安罗替尼治疗小细胞肺癌的临床应用与 研究进展
Clinical Application and Research Progress of Anlotinib in the Treatment of Small Cell Lung Cancer
DOI: 10.12677/acm.2026.1631090, PDF,   
作者: 张袁媛*:成都中医药大学医学与生命科学学院,四川 成都;陈耀华#:达州市中心医院呼吸与危重症医学科,四川 达州
关键词: 小细胞肺癌安罗替尼抗血管生成临床疗效联合治疗Small Cell Lung Cancer Anlotinib Anti-Angiogenesis Clinical Efficacy Combination Therapy
摘要: 小细胞肺癌(small cell lung cancer, SCLC)是一种高度侵袭性的肺癌类型,常伴随较差的预后,亟需有效的治疗方案。近年来,安罗替尼(Anlotinib)作为一种新型抗血管生成药物在小细胞肺癌患者的治疗中受到了广泛关注。其通过抑制血管内皮生长因子受体、成纤维细胞生长因子受体等多个靶点抑制肿瘤细胞的增殖、促进细胞凋亡以及抗肿瘤血管生成等机制,可能改善患者的生存率和生活质量。然而,其在临床应用中仍面临耐药性及个体差异等挑战。当前研究显示,安罗替尼在小细胞肺癌患者中具有一定的临床疗效,但其具体作用机制尚需进一步阐明。联合治疗策略有望提升安罗替尼疗效并优化治疗方案。本文系统综述安罗替尼在小细胞肺癌患者治疗中的应用,探讨其在小细胞肺癌中临床潜力,以期为临床实践提供参考。
Abstract: Small cell lung cancer (SCLC) is a highly aggressive type of lung cancer, often with a poor prognosis, and thus requires effective treatment options. In recent years, anlotinib, as a novel anti-angiogenic drug, has received considerable attention in the treatment of patients with small cell lung cancer. It inhibits tumor cell proliferation, promotes cell apoptosis, and blocks tumor angiogenesis through multiple targets such as vascular endothelial growth factor receptors and fibroblast growth factor receptors, potentially improving the survival rate and quality of life of patients. However, it still faces challenges such as drug resistance and individual differences in clinical application. Current studies show that anlotinib has certain clinical efficacy in patients with small cell lung cancer, but its specific mechanism of action still needs to be further clarified. Combined treatment strategies are expected to enhance the efficacy of anlotinib and optimize the treatment plan. This article systematically reviews the application of anlotinib in the treatment of small cell lung cancer patients, explores its clinical potential and future research directions, with the aim of providing a reference for clinical practice.
文章引用:张袁媛, 陈耀华. 安罗替尼治疗小细胞肺癌的临床应用与 研究进展[J]. 临床医学进展, 2026, 16(3): 2878-2888. https://doi.org/10.12677/acm.2026.1631090

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