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在美国,对于三线或三线以上复发或难治性大 B 细胞淋巴瘤患者,利妥昔单抗注射用偶联物与阿基仑赛注射液和西达基奥仑赛注射液相比的成本效果分析。

Cost-Effectiveness of Lisocabtagene Maraleucel Versus Axicabtagene Ciloleucel and Tisagenlecleucel in the Third-Line or Later Treatment Setting for Relapsed or Refractory Large B-cell Lymphoma in the United States.

机构信息

Bristol Myers Squibb, Uxbridge, UK.

Bristol Myers Squibb, Princeton, NJ, USA.

出版信息

Adv Ther. 2023 May;40(5):2355-2374. doi: 10.1007/s12325-023-02444-x. Epub 2023 Mar 22.


DOI:10.1007/s12325-023-02444-x
PMID:36947328
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC10129927/
Abstract

INTRODUCTION: The objective of this study was to evaluate the cost-effectiveness of lisocabtagene maraleucel (liso-cel) versus other available chimeric antigen receptor T-cell therapies, including axicabtagene ciloleucel (axi-cel) and tisagenlecleucel (tisa-cel), in patients who had received at least two prior therapies from a United States (US) commercial third-party payer perspective. METHODS: To capture this heterogeneity in survival outcomes, we used mixture cure models to extrapolate progression-free survival (PFS) and overall survival (OS). Patient-level data from TRANSCEND NHL 001 for liso-cel and reconstructed patient-level data from ZUMA-1 for axi-cel, JULIET for tisa-cel, and SCHOLAR-1 for salvage chemotherapy, derived using the Guyot method, were used for OS and PFS. The model included adverse events associated with liso-cel, axi-cel, and tisa-cel. RESULTS: Liso-cel was less costly (incremental cost of - $74,980) and marginally more effective (0.002 incremental quality-adjusted life-years [QALY]) than axi-cel and had an incremental cost of $67,925 and 2.02 incremental QALYs over tisa-cel in the base case. Results remained consistent in sensitivity analyses, with the liso-cel OS cure fraction being the main driver of cost-effectiveness compared with both axi-cel and tisa-cel. CONCLUSION: This analysis estimated that liso-cel is cost-effective compared with tisa-cel and axi-cel from a commercial US payer perspective.

摘要

简介:本研究旨在从美国商业第三方支付者的角度评估 lisocabtagene maraleucel(liso-cel)与其他已上市嵌合抗原受体 T 细胞疗法(包括 axicabtagene ciloleucel [axi-cel] 和 tisagenlecleucel [tisa-cel])相比在至少接受过两次先前治疗的患者中的成本效益。

方法:为了捕捉生存结果的这种异质性,我们使用混合治愈模型推断无进展生存期(PFS)和总生存期(OS)。从 TRANSCEND NHL 001 中获得 liso-cel 的患者水平数据,从 ZUMA-1 中重建 axi-cel 的患者水平数据,从 JULIET 中获得 tisa-cel 的患者水平数据,从 SCHOLAR-1 中获得挽救性化疗的患者水平数据,使用 Guyot 方法,用于 OS 和 PFS。该模型包括与 liso-cel、axi-cel 和 tisa-cel 相关的不良事件。

结果:liso-cel 的成本更低(增量成本为-74980 美元),效果略高(0.002 个增量质量调整生命年[QALY]),与 axi-cel 相比,liso-cel 的增量成本为 67925 美元,与 tisa-cel 相比,增量 QALY 为 2.02。在敏感性分析中,结果保持一致,与 axi-cel 和 tisa-cel 相比,liso-cel 的 OS 治愈率是成本效益的主要驱动因素。

结论:从商业美国支付者的角度来看,这项分析估计 liso-cel 与 tisa-cel 和 axi-cel 相比具有成本效益。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1c93/10129927/1847d479fa07/12325_2023_2444_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1c93/10129927/6b7a305a3cb4/12325_2023_2444_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1c93/10129927/ef405ca9bc57/12325_2023_2444_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1c93/10129927/ac363d3ca42a/12325_2023_2444_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1c93/10129927/1847d479fa07/12325_2023_2444_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1c93/10129927/6b7a305a3cb4/12325_2023_2444_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1c93/10129927/ef405ca9bc57/12325_2023_2444_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1c93/10129927/ac363d3ca42a/12325_2023_2444_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1c93/10129927/1847d479fa07/12325_2023_2444_Fig4_HTML.jpg

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[4]
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Cost-effectiveness of second-line lisocabtagene maraleucel in relapsed or refractory diffuse large B-cell lymphoma.

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[6]
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本文引用的文献

[1]
Patterns of Use, Outcomes, and Resource Utilization among Recipients of Commercial Axicabtagene Ciloleucel and Tisagenlecleucel for Relapsed/Refractory Aggressive B Cell Lymphomas.

Transplant Cell Ther. 2022-10

[2]
Matching-adjusted indirect treatment comparison of chimeric antigen receptor T-cell therapies for third-line or later treatment of relapsed or refractory large B-cell lymphoma: lisocabtagene maraleucel versus tisagenlecleucel.

Exp Hematol Oncol. 2022-3-25

[3]
Health State Utilities for Adverse Events Associated with Chimeric Antigen Receptor T-Cell Therapy in Large B-Cell Lymphoma.

Pharmacoecon Open. 2022-5

[4]
Long-term clinical outcomes of tisagenlecleucel in patients with relapsed or refractory aggressive B-cell lymphomas (JULIET): a multicentre, open-label, single-arm, phase 2 study.

Lancet Oncol. 2021-10

[5]
Matching-adjusted indirect treatment comparison of liso-cel versus axi-cel in relapsed or refractory large B cell lymphoma.

J Hematol Oncol. 2021-9-8

[6]
Comparison of 2-year outcomes with CAR T cells (ZUMA-1) vs salvage chemotherapy in refractory large B-cell lymphoma.

Blood Adv. 2021-10-26

[7]
Improving outcomes and mitigating costs associated with CAR T-cell therapy.

Am J Manag Care. 2021-8

[8]
Cost-Effectiveness Analysis of Tisagenlecleucel for the Treatment of Patients With Relapsed or Refractory Diffuse Large B-Cell Lymphoma in the United States.

Clin Ther. 2021-8

[9]
Efficacy and safety of CD19-directed CAR-T cell therapies in patients with relapsed/refractory aggressive B-cell lymphomas: Observations from the JULIET, ZUMA-1, and TRANSCEND trials.

Am J Hematol. 2021-10-1

[10]
Indirect Treatment Comparison of Liso-Cel vs. Salvage Chemotherapy in Diffuse Large B-Cell Lymphoma: TRANSCEND vs. SCHOLAR-1.

Adv Ther. 2021-6

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