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聚(ADP-核糖)聚合酶(PARP)抑制剂奥拉帕利在中国和美国转移性去势抵抗性前列腺癌患者中的成本效益

Cost-effectiveness of olaparib, a PARP inhibitor, for patients with metastatic castration-resistant prostate cancer in China and United States.

作者信息

Xu Chenxia, Cai Jiaqin, Zhuang Jie, Zheng Bin, Chen Li, Sun Hong, Zheng Guiyan, Wei Xiaoxia, Liu Maobai

机构信息

Department of Pharmacy, Fujian Medical University Union Hospital, Fuzhou, China.

The School of Pharmacy, Fujian Medical University, Fuzhou, China.

出版信息

Ann Transl Med. 2022 Aug;10(15):830. doi: 10.21037/atm-22-3637.

Abstract

BACKGROUND

Metastatic prostate cancer is initially sensitive to androgen receptor inhibition, but eventually becomes metastatic castration-resistant prostate cancer (mCRPC). Olaparib has longer progression-free survival and better measures of response and patient-reported end points than either enzalutamide or abiraterone. In the present study, 2 Markov models were established to analyze the cost utility of olaparib in treating mCRPC from the perspectives of health services in China and the United States.

METHODS

Markov models were established to simulate the progress of mCRPC in China and the United States. The state transition probabilities and clinical data were extracted from the PROfound trial. The cost data were estimated from local pricing, the relevant literature and expert consultancy. The health outcomes are expressed by quality-adjusted life years (QALYs). All costs and incremental cost-effectiveness ratios (ICERs) are presented in US dollars. One-way deterministic sensitivity analysis and probabilistic sensitivity analysis were performed to assess the uncertainty of the models.

RESULTS

Based on the Chinese Markov model, the base case ICER for olaparib versus the control group was ¥392,727.87, with incremental costs of ¥93,673.23 and an incremental QALY of 0.23, indicating that it was not cost effective from the aspect of the Chinese healthcare system. However, as shown by the American Markov model, olaparib was dominant versus the control group, with a cost saving of $69,675.20 and a gain of 0.23 QALYs. One-way deterministic sensitivity analysis and probabilistic sensitivity analyses showed that the modeling results were not significantly affected by the model parameters.

CONCLUSIONS

Olaparib treatment in patients with mCRPC is not cost effective in China, but it is cost saving in the United States.

摘要

背景

转移性前列腺癌最初对雄激素受体抑制敏感,但最终会发展为去势抵抗性前列腺癌(mCRPC)。与恩杂鲁胺或阿比特龙相比,奥拉帕利具有更长的无进展生存期,以及更好的缓解指标和患者报告的终点指标。在本研究中,建立了2个马尔可夫模型,从中国和美国卫生服务的角度分析奥拉帕利治疗mCRPC的成本效益。

方法

建立马尔可夫模型以模拟中国和美国mCRPC的进展。状态转移概率和临床数据取自PROfound试验。成本数据根据当地定价、相关文献和专家咨询估算得出。健康结果用质量调整生命年(QALY)表示。所有成本和增量成本效益比(ICER)均以美元为单位呈现。进行单向确定性敏感性分析和概率敏感性分析以评估模型的不确定性。

结果

基于中国的马尔可夫模型,奥拉帕利与对照组相比的基础病例ICER为392,727.87元,增量成本为93,673.23元,增量QALY为0.23,这表明从中国医疗保健系统的角度来看,其不具有成本效益。然而,如美国马尔可夫模型所示,奥拉帕利相对于对照组具有优势,节省成本69,675.20美元,QALY增加0.23。单向确定性敏感性分析和概率敏感性分析表明,模型结果未受到模型参数的显著影响。

结论

奥拉帕利治疗mCRPC患者在中国不具有成本效益,但在美国具有成本节约效益。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/79a4/9403933/6102199a5dc4/atm-10-15-830-f1.jpg

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