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Apatinib monotherapy for advanced non‐small cell lung cancer after the failure of chemotherapy or other targeted therapy

机译:化疗或其他靶向治疗失败后的阿帕替尼单药治疗晚期非小细胞肺癌

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Background Apatinib, a small‐molecule inhibitor of vascular endothelial growth factor receptor 2 (VEGFR‐2), has proven to be effective and safe for treating patients with advanced gastric cancer after second‐line chemotherapy failure. As VEGFR‐2 targeted therapy has made encouraging progress for the treatment of a broad range of malignancies, we explored the efficacy and safety of apatinib for the treatment of advanced non‐small cell lung cancer after the failure of chemotherapy or other targeted therapy. Methods We retrospectively analyzed the data of 34 patients (11 with squamous carcinoma and 23 with adenocarcinoma) who were treated with apatinib alone in a daily oral dose of 250 mg in the second‐line or third‐line setting from January 2016 to July 2017. The primary endpoint was progression‐free survival (PFS). Results EGFR mutation or amplification was detected in 15 patients. The median PFS of the whole group was four months (95% confidence interval 0.3–7.7). A partial response was observed in 2 patients (5.88%) and stable disease in 19 (55.88%). The disease control rate was 61.76%. Common side effects of apatinib were hypertension ( n = 12), hand‐foot syndrome ( n = 8), and proteinuria ( n = 5), which accounted for 35.30%, 23.53%, and 14.71%, respectively, and no grade 3/4 adverse reactions occurred. Apatinib toxicity was controllable and tolerable. Conclusions Apatinib appears to be effective and safe for advanced non‐small cell lung cancer after the failure of chemotherapy or other targeted therapy.
机译:背景技术阿帕替尼是血管内皮生长因子受体2(VEGFR-2)的小分子抑制剂,已被证明对二线化疗失败后的晚期胃癌患者有效且安全。由于VEGFR-2靶向疗法在治疗各种恶性肿瘤方面取得了令人鼓舞的进展,因此我们探索了在化疗或其他靶向疗法失败后阿帕替尼治疗晚期非小细胞肺癌的疗效和安全性。方法我们回顾性分析了2016年1月至2017年7月在二线或三线治疗中每日口服250 mg阿帕替尼单独治疗的34例患者(11例鳞状癌和23例腺癌)的数据。主要终点是无进展生存期(PFS)。结果15例患者中检测到EGFR突变或扩增。整个组的中位PFS为四个月(95%置信区间0.3-7.7)。 2例患者(5.88%)观察到部分反应,19例患者病情稳定(55.88%)。疾病控制率为61.76%。阿帕替尼的常见副作用为高血压(n = 12),手足综合征(n = 8)和蛋白尿(n = 5),分别占35.30%,23.53%和14.71%,且没有3级/ 4发生不良反应。阿帕替尼的毒性是可控和可耐受的。结论在化疗或其他靶向治疗失败后,阿帕替尼对晚期非小细胞肺癌似乎是有效和安全的。

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