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曲妥珠单抗-德拉昔替尼用于美国 HER2 低表达晚期乳腺癌的成本效果分析。

Cost-effectiveness of Trastuzumab Deruxtecan for HER2-low Advanced Breast Cancer in the United States.

机构信息

Department of Pharmacy, the Second Xiangya Hospital of Central South University, Changsha, China; Institute of Clinical Pharmacy, Central South University, Changsha, China.

Department of Pharmacy, the Second Xiangya Hospital of Central South University, Changsha, China.

出版信息

Clin Ther. 2023 Oct;45(10):965-972. doi: 10.1016/j.clinthera.2023.07.014. Epub 2023 Aug 1.

Abstract

PURPOSE

Trastuzumab deruxtecan has been shown to be effective for advanced breast cancer with low levels of human epidermal growth factor receptor 2. To optimize the allocation of limited health care resources, this study evaluated the cost-effectiveness of trastuzumab deruxtecan from the US payer perspective.

METHODS

A partitioned survival model was developed to project the disease course of advanced breast cancer. Clinical efficacy, treatment utilization, safety, and cost data were gathered from the DESTINY-Breast04 (Trastuzumab Deruxtecan in Previously Treated HER2-Low Advanced Breast Cancer) trial and the Centers for Medicare & Medicaid Services. Transition probabilities were obtained from the reported survival probabilities per DESTINY-Breast04 group. The incremental cost-effectiveness ratio (ICER), the incremental monetary benefit, and the incremental net health benefit were measured. One-way sensitivity analysis, probabilistic sensitivity analysis, and subgroup analysis were performed to explore the uncertainty of the model.

FINDINGS

Trastuzumab deruxtecan had an ICER of $307,751 per quality-adjusted life-year (QALY) gained, with an incremental net health benefit of -0.317 QALY and an incremental monetary benefit of -$63,313 compared with the physician's choice of alternative chemotherapy agents. Subgroup analysis indicated that trastuzumab deruxtecan had an ICER of $383,776 per QALY gained for the hormone receptor-positive subgroup and an ICER of $194,424 per QALY for the hormone receptor-negative subgroup. One-way sensitivity analysis showed that the cost of trastuzumab deruxtecan had the most impact on model outcomes. The cost-effectiveness acceptability curve projected that the probability of trastuzumab deruxtecan being cost-effective was 5% in the overall population, 2% in the hormone receptor-positive subgroup, and 56% in the hormone receptor-negative subgroup at the willingness-to-pay threshold of $200,000 per QALY.

IMPLICATIONS

Trastuzumab deruxtecan may be a cost-effective option for hormone receptor-negative patients with advanced breast cancer with low levels of human epidermal growth factor receptor 2.

摘要

目的

曲妥珠单抗-德鲁替康已被证明对人表皮生长因子受体 2 水平较低的晚期乳腺癌有效。为了优化有限医疗保健资源的分配,本研究从美国支付者的角度评估了曲妥珠单抗-德鲁替康的成本效益。

方法

建立了一个分区生存模型来预测晚期乳腺癌的疾病进程。临床疗效、治疗利用、安全性和成本数据来自 DESTINY-Breast04(曲妥珠单抗-德鲁替康治疗先前治疗的 HER2 低水平晚期乳腺癌)试验和医疗保险和医疗补助服务中心。转移概率是根据每个 DESTINY-Breast04 组报告的生存概率获得的。测量了增量成本效益比(ICER)、增量货币收益和增量净健康收益。进行了单因素敏感性分析、概率敏感性分析和亚组分析,以探讨模型的不确定性。

结果

与医生选择的替代化疗药物相比,曲妥珠单抗-德鲁替康每获得 1 个质量调整生命年(QALY)的增量成本效益比为 307751 美元,增量净健康效益为-0.317 QALY,增量货币效益为-63313 美元。亚组分析表明,曲妥珠单抗-德鲁替康在激素受体阳性亚组的每 QALY 增量成本效益比为 383776 美元,在激素受体阴性亚组的每 QALY 增量成本效益比为 194424 美元。单因素敏感性分析表明,曲妥珠单抗-德鲁替康的成本对模型结果的影响最大。成本效益接受曲线预测,在支付意愿阈值为每 QALY200000 美元时,曲妥珠单抗-德鲁替康在总体人群中的成本效益可能性为 5%,在激素受体阳性亚组中的成本效益可能性为 2%,在激素受体阴性亚组中的成本效益可能性为 56%。

结论

对于人表皮生长因子受体 2 水平较低的激素受体阴性晚期乳腺癌患者,曲妥珠单抗-德鲁替康可能是一种具有成本效益的选择。

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