Cost-per-responder analysis of patients with lenalidomide-refractory multiple myeloma receiving ciltacabtagene autoleucel in CARTITUDE-4

被引:0
|
作者
Hansen, Doris K. [1 ]
Lu, Xiaoxiao [2 ]
Puglianini, Omar Castaneda [1 ]
Sorensen, Sonja [3 ]
Usmani, Saad Z. [4 ]
Zhang, Eileen [3 ]
Huo, Stephen [5 ]
Zhang, Yan [2 ]
Qureshi, Zaina P. [2 ]
Jagannath, Sundar [6 ]
机构
[1] H Lee Moffitt Canc Ctr & Res Inst, Dept Blood & Marrow Transplant & Cellular Immunoth, Tampa, FL 33612 USA
[2] Johnson & Johnson Co, Janssen Sci Affairs LLC, Horsham, PA USA
[3] Evidera, Bethesda, MD USA
[4] Mem Sloan Kettering Canc Ctr, New York, NY USA
[5] Janssen Global Serv LLC, Raritan, NJ USA
[6] Icahn Sch Med Mt Sinai, New York, NY USA
来源
FRONTIERS IN IMMUNOLOGY | 2024年 / 15卷
关键词
multiple myeloma; ciltacabtagene autoleucel; CAR T therapy; cost-per-responder analysis; cost-effectiveness analysis; daratumumab; pomalidomide; bortezomib; THERAPIES; OUTCOMES;
D O I
10.3389/fimmu.2024.1408892
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Introduction Ciltacabtagene autoleucel (cilta-cel) is a chimeric antigen receptor T-cell therapy approved for patients with relapsed/refractory multiple myeloma (RRMM). In the phase 3 trial, CARTITUDE-4 (NCT04181827), cilta-cel demonstrated improved efficacy vs. standard of care (SOC; daratumumab plus pomalidomide and dexamethasone [DPd] or pomalidomide plus bortezomib and dexamethasone [PVd]) with a >= complete response (>= CR) rate of 73.1% vs. 21.8%.Methods A cost-per-responder model was developed to assess the value of cilta-cel and SOC (87% DPd and 13% PVd) based on the CARTITUDE-4 trial data from a US mixed payer perspective (76.7% commercial, 23.3% Medicare). The model was developed using progression-free survival (PFS), overall survival (OS), and >= CR endpoints from CARTITUDE-4 over a period of 25.4 months. Inpatient stays, outpatient visits, drug acquisition, administration, and monitoring costs were included. The base-case model assumed an inpatient setting for each cilta-cel infusion; another scenario included 30% outpatient and 70% inpatient infusions. Costs of managing grade 3-4 adverse events (AEs) and grade 1-4 cytokine release syndrome and neurotoxicity were included. Subsequent therapy costs were incurred after disease progression; terminal care costs were considered upon death events. Outcomes included total cost per treated patient, total cost per complete responder, and cost per month in PFS between cilta-cel and SOC. Costs were adjusted to 2024 US dollars.Results Total cost per treated patient, total cost per complete responder, and total cost per month in PFS were estimated at $704,641, $963,941, and $30,978 for cilta-cel, respectively, and $840,730, $3,856,559, and $42,520 for SOC over the 25.4-month period. Cost drivers included treatment acquisition costs before progression and subsequent treatment costs ($451,318 and $111,637 for cilta-cel; $529,795 and $265,167 for SOC). A scenario analysis in which 30% of patients received an outpatient infusion (assuming the same payer mix) showed a lower cost per complete responder for cilta-cel ($956,523) than those with an infusion in the inpatient setting exclusively.Discussion This analysis estimated that cost per treated patient, cost per complete responder, and cost per month in PFS for cilta-cel were remarkably lower than for DPd or PVd, highlighting the substantial clinical and economic benefit of cilta-cel for patients with RRMM.
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