Kato Yu
Tsukuba Research Laboratories, Eisai Co., Ltd., Tsukuba, Ibaraki, Japan.
Int J Clin Oncol. 2025 Apr;30(4):666-673. doi: 10.1007/s10147-025-02721-5. Epub 2025 Feb 22.
Lenvatinib is an orally available multi-tyrosine kinase inhibitor that mainly targets vascular endothelial growth factor (VEGF) and fibroblast growth factor (FGF) signaling. These inhibitory activities of lenvatinib exhibit antitumor efficacy, mainly due to their repressive effects on angiogenesis. In addition, a recent non-clinical evaluation using mouse tumor models revealed that lenvatinib causes immunomodulatory effects, including activation of effector T-cells and regulation of tumor-associated macrophages (TAMs). Combined treatment with lenvatinib and anti-programmed cell death-1 antibody (anti-PD-1) resulted in enhanced antitumor activity relative to monotreatment with anti-PD-1 or lenvatinib. This review summarizes the antitumor mechanisms of lenvatinib and of lenvatinib plus anti-PD-1 combination therapy.
乐伐替尼是一种口服多靶点酪氨酸激酶抑制剂,主要作用于血管内皮生长因子(VEGF)和成纤维细胞生长因子(FGF)信号通路。乐伐替尼的这些抑制活性具有抗肿瘤疗效,主要是因为它们对血管生成具有抑制作用。此外,最近一项使用小鼠肿瘤模型的非临床评估显示,乐伐替尼具有免疫调节作用,包括激活效应T细胞和调节肿瘤相关巨噬细胞(TAM)。与抗程序性细胞死亡蛋白1抗体(抗PD-1)联合治疗相对于单独使用抗PD-1或乐伐替尼具有更强的抗肿瘤活性。本综述总结了乐伐替尼以及乐伐替尼联合抗PD-1治疗的抗肿瘤机制。