The cost-effectiveness of new first-line therapies approved in advanced hepatocellular carcinoma

伦瓦提尼 医学 阿替唑单抗 贝伐单抗 肝细胞癌 肿瘤科 索拉非尼 内科学 随机对照试验 无进展生存期 成本效益 无容量 总体生存率 癌症 免疫疗法 化疗 风险分析(工程)
作者
Jacopo Giuliani,Beatrice Mantoan,Andrea Bonetti
出处
期刊:Journal of Oncology Pharmacy Practice [SAGE]
卷期号:28 (2): 434-437 被引量:5
标识
DOI:10.1177/10781552211045013
摘要

The introduction of targeted agents (lenvatinib) and immune-based therapies (atezolizumab in combination with bevacizumab) for first-line advanced hepatocellular carcinoma provided new therapeutic options. The aim of this paper was to assess the cost-effectiveness of lenvatinib and the combination of atezolizumab plus bevacizumab in first-line for advanced hepatocellular carcinoma. Pivotal phase III randomized controlled trials were considered. Incremental cost-effectiveness ratio was calculated as the ratio between the difference of the costs in the intervention and in the control groups (pharmacy costs) and the difference between the effect in the intervention and in the control groups (progression free survival). One thousand four hundred and fifty five patients were included. The lowest cost for month of progression free survival-gain was associated with lenvatinib, with 139.24 € per month progression free survival-gained. Combining pharmacological costs of drugs with the measure of efficacy represented by progression free survival, lenvatinib is a cost-effective treatment in first-line for advanced hepatocellular carcinoma.
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