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Venous thromboembolic events with vascular endothelial growth factor receptor tyrosine kinase inhibitors: A systematic review and meta-analysis of randomized clinical trials

机译:血管内皮生长因子受体酪氨酸激酶抑制剂引起的静脉血栓栓塞事件:随机临床试验的系统评价和荟萃分析

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摘要

A trial-level meta-analysis was conducted to determine the relative risk (RR) of venous thromboembolic events (VTEs) associated with approved vascular endothelial growth factor receptor (VEGFR) tyrosine kinase inhibitors (TKI). Eligible studies included randomized phase 2 and 3 trials comparing arms with and without a Food and Drug Administration-approved VEGFR TKI (sunitinib, sorafenib, pazopanib, vandetanib, and axitinib). Statistical analyses calculated the RR and 95% confidence intervals (CI), using random-effects or fixed-effects models based on heterogeneity. A total of 7441 patients from 9 phase III trials and 8 phase II trials were selected. The RR of all grade and high-grade VTEs for the TKI vs. no TKI arms was 1.10 (95% CI 0.73-1.66, p=0.64) and 0.85 (95% CI: 0.58-1.25, p=0.41), respectively. No difference in risk was found based on tumor type, age and trial design. The majority of trials exhibited high quality per Jadad scoring and no heterogeneity or publication bias was found.
机译:进行了一项试验级荟萃分析,以确定与批准的血管内皮生长因子受体(VEGFR)酪氨酸激酶抑制剂(TKI)相关的静脉血栓栓塞事件(VTE)的相对风险(RR)。符合条件的研究包括2期和3期随机试验,比较有无食品和药物管理局批准的VEGFR TKI(舒尼替尼,索拉非尼,帕唑帕尼,vandetanib和axitinib)的组。统计分析使用基于异质性的随机效应或固定效应模型计算了RR和95%置信区间(CI)。从9项III期试验和8项II期试验中选择了7441例患者。 TKI与无TKI组相比,所有等级和高级VTE的RR分别为1.10(95%CI 0.73-1.66,p = 0.64)和0.85(95%CI:0.58-1.25,p = 0.41)。根据肿瘤类型,年龄和试验设计,未发现风险差异。大多数试验显示出Jadad评分的高质量,没有发现异质性或发表偏倚。

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