BluePath Solutions, Los Angeles, CA, USA.
Bristol Myers Squibb, Princeton, NJ, USA.
Adv Ther. 2023 Oct;40(10):4626-4638. doi: 10.1007/s12325-023-02623-w. Epub 2023 Aug 19.
Patients with triple-class exposed relapsed/refractory multiple myeloma (RRMM) have poor outcomes with substantial healthcare costs. Idecabtagene vicleucel (ide-cel), a B-cell maturation antigen (BCMA)-directed chimeric antigen receptor (CAR) T cell therapy, showed deep, durable responses in patients with RRMM in the pivotal phase 2 KarMMa trial (NCT03361748). Healthcare resource utilization (HCRU) and costs were estimated for ide-cel-treated patients in the KarMMa trial.
Post-infusion costs were estimated based on HCRU data, including facility care, diagnostics, medications, and procedures. Length of stay (LOS) was extracted for inpatient and intensive care unit (ICU) care. All patients had a 14-day post-infusion inpatient stay per trial protocol. Analyses were conducted for patients treated in the United States (US), who received the ide-cel target dose of 450 × 10 CAR + T cells and assuming a 7-day inpatient stay.
Overall, 128 patients received ide-cel and were included in this analysis. Mean age was 60 years, 59% were men, and 81% were white. Mean total LOS was 23.9 days. Total estimated costs over 24 months post-infusion were US$115,614 per patient, driven by facility costs (75%; $86,385). Most costs were incurred in the first month (58%; $67,259). The scenario analysis assuming a 7-day inpatient stay showed estimated 24-month costs of $92,294. For the 54 (42%) patients who received ide-cel high dose, total costs over 24 months were $113,298 per patient.
Extrapolation of costs based on HCRU data from patients receiving single-infusion of ide-cel in the KarMMa trial showed substantially reduced HCRU and costs over 2 years after initial treatment. Most costs were incurred during the first month after ide-cel infusion, likely attributable to the 14-day inpatient stay required by the trial protocol. These findings suggest a nominal, incremental monthly cost of care immediately after treatment, which may be lower in routine clinical practice.
接受过三药联合治疗后复发/难治性多发性骨髓瘤(RRMM)的患者预后较差,医疗费用巨大。Idecabtagene vicleucel(ide-cel)是一种 B 细胞成熟抗原(BCMA)导向的嵌合抗原受体(CAR)T 细胞疗法,在关键性 2 期 KarMMa 试验(NCT03361748)中,接受 ide-cel 治疗的 RRMM 患者显示出深度和持久的缓解。
根据 KarMMa 试验中的 HCRU 数据,包括设施护理、诊断、药物和程序,估算 ide-cel 治疗患者的医疗资源利用(HCRU)和成本。提取住院和重症监护病房(ICU)护理的住院时间(LOS)。根据试验方案,所有患者在输注后 14 天内住院。分析在美国(US)接受 ide-cel 目标剂量为 450×10 CAR+T 细胞治疗的患者。
共有 128 例患者接受 ide-cel 治疗并纳入该分析。平均年龄为 60 岁,59%为男性,81%为白人。平均总 LOS 为 23.9 天。输注后 24 个月的总估计成本为每位患者 115614 美元,主要由设施成本(75%;86385 美元)驱动。大多数费用发生在第一个月(58%;67259 美元)。假设住院 7 天的情景分析显示,估计在 24 个月内每位患者的成本为 92294 美元。对于接受 ide-cel 高剂量的 54 例(42%)患者,输注后 24 个月的总费用为每位患者 113298 美元。
基于 KarMMa 试验中单次输注 ide-cel 患者的 HCRU 数据进行成本推断显示,在初始治疗后 2 年内,HCRU 和成本大幅降低。大多数费用发生在 ide-cel 输注后的第一个月,可能归因于试验方案要求的 14 天住院。这些发现表明,治疗后立即产生一个名义上的、增量的每月护理费用,在常规临床实践中可能更低。