Levine Cancer Institute, Atrium Health, Charlotte, NC 28210, USA.
Multidisciplinary Oncology & Therapeutic Innovations Department, Aix-Marseille University, CNRS, INSERM, CRCM, Marseille, 13007, France.
Future Oncol. 2021 May;17(14):1709-1719. doi: 10.2217/fon-2020-1119. Epub 2021 Feb 11.
Anaplastic lymphoma kinase (ALK) tyrosine kinase inhibitors (TKIs) have improved outcomes in -rearranged (ALK+) non-small-cell lung cancer (NSCLC). However, almost all patients eventually develop progressive disease on first-line ALK TKIs (e.g., crizotinib, alectinib and ceritinib). Brigatinib, a second-generation ALK TKI, may show efficacy in alectinib- and ceritinib-refractory ALK+ NSCLC. We describe the rationale and design of ALTA-2, a Phase II study of brigatinib in patients with locally advanced/metastatic ALK+ NSCLC and documented progressive disease on alectinib or ceritinib. The primary end point is confirmed objective response rate per independent review committee using response evaluation criteria in solid tumors version 1.1. Secondary end points include duration of response, progression-free survival, overall survival, safety and health-related quality of life.
间变性淋巴瘤激酶 (ALK) 酪氨酸激酶抑制剂 (TKI) 改善了融合基因阳性(ALK+)非小细胞肺癌 (NSCLC) 的预后。然而,几乎所有患者最终都会在一线 ALK TKI(如克唑替尼、阿来替尼和塞瑞替尼)治疗中出现疾病进展。第二代 ALK TKI 布加替尼可能对阿来替尼和塞瑞替尼耐药的 ALK+ NSCLC 有效。我们描述了 ALTA-2 的原理和设计,这是一项评估布加替尼治疗局部晚期/转移性 ALK+ NSCLC 患者的 II 期研究,这些患者在接受阿来替尼或塞瑞替尼治疗后疾病出现进展。主要终点是独立审查委员会根据实体瘤反应评价标准 1.1 评估的确认客观缓解率。次要终点包括缓解持续时间、无进展生存期、总生存期、安全性和健康相关生活质量。