Cost-Effectiveness Analysis of Adding Daratumumab to Bortezomib, Melphalan, and Prednisone for Untreated Multiple Myeloma

被引:7
作者
Cao, Yaohua [1 ]
Zhao, Lina [2 ]
Zhang, Tiantian [2 ,3 ]
Cao, Weiling [1 ]
机构
[1] Shenzhen Univ, Affiliated Luohu Hosp, Affiliated Hosp 3, Dept Pharm, Shenzhen, Peoples R China
[2] Jinan Univ, Coll Pharm, Guangzhou, Peoples R China
[3] Guangzhou Huabo Biopharmaceut Res Inst, Guangzhou, Peoples R China
关键词
Markov; cost-effectiveness; daratumumab; multiple myeloma; not eligible for stem cell transplantation;
D O I
10.3389/fphar.2021.608685
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Background: To evaluate the cost-effectiveness of adding daratumumab to bortezomib, melphalan, and prednisone for transplant-ineligible newly diagnosed multiple myeloma patients. Methods: A three-state Markov model was developed from the perspective of US payers to simulate the disease development of patient's life time for daratumumab plus bortezomib, melphalan, and prednisone (D-VMP) and bortezomib, melphalan, and prednisone (VMP) regimens. The primary outputs were total costs, expected life-years (LYs), quality-adjusted life-years (QALYs) and incremental cost-effectiveness ratios (ICERs). Results: The base case results showed that adding daratumumab to VMP provided an additional 3.00 Lys or 2.03 QALYs, at a cost of $262,526 per LY or $388,364 per QALY. Sensitivity analysis indicated that the results were most sensitive to utility of progression disease of D-VMP regimens, but no matter how these parameters changed, ICERs remained higher than $150,000 per QALY. Conclusion: In the case that the upper limit of willingness to pay threshold was $150,000 per QALY from the perspective of US payers, D-VMP was not a cost-effective regimen compared to VMP.
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页数:7
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