铈替尼
阿列克替尼
克里唑蒂尼
间变性淋巴瘤激酶
医学
肺癌
内科学
肿瘤科
碱性抑制剂
恶性胸腔积液
作者
Edward S. Kim,Fabrice Barlési,Tony Mok,Myung‐Ju Ahn,Jiayu Shen,Pingkuan Zhang,Sai‐Hong Ignatius Ou
出处
期刊:Future Oncology
[Future Medicine]
日期:2021-02-11
卷期号:17 (14): 1709-1719
被引量:11
标识
DOI:10.2217/fon-2020-1119
摘要
Anaplastic lymphoma kinase (ALK) tyrosine kinase inhibitors (TKIs) have improved outcomes in ALK-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.
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