奥拉帕尼
医学
肿瘤科
内科学
前列腺
前列腺癌
癌症
基因
生物
聚ADP核糖聚合酶
遗传学
聚合酶
作者
Yiyuan Li,Shen Lin,Lixian Zhong,Shaohong Luo,Xiaoting Huang,Xiaojia Huang,Liangliang Dong,Xiongwei Xu,Xiuhua Weng
出处
期刊:Pharmacogenomics
[Future Medicine]
日期:2021-08-01
卷期号:22 (13): 809-819
被引量:8
标识
DOI:10.2217/pgs-2021-0061
摘要
Aim: To compare the cost–effectiveness of olaparib versus control treatment in metastatic castration-resistant prostate cancer patients with at least one gene mutation in BRCA1, BRCA2 or ATM from the US payer perspective. Methods: A Markov model was constructed to assess the quality-adjusted life years (QALYs) and incremental cost–effectiveness ratios. Sensitivity analyses and scenario analyses were conducted to explore the impact of uncertainties. Results: The base-case result indicated that, for patients with specific gene mutations, olaparib gained 1.26 QALYs and USD$157,732 total cost. Compared with control treatment, the incremental cost–effectiveness ratio of olaparib was USD$248,248/QALY. The price of olaparib was the most influential parameter. Conclusion: Olaparib is not cost effective in comparison with control treatment in metastatic castration-resistant prostate cancer patients with specific gene mutations.
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