Department of Pharmacy, Huangpu Branch, Shanghai Ninth People's Hospital, Shanghai Jiao Tong University School of Medicine, No.58 Puyu East Road, Huangpu District, Shanghai, 200011, China.
Department of Pharmacy, Huangpu Branch, Shanghai Ninth People's Hospital, Shanghai Jiao Tong University School of Medicine, No.58 Puyu East Road, Huangpu District, Shanghai, 200011, China.
Breast. 2023 Apr;68:173-180. doi: 10.1016/j.breast.2023.02.003. Epub 2023 Feb 10.
The ASCENT trial demonstrated the efficacy of sacituzumab govitecan for the treatment of advanced or metastatic triple-negative breast cancer (TNBC). The current study evaluated the cost-effectiveness of receiving sacituzumab govitecan compared with standard of care chemotherapy from the United States payer perspective.
A partitioned survival approach was used to project the disease course of advanced or metastatic TNBC. Two survival modes were applied to analyze two groups of patients. The survival data were gathered from the ASCENT trial. Direct medical costs were derived from the data of Centers for Medicare & Medicaid Services. Utility data was collected from the published literature. The incremental cost-utility ratio (ICUR) was the primary outcome that measured the cost-effectiveness of therapy regimen. One-way sensitivity and probabilistic sensitivity analysis were implemented to explore the uncertainty and validate the stability of results.
In the base-case, the ICUR of sacituzumab govitecan versus chemotherapy is $ 778,771.9/QALY and $ 702,281/QALY for full population group and brain metastatic-negative (BMN) group with the setting of classic survival mode. And in the setting of cure survival mode, the ICUR is $ 506,504.5/QALY for the full population group and $ 274,232.0/QALY for BMN population group. One-way sensitivity analyses revealed that the unit cost of sacituzumab govitecan and body weight were key roles that lower the ICUR value. Probabilistic sensitivity analyses also showed that reducing the unit price of sacituzumab govitecan can improve the likelihood of becoming cost-effective.
The cost-effectiveness analysis suggested that from a US payer perspective, sacituzumab govitecan at current price is unlikely to be a preferred option for patients with advanced or metastatic TNBC at a threshold of $ 150,000/QALY.
ASCENT 试验证明了 sacituzumab govitecan 治疗晚期或转移性三阴性乳腺癌(TNBC)的疗效。本研究从美国支付者的角度评估了接受 sacituzumab govitecan 治疗与标准护理化疗相比的成本效益。
采用分区生存方法来预测晚期或转移性 TNBC 的疾病进程。应用两种生存模式来分析两组患者。生存数据来自 ASCENT 试验。直接医疗成本来自医疗保险和医疗补助服务中心的数据。效用数据来自已发表的文献。增量成本效益比(ICUR)是衡量治疗方案成本效益的主要指标。进行了单因素敏感性分析和概率敏感性分析,以探讨不确定性并验证结果的稳定性。
在基础情况下,sacituzumab govitecan 与化疗相比,在经典生存模式下,全人群组和无脑转移阴性(BMN)组的 ICUR 分别为$778,771.9/QALY 和$702,281/QALY。在治愈生存模式下,全人群组的 ICUR 为$506,504.5/QALY,BMN 人群组的 ICUR 为$274,232.0/QALY。单因素敏感性分析表明,sacituzumab govitecan 的单位成本和体重是降低 ICUR 值的关键因素。概率敏感性分析还表明,降低 sacituzumab govitecan 的单位价格可以提高其成为成本效益的可能性。
从美国支付者的角度来看,在 150,000 美元/QALY 的阈值下,考虑到当前价格,sacituzumab govitecan 不太可能成为晚期或转移性 TNBC 患者的首选治疗方案。