Division of Hematology-Oncology, Samsung Medical Center, Sungkyunkwan University School of Medicine, Seoul, South Korea.
Division of Medical Oncology, Department of Internal Medicine, Yonsei Cancer Center, Yonsei University College of Medicine, Seoul, South Korea.
Clin Lung Cancer. 2022 Dec;23(8):720-730. doi: 10.1016/j.cllc.2022.07.008. Epub 2022 Jul 21.
Brigatinib is a next-generation anaplastic lymphoma kinase (ALK) inhibitor with demonstrated efficacy in locally advanced and metastatic non-small cell lung cancer (NSCLC) in crizotinib-refractory and ALK inhibitor-naive settings. This analysis assessed brigatinib in Asian vs. non-Asian patients from the first-line ALTA-1L trial.
This was a subgroup analysis from the phase III ALTA-1L trial of brigatinib vs. crizotinib in ALK inhibitor-naive ALK+ NSCLC. The primary endpoint was progression-free survival (PFS) as assessed by blinded independent review committee (BIRC). Secondary endpoints included confirmed objective response rate (ORR) and overall survival (OS) in the overall population and BIRC-assessed intracranial ORR and PFS in patients with brain metastases.
Of the 275 randomized patients, 108 were Asian. Brigatinib showed consistent superiority in BIRC-assessed PFS vs. crizotinib in Asian (hazard ratio [HR]: 0.35 [95% CI: 0.20-0.59]; log-rank P = .0001; median 24.0 vs. 11.1 months) and non-Asian (HR: 0.56 [95% CI: 0.38-0.84]; log-rank P = .0041; median 24.7 vs. 9.4 months) patients. Results were consistent with investigator-assessed PFS and BIRC-assessed intracranial PFS. Brigatinib was well tolerated. Toxicity profiles and dose modification rates were similar between Asian and non-Asian patients.
Efficacy with brigatinib was consistently better than with crizotinib in Asian and non-Asian patients with locally advanced or metastatic ALK inhibitor-naive ALK-+ NSCLC. There were no clinically notable differences in overall safety in Asian vs. non-Asian patients.
布加替尼是一种下一代间变性淋巴瘤激酶(ALK)抑制剂,在克唑替尼耐药和 ALK 抑制剂初治的局部晚期和转移性非小细胞肺癌(NSCLC)中显示出疗效。这项分析评估了一线 ALTA-1L 试验中亚洲与非亚洲患者使用布加替尼的情况。
这是一项来自 III 期 ALTA-1L 试验的亚组分析,比较了布加替尼与克唑替尼在 ALK 抑制剂初治的 ALK+ NSCLC 患者中的疗效。主要终点是由盲法独立审查委员会(BIRC)评估的无进展生存期(PFS)。次要终点包括总人群中确认的客观缓解率(ORR)和总生存期(OS),以及有脑转移患者的 BIRC 评估颅内 ORR 和 PFS。
在 275 名随机患者中,有 108 名是亚洲人。与克唑替尼相比,布加替尼在 BIRC 评估的 PFS 方面在亚洲人群(风险比 [HR]:0.35 [95%CI:0.20-0.59];对数秩 P=0.0001;中位 24.0 个月 vs. 11.1 个月)和非亚洲人群(HR:0.56 [95%CI:0.38-0.84];对数秩 P=0.0041;中位 24.7 个月 vs. 9.4 个月)中均显示出一致的优势。结果与研究者评估的 PFS 和 BIRC 评估的颅内 PFS 一致。布加替尼耐受性良好。亚洲和非亚洲患者的毒性谱和剂量调整率相似。
在局部晚期或转移性 ALK 抑制剂初治的 ALK+ NSCLC 亚洲和非亚洲患者中,布加替尼的疗效明显优于克唑替尼。亚洲和非亚洲患者的总体安全性无明显差异。