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首页> 外文期刊>Canadian journal of gastroenterology & hepatology. >The Cost-Effectiveness of Lenvatinib in the Treatment of Advanced or Unresectable Hepatocellular Carcinoma from a Canadian Perspective
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The Cost-Effectiveness of Lenvatinib in the Treatment of Advanced or Unresectable Hepatocellular Carcinoma from a Canadian Perspective

机译:Lenvatinib在加拿大视角治疗先进或不可切除的肝细胞癌中的成本效益

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Lenvatinib is an oral multikinase inhibitor indicated for the first-line treatment of unresectable hepatocellular carcinoma (uHCC). In the Phase III REFLECT trial, lenvatinib was noninferior in the primary endpoint of overall survival versus sorafenib, the only systemic therapy funded in Canada prior to the introduction of lenvatinib. Lenvatinib also demonstrated statistically significant improvement compared to sorafenib in secondary endpoint progression-free survival, time to progression, and objective response rate. The aim of this analysis was to estimate the cost-effectiveness of lenvatinib versus sorafenib for the first-line treatment of patients with uHCC from a Canadian perspective. A cost-utility analysis was conducted using partitioned survival modelling, with health states representing progression-free disease, progressed disease, and death. Health effects were measured using quality-adjusted life years (QALYs), and costs were represented in Canadian dollars. Clinical inputs were derived from the REFLECT trial, with outcomes extrapolated using parametric survival models. EQ-5D data collected in REFLECT were used to determine health state utility values, and estimates of resource use came from a survey of clinicians. The model predicted incremental costs of-$5,021 and incremental QALYs of 0.17, making lenvatinib dominant over sorafenib. The model demonstrates lenvatinib to be a cost-effective use of resources versus sorafenib in Canada for the treatment of uHCC. Overall costs are lower compared with sorafenib, while health benefits are greater, with modelled progression-free and overall survival extended by 4.1 and 2.6 months in the lenvatinib arm, respectively.
机译:Lenvatinib是一种口服多立蛋白酶抑制剂,表明不可切除的肝细胞癌(UHCC)的一线处理。在III期反映试验中,Lenvatinib在整体存活的主要终点中是非索拉非尼的终点,在引入Lenvatinib之前在加拿大提供的唯一全身治疗。 Lenvatinib还在次要终点进入的无进展生存期,进展时间和客观反应率时显示出统计学上显着的改善。该分析的目的是估算Lenvatinib对索拉非尼的成本效益,用于从加拿大角度来看UHCC患者的一线治疗。使用分区存活建模进行成本实用性分析,具有代表无进展疾病,进展疾病和死亡的健康状态。使用质量调整的寿命(QALYS)测量健康效果,并在加拿大元表示成本。临床投入来自反映试验,使用参数生存模型外推外推。反映中收集的EQ-5D数据用于确定健康状态的实用价值观,并来自临床医生的调查,资源使用估计。模型预测增量成本为5,021美元,增量qalys为0.17,使Lenvatinib优于索拉非尼。该模型演示了Lenvatinib是加拿大在加拿大的高索拉非尼的资源使用,以治疗UHCC。与Sorafenib相比,总成本较低,而健康益处较大,分别在Lenvatinib ARM中延长了4.1和2.6个月的无进展和整体生存。

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