Zha Bowen, Zhang Yuxin, Yang Runzi, Kamili Muladili
Department of Education, Beijing Anzhen Hospital, Capital Medical University, Beijing 100029, P.R. China.
Department of Evidence-Based Medicine, School of Public Health, Capital Medical University, Beijing 100069, P.R. China.
Oncol Lett. 2022 May 27;24(1):229. doi: 10.3892/ol.2022.13350. eCollection 2022 Jul.
Anlotinib is a novel multitarget tyrosine kinase inhibitor, which has been indicated to inhibit both tumor angiogenesis and signal transduction pathways associated with proliferation. The main proposed mechanism of anlotinib inhibiting tumor angiogenesis is that anlotinib inhibits the activation of VEGFR2, PDGFRβ and FGFR1, and downstream ERK signal transduction. The aim of the present study was to systematically evaluate the efficacy and safety of third-line treatment with anlotinib for advanced non-small cell lung cancer (NSCLC). To meet this aim, studies published up to February 2022 were searched in PubMed, Web of Science, the Cochrane Library and several Chinese databases. Only randomized controlled trials (RCTs) were included and a metaanalysis was performed using RevMan 5.3 software. A total of 18 RCTs were identified and included in the present study, comprising 1,658 patients. The anlotinib treatment group was indicated to be better than the control group at prolonging progression-free survival [hazard ratio (HR), 0.33; 95% confidence interval (95% CI), 0.28-0.37] and overall survival (HR, 0.70; 95% CI, 0.60-0.81). Anlotinib also provided a significant improvement in the disease control rate [risk ratio (RR), 1.51; 95% CI, 1.27-1.79], objective response rate (1.75, 95% CI, 1.51-2.03) and Karnofsky performance status (mean difference, 9.85; 95% CI, 6.26-13.43). Compared with the control group, the incidence of adverse events (AEs), such as hypertension and hemoptysis, was increased by anlotinib. Through subgroup analysis, it was determined that, compared with the placebo, the incidence of AEs was increased by anlotinib, although compared with other therapeutic drugs, no significant differences were observed. In conclusion, the findings of the present study suggested that the thirdline treatment of advanced NSCLC with anlotinib is more effective compared with other control measures and that the AEs are also controllable. However, given the limitations of the quantity and the quality of the included studies, further studies are required to gain a more complete understanding of the effects of anlotinib.
安罗替尼是一种新型多靶点酪氨酸激酶抑制剂,已被证实可抑制肿瘤血管生成以及与增殖相关的信号转导通路。安罗替尼抑制肿瘤血管生成的主要机制是其抑制血管内皮生长因子受体2(VEGFR2)、血小板衍生生长因子受体β(PDGFRβ)和成纤维细胞生长因子受体1(FGFR1)的激活以及下游的细胞外信号调节激酶(ERK)信号转导。本研究的目的是系统评价安罗替尼用于晚期非小细胞肺癌(NSCLC)三线治疗的疗效和安全性。为实现这一目的,检索了截至2022年2月在PubMed、科学网、考克兰图书馆以及几个中文数据库中发表的研究。仅纳入随机对照试验(RCT),并使用RevMan 5.3软件进行荟萃分析。共确定18项RCT并纳入本研究,包括1658例患者。结果表明,安罗替尼治疗组在延长无进展生存期[风险比(HR),0.33;95%置信区间(95%CI),0.28 - 0.37]和总生存期(HR,0.70;95%CI,0.60 - 0.81)方面优于对照组。安罗替尼在疾病控制率[风险比(RR),1.51;95%CI,1.27 - 1.79]、客观缓解率(1.75,95%CI,1.51 - 2.03)和卡氏功能状态评分(平均差值,9.85;95%CI,6.26 - 13.43)方面也有显著改善。与对照组相比,安罗替尼增加了高血压和咯血等不良事件(AE)的发生率。通过亚组分析确定,与安慰剂相比,安罗替尼增加了AE的发生率,不过与其他治疗药物相比,未观察到显著差异。总之,本研究结果表明,安罗替尼用于晚期NSCLC的三线治疗比其他对照措施更有效,且AE也是可控的。然而,鉴于纳入研究的数量和质量存在局限性,需要进一步研究以更全面地了解安罗替尼的作用。