在加拿大,使用嵌合抗原受体t细胞治疗的患者的实际医疗保健费用。

IF 2.2 4区 医学 Q3 HEMATOLOGY
Lisa Masucci, John Kuruvilla, Beate Sander, Anca Prica, William W L Wong, Kelvin K W Chan
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引用次数: 0

摘要

嵌合抗原受体t细胞(CAR-T)疗法是一种改变实践的高成本疗法;然而,人们对CAR-T的实际成本知之甚少。我们估计了与CAR-T疗法相关的急性DLBCL患者的医疗费用。我们对2020年1月1日至2021年8月31日在安大略省多伦多玛格丽特公主癌症中心接受CAR-T治疗的患者进行了一项回顾性队列研究。成本被划分为不同的成本计算阶段。计算每个阶段和服务类别的平均总成本。53名患者接受了CAR-T治疗。平均年龄61岁,男性居多(60%)。每位患者的总平均成本为:预处理阶段(30天)为11,180加元(95% CI: 7712-14,649加元),治疗阶段为511,983加元(平均产品成本473,127加元)(95% CI: 504,472-520,666加元),治疗后阶段(100天)为41,620加元(95% CI: 29,935-52,933加元)。这些成本信息可以为CAR-T的成本效益分析以及报销决策提供信息。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Real-world healthcare costs for patients treated with chimeric antigen receptor T-cell therapy in Canada.

Chimeric antigen receptor T-cell (CAR-T) therapy is a practice changing high-cost therapy; however, little is known about the real-world cost of CAR-T. We estimated the acute healthcare costs associated with CAR-T for patients with r/r DLBCL. We performed a retrospective cohort study of patients who received CAR-T between 1 January 2020 and 31 August 2021 at Princess Margaret Cancer Center, Toronto, Ontario. Costs were divided into distinct costing phases. Mean total costs per phase and by service category were calculated. Fifty-three patients received CAR-T. The mean age was 61 years and the majority were male (60%). The total mean costs per patient were: C$11,180 (95% CI: $7712-14,649) for the pretreatment phase (30 days), C$511,983 (average product cost C$473,127) (95% CI: $504,472-520,666) for the treatment phase, and C$41,620 (95% CI: $29,935-52,933) for the post-treatment phase (100 days). This cost information may inform cost-effectiveness analyses for CAR-T as well as reimbursement decisions.

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来源期刊
Leukemia & Lymphoma
Leukemia & Lymphoma 医学-血液学
CiteScore
4.10
自引率
3.80%
发文量
384
审稿时长
1.8 months
期刊介绍: Leukemia & Lymphoma in its fourth decade continues to provide an international forum for publication of high quality clinical, translational, and basic science research, and original observations relating to all aspects of hematological malignancies. The scope ranges from clinical and clinico-pathological investigations to fundamental research in disease biology, mechanisms of action of novel agents, development of combination chemotherapy, pharmacology and pharmacogenomics as well as ethics and epidemiology. Submissions of unique clinical observations or confirmatory studies are considered and published as Letters to the Editor
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