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克唑替尼耐药 ROS1 重排非小细胞肺癌患者的色瑞替尼活性。

Activity of ceritinib in crizotinib-resistant ROS1-rearranged non-small-cell lung cancer patients.

机构信息

Department of Medical Oncology, The First Affiliated Hospital of Zhengzhou University, Zhengzhou City, Henan Province 450052, People's Republic of China.

出版信息

Medicine (Baltimore). 2023 Jul 21;102(29):e33543. doi: 10.1097/MD.0000000000033543.

Abstract

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.

摘要

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。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/af07/10662874/9f90d9361dc6/medi-102-e33543-g001.jpg

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