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


Authors: Hansen, D. K.; Lu, X.; Puglianini, O. C.; Sorensen, S.; Usmani, S. Z.; Zhang, E.; Huo, S.; Zhang, Y.; Qureshi, Z. P.; Jagannath, S.
Article Title: Cost-per-responder analysis of patients with lenalidomide-refractory multiple myeloma receiving ciltacabtagene autoleucel in CARTITUDE-4
Abstract: 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. Copyright © 2024 Hansen, Lu, Puglianini, Sorensen, Usmani, Zhang, Huo, Zhang, Qureshi and Jagannath.
Keywords: treatment outcome; aged; middle aged; lenalidomide; thalidomide; clinical trial; mortality; antineoplastic agent; progression free survival; bortezomib; multiple myeloma; antineoplastic combined chemotherapy protocols; dexamethasone; drug resistance; drug resistance, neoplasm; monoclonal antibody; economics; immunology; antibodies, monoclonal; chimeric antigen receptor; phase 3 clinical trial; drug therapy; cost-effectiveness analysis; cost-benefit analysis; therapy; adoptive immunotherapy; immunotherapy, adoptive; cost benefit analysis; progression-free survival; adverse event; procedures; pomalidomide; humans; human; male; female; daratumumab; receptors, chimeric antigen; ciltacabtagene autoleucel; car t therapy; cost-per-responder analysis
Journal Title: Frontiers in Immunology
Volume: 15
ISSN: 1664-3224
Publisher: Frontiers Media S.A.  
Date Published: 2024-08-21
Start Page: 1408892
Language: English
DOI: 10.3389/fimmu.2024.1408892
PUBMED: 39234256
PROVIDER: scopus
PMCID: PMC11372240
DOI/URL:
Notes: Article -- Source: Scopus
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  1. Saad Zafar Usmani
    297 Usmani