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Apatinib as post second-line therapy in EGFR wild-type and ALK-negative advanced lung adenocarcinoma

机译:阿帕替尼作为​​EGFR野生型和ALK阴性晚期肺腺癌的二线治疗药物

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摘要

In the absence of a driver mutation, chemotherapy is the standard treatment option as first- and second-line therapy for advanced non-small-cell lung cancer (NSCLC). Though a large number of patients are suitable for post second-line therapies, the quality and quantity of the available drugs in this setting is poor. Apatinib, a small molecule vascular endothelial growth factor receptor-2 (VEGFR-2) tyrosine kinase inhibitor, is a first-generation oral antiangiogenesis drug approved in the People’s Republic of China for use as a subsequent line of treatment for advanced gastric cancer. Herein, we report three cases of advanced NSCLC with epidermal growth factor receptor wild-type and anaplastic lymphoma kinase-negative status, wherein the patients showed partial response to apatinib. Moreover, the three patients have achieved a progression-free survival of 2.8, 5.8, and 6 months, respectively. The main toxicities were hypertension, proteinuria, and hand–foot syndrome. Apatinib may provide an additional option for the treatment of advanced NSCLC, especially for advanced lung adenocarcinoma without a driver mutation.
机译:在没有驾驶员突变的情况下,化学疗法是晚期非小细胞肺癌(NSCLC)的一线和二线治疗的标准治疗选择。尽管大量患者适合进行二线治疗,但在这种情况下可用药物的质量和数量都很差。阿帕替尼是一种小分子血管内皮生长因子受体2(VEGFR-2)酪氨酸激酶抑制剂,是经中华人民共和国批准的第一代口服抗血管生成药物,可用于晚期胃癌的后续治疗。本文中,我们报告了3例具有表皮生长因子受体野生型和间变性淋巴瘤激酶阴性状态的晚期NSCLC患者,其中患者对阿帕替尼表现出部分反应。此外,三名患者分别获得了2.8、5.8和6个月的无进展生存期。主要毒性为高血压,蛋白尿和手足综合症。阿帕替尼可能为晚期NSCLC的治疗提供额外的选择,特别是对于无驱动突变的晚期肺腺癌。

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