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曲妥珠单抗-德鲁替康与曲妥珠单抗-美坦新在中国人群 HER2 阳性转移性乳腺癌中的成本-效用分析。

Cost-utility analysis of trastuzumab deruxtecan versus trastuzumab emtansine in HER2-positive metastatic breast cancer in Chinese setting.

机构信息

Department of Clinical Pharmacy, Shanghai General Hospital, Shanghai Jiao Tong University School of Medicine, Shanghai, 200080, China.

Department of Pharmacy, The First Affiliated Hospital of Wannan Medical College, Anhui, China.

出版信息

J Cancer Res Clin Oncol. 2023 Dec;149(20):17933-17942. doi: 10.1007/s00432-023-05496-2. Epub 2023 Nov 14.

DOI:10.1007/s00432-023-05496-2
PMID:37964082
Abstract

PURPOSE

Trastuzumab deruxtecan (T-DXd) expressed substantial improvement in the progression-free survival and overall survival contrasted with trastuzumab emtansine (T-DM1) in patients with HER2-positive metastatic breast cancer (mBC), becoming the second-line standard of care, promisingly. We aim to estimate the cost-utility of T-DXd versus T-DM1 in HER2-positive mBC from the Chinese healthcare perspective.

METHODS

A partitioned survival model was applied to examine the cost-utility of T-DXd versus T-DM1. Clinical patients and outcome data were sourced from the DESTINY-Breast 03 trial. Costs and utilities were sourced in Chinese setting. Total costs, quality-adjusted life months (QALMs), and an incremental cost-utility ratios (ICUR) were calculated for cost-utility analysis. The willingness-to-pay threshold was set at $3188/QALM. Univariate, scenario, and probabilistic sensitivity analyses were performed.

RESULTS

T-DXd group gained ∆QALM of 7.09 months and ∆Cost of $304,503 compared with T-DM1 therapy, which caused an ICUR of $42,936/QALM. The results of sensitivity analyses confirmed the base-case findings. Furthermore, T-DXd must reduce the price to enter the Chinese mainland market. At least when the cycle cost of T-DXd is reduced to $2975, T-DXd has an 83.3% chance of becoming a better choice.

CONCLUSIONS

T-DXd appears to be not cost effective compared with T-DM1 for HER2-positive mBC patients previously treated with trastuzumab and a taxane.

摘要

目的

曲妥珠单抗-德鲁替康(T-DXd)在 HER2 阳性转移性乳腺癌(mBC)患者中的无进展生存期和总生存期与曲妥珠单抗-美坦新偶联物(T-DM1)相比有显著改善,成为二线治疗标准,前景看好。我们旨在从中国医疗保健角度评估 T-DXd 对比 T-DM1 在 HER2 阳性 mBC 中的成本效用。

方法

采用分割生存模型评估 T-DXd 对比 T-DM1 的成本效用。临床患者和结局数据来源于 DESTINY-Breast 03 试验。成本和效用数据来源于中国情境。计算成本效用分析的总费用、质量调整生命月(QALM)和增量成本效用比(ICUR)。意愿支付阈值设定为 3188 美元/QALM。进行了单变量、情景和概率敏感性分析。

结果

与 T-DM1 治疗相比,T-DXd 组获得了 7.09 个月的 QALM 增益和 304503 美元的增量成本,导致 ICUR 为 42936 美元/QALM。敏感性分析的结果证实了基础案例的发现。此外,T-DXd 必须降低价格才能进入中国大陆市场。至少当 T-DXd 的周期成本降低到 2975 美元时,T-DXd 才有 83.3%的可能性成为更好的选择。

结论

与先前接受曲妥珠单抗和紫杉烷治疗的 HER2 阳性 mBC 患者相比,T-DXd 用于治疗 HER2 阳性 mBC 似乎不具有成本效益。

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