A Cost-Effectiveness Analysis of Axicabtagene Ciloleucel versus Tisagenlecleucel in the Treatment of Diffuse Large B-cell Lymphoma Based on a Real-World French Registry

被引:0
作者
Ray, Markqayne [1 ]
Castaigne, Jean-Gabriel [2 ]
Zang, Alexandra [3 ]
Patel, Anik [1 ]
Hancock, Elizabeth [4 ]
Brighton, Nicholas [4 ]
Bachy, Emmanuel [5 ,6 ]
机构
[1] Kite, Gilead Co, Santa Monica, CA 90404 USA
[2] Kite, Gilead Co, London, England
[3] Kite, Gilead Co, Paris, France
[4] Source Hlth Econ, London, England
[5] Hosp Civils Lyon, Haematol Dept, Lyon, Pierre Benite, France
[6] Inserm, U1111, Int Ctr Infectiol Res CIRI, Lyon, France
关键词
Real-world data; Cost-effectiveness analysis; Diffuse large B-cell lymphoma; CAR-T therapy; OUTCOMES; TRANSPLANTATION; CHEMOTHERAPY; REMISSIONS;
D O I
10.1007/s12325-024-02971-1
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
IntroductionAxicabtagene ciloleucel (axi-cel) and tisagenlecleucel (tisa-cel) are chimeric antigen receptor T-cell therapies that were evaluated in third and later line (3L+) relapsed or refractory (r/r) diffuse large B-cell lymphoma (DLBCL) in the ZUMA-1 and JULIET trials, respectively. As of October 2021, the DESCAR-T registry included 729 French patients with 3L+ r/r DLBCL who received axi-cel or tisa-cel. Using these data, propensity score matching was used to conduct an adjusted comparison between axi-cel and tisa-cel. Axi-cel was associated with statistically significant improvements in overall survival (OS) and progression-free survival (PFS), and significantly more frequent Grade >= 3 immune effector cell-associated neurotoxicity syndrome (ICANS), compared with tisa-cel. There was no significant difference in Grade >= 3 cytokine release syndrome (CRS). The current analysis assessed the cost-effectiveness of axi-cel versus tisa-cel in the treatment of 3L+ r/r DLBCL using propensity score-matched data from the DESCAR-T registry.MethodsA partitioned survival model was used to extrapolate costs and quality-adjusted life years (QALYs) over a lifetime. Survival curves for PFS and OS were based on independent mixture cure models fitted to digitized Kaplan-Meier data for the propensity score-matched DESCAR-T populations. Average duration of intensive care unit stays for each of axi-cel and tisa-cel in DESCAR-T were used to inform adverse event costs. Selected parametric survival distributions were based on clinical expert validation. Utility values were derived from ZUMA-1, and costs were obtained from French registries and published sources. List prices were used for both axi-cel and tisa-cel. Costs and outcomes were discounted at an annual rate of 2.5%.ResultsAxi-cel is associated with an incremental cost-effectiveness ratio of <euro>15,520 per QALY compared with tisa-cel.ConclusionBased on explicit willingness-to-pay thresholds applied in Europe, axi-cel is expected to be a cost-effective use of healthcare resources in real-world clinical settings compared with tisa-cel in 3L+ r/r DLBCL.
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收藏
页码:4282 / 4298
页数:17
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