Department of Medical Oncology, The First Affiliated Hospital of Zhengzhou University, Zhengzhou City, Henan Province 450052, People's Republic of China.
Medicine (Baltimore). 2023 Jul 21;102(29):e33543. doi: 10.1097/MD.0000000000033543.
As a second-generation selective oral anaplastic lymphoma kinase inhibitor, ceritinib is an effective first-line treatment for c-ros oncogene 1 (ROS1)-rearranged non-small-cell lung cancer (NSCLC). Its efficacy and safety for the treatment of crizotinib-resistant ROS1-rearranged NSCLC were explored in the study. A retrospective single-center study was conducted to investigate the efficacy of ceritinib in crizotinib-resistant ROS1-rearranged NSCLC. The objective response rate was the primary objective, while the disease control rate, progression-free survival and adverse events were secondary objectives. From December 2015 to October 2021, a total of 246 patients with ROS1-rearranged NSCLC were screened, 12 (4.9%) of whom were treated with ceritinib after the development of crizotinib resistance. Among the 12 crizotinib-resistant patients included, 3 displayed the efficacy of partial response and 3 had the efficacy of stable condition. The objective response rate, disease control rate and median progression-free survival of all patients were 25% (95% confidence interval [CI]: -3.7% to 53.7%; 3 of 12 patients), 50% (95% CI: 16.8% to 83.2%; 6 of 12 patients), and 10.5 months (95% CI, 5.7 to 15.3 months), respectively. In addition, of the 6 patients with brain metastases, an intracranial disease control rate of 66.7% (95% CI:12.5% to 120.9%) was obtained. The research results reveal that ceritinib can be a treatment option for ROS1-rearranged NSCLC patients after the development of crizotinib resistance.
作为第二代选择性口服间变性淋巴瘤激酶抑制剂,塞瑞替尼是一种有效的 c-ros 原癌基因 1(ROS1)重排非小细胞肺癌(NSCLC)的一线治疗药物。本研究旨在探讨塞瑞替尼治疗克唑替尼耐药 ROS1 重排 NSCLC 的疗效和安全性。一项回顾性单中心研究调查了塞瑞替尼在克唑替尼耐药 ROS1 重排 NSCLC 中的疗效。主要终点为客观缓解率,次要终点为疾病控制率、无进展生存期和不良事件。2015 年 12 月至 2021 年 10 月,共筛选出 246 例 ROS1 重排 NSCLC 患者,其中 12 例在克唑替尼耐药后接受了塞瑞替尼治疗。在这 12 例克唑替尼耐药患者中,3 例显示部分缓解疗效,3 例显示稳定病情疗效。所有患者的客观缓解率、疾病控制率和中位无进展生存期分别为 25%(95%置信区间[CI]:-3.7%至 53.7%;12 例患者中有 3 例)、50%(95%CI:16.8%至 83.2%;12 例患者中有 6 例)和 10.5 个月(95%CI,5.7 至 15.3 个月)。此外,6 例有脑转移的患者颅内疾病控制率为 66.7%(95%CI:12.5%至 120.9%)。研究结果表明,塞瑞替尼是克唑替尼耐药 ROS1 重排 NSCLC 患者的一种治疗选择。