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首页> 外文期刊>Journal of Clinical Oncology >Risk of arterial thromboembolic events with sunitinib and sorafenib: a systematic review and meta-analysis of clinical trials.
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Risk of arterial thromboembolic events with sunitinib and sorafenib: a systematic review and meta-analysis of clinical trials.

机译:舒尼替尼和索拉非尼发生动脉血栓栓塞事件的风险:临床试验的系统评价和荟萃分析。

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PURPOSE: Sunitinib and sorafenib are oral vascular endothelial growth factor receptor (VEGFR) tyrosine kinase inhibitors (TKIs) used in a vast range of cancers. Arterial thromboembolic events (ATE) have been described with these agents, although the overall risk remains unclear. We did a systematic review and meta-analysis to determine the incidence and the relative risk (RR) associated with the use of sunitinib and sorafenib. PATIENTS AND METHODS: PubMed databases were searched for articles published from January 1966 to July 2009, and abstracts presented at the American Society of Clinical Oncology (ASCO) and the European Society of Medical Oncology (ESMO) meetings held between 2004 and 2009 were searched for relevant clinical trials. Eligible studies included phase II and III trials and expanded access programs. Statistical analyses were conducted to calculate the summary incidence, RRs, and 95% CIs, using random-effects or fixed-effects models based on the heterogeneity of included studies. RESULTS: A total of 10,255 patients were selected for this meta-analysis. The incidence for ATE was 1.4% (95% CI, 1.2% to 1.6%). The RR of ATEs associated with sorafenib and sunitinib was 3.03 (95% CI, 1.25 to 7.37; P = .015) compared with control patients. The analysis was also stratified for the underlying malignancy (renal cell cancer v non-renal cell cancer) and TKI (sunitinib v sorafenib), but no significant differences in incidence or RR were observed. CONCLUSION: Treatment with VEGFR TKIs sunitinib and sorafenib is associated with a significant increase in the risk of ATEs.
机译:目的:舒尼替尼和索拉非尼是广泛用于多种癌症的口服血管内皮生长因子受体(VEGFR)酪氨酸激酶抑制剂(TKI)。尽管总体风险尚不清楚,但已经描述了使用这些药物的动脉血栓栓塞事件(ATE)。我们进行了系统的回顾和荟萃分析,以确定与舒尼替尼和索拉非尼的使用相关的发生率和相对危险度(RR)。病人和方法:检索PubMed数据库以查找1966年1月至2009年7月发表的文章,并检索在2004年至2009年举行的美国临床肿瘤学会(ASCO)和欧洲医学肿瘤学会(ESMO)会议上发表的摘要。相关的临床试验。符合条件的研究包括II期和III期试验以及扩展的访问计划。根据纳入研究的异质性,使用随机效应或固定效应模型进行统计分析,以计算汇总发生率,RR和95%CI。结果:总共选择了10255例患者进行荟萃分析。 ATE的发生率为1.4%(95%CI,1.2%至1.6%)。与对照组相比,与索拉非尼和舒尼替尼相关的ATEs的RR为3.03(95%CI,1.25至7.37; P = .015)。对潜在的恶性肿瘤(肾细胞癌对非肾细胞癌)和TKI(舒尼替尼对索拉非尼)进行了分层分析,但未观察到发病率或RR的显着差异。结论:VEGFR TKIs舒尼替尼和索拉非尼治疗与ATE风险显着增加有关。

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