subgroups.
Lorlatinib showed substantial overall and intracranial activity in pretreated patients with ALK-positive NSCLC in both Asian and non-Asian patients. AE profiles were similar between Asian and non-Asian patients.
gov NCT01970865.
分析预处理间变性淋巴瘤激酶(ALK)阳性、晚期非小细胞肺癌(NSCLC)亚洲和非亚洲患者中洛拉替尼的疗效和安全性,该研究来自一项 1/2 期研究。
在这项试验的 2 期部分的持续进行中,根据 ALK 和 ROS1 状态和既往治疗情况,入组了 6 个扩展队列(EXP1-6)的 ALK 或 ROS1 阳性、晚期 NSCLC 患者,并接受洛拉替尼 100mg 每日一次治疗。主要终点是客观肿瘤缓解和颅内缓解。对既往接受过克唑替尼联合或不联合化疗(EXP2-3A)或至少一种第二代 ALK 酪氨酸激酶抑制剂联合任意数量化疗方案(EXP3B-5)的 ALK 阳性患者进行了疗效的事后分析。安全性(不良事件 [AE])分析纳入了开始接受洛拉替尼 100mg 每日一次治疗的 1 期和 2 期研究人群。
EXP2-3A 中纳入了 17 名亚洲患者和 53 名非亚洲患者,EXP3B-5 中分别纳入了 53 名和 73 名。EXP2-3A 中,亚洲和非亚洲亚组的客观缓解率分别为 82.4%(95%置信区间 [CI]:56.6-96.2)和 63.6%(95% CI:45.1-79.6),EXP3B-5 中分别为 47.2%(95% CI:33.3-61.4)和 30.1%(95% CI:19.9-42.0),中位无进展生存期分别为 13.6 和 12.5 个月(EXP2-3A)和 6.9 和 5.5 个月(EXP3B-5)。洛拉替尼在ALK 耐药突变中表现出抗肿瘤活性,而 EML4-ALK 变异体之间无差异。最常见的治疗相关不良反应为亚洲和非亚洲亚组的高胆固醇血症、高甘油三酯血症、水肿和周围神经病。
洛拉替尼在亚洲和非亚洲 ALK 阳性 NSCLC 预处理患者中表现出显著的总体和颅内活性。AE 谱在亚洲和非亚洲患者之间相似。
gov NCT01970865。