利用治疗序列模型估算抗 CD20 治疗复发性多发性硬化症的健康经济效益。

IF 2.5 Q2 CLINICAL NEUROLOGY Multiple Sclerosis Journal - Experimental, Translational and Clinical Pub Date : 2023-07-24 eCollection Date: 2023-07-01 DOI:10.1177/20552173231189398
Ide Smets, Matthijs Versteegh, Simone Huygens, Cato Corsten, Beatrijs Wokke, Joost Smolders
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引用次数: 0

摘要

背景:在高收入国家,有四种抗CD20单克隆抗体(mAbs)用于复发性多发性硬化症的治疗或正在研发中:奥克立珠单抗(ocrelizumab)、ofatumumab(均已注册)、乌利昔单抗(ublituximab)(正在等待注册)和利妥昔单抗(rituximab)(标签外)。注册药物和标签外药物的上市价格差异很大:从健康经济和社会角度比较抗CD20 mAbs之间的效益差异:为了反映 DMTs 的终生使用情况,我们使用了一个治疗序列模型,从健康(终生复发次数、达到扩展残疾状态量表 [EDSS] 6 的时间、终生质量调整生命年数)和成本效益(净健康效益)方面比较了 ocrelizumab/ofatumumab 和其他 8 类药物。为了与奥克立珠单抗相比更具成本效益,我们模拟了乌利昔单抗的上市价格和利妥昔单抗对 EDSS 进展的预期效果:尽管在一线和二线使用奥克立珠单抗的药物序列比奥妥木单抗更具成本效益,但我们的概率分析表明,这一结果非常不确定。要想比奥克利珠单抗更具成本效益,乌利昔单抗需要便宜约25%,而利妥昔单抗需要与一线治疗对残疾进展的影响相同:我们的模型显示,奥克雷珠单抗和奥妥木单抗的成本效益没有明显差异。因此,处方成本最低的抗 CD20 mAb 可以使多发性硬化症治疗民主化,而不会损失健康效益。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

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Health-economic benefits of anti-CD20 treatments in relapsing multiple sclerosis estimated using a treatment-sequence model.

Background: In high-income countries, four anti-CD20 monoclonal antibodies (mAbs) are used or in the pipeline for relapsing MS: ocrelizumab, ofatumumab (both registered), ublituximab (awaiting registration) and rituximab (off-label). List prices differ significantly between registered and off-label drugs.

Objective: Comparing differences in benefits between anti-CD20 mAbs from a health-economic and societal perspective.

Methods: To reflect lifetime use of DMTs, we used a treatment-sequence model to compare ocrelizumab/ofatumumab and eight other drug classes in terms of health (lifetime relapses, time to Expanded Disability Status Scale [EDSS] 6, lifetime quality-adjusted life years) and cost-effectiveness (net health benefit). To become cost-effective compared to ocrelizumab, we modelled the list price of ublituximab and desired effect on EDSS progression of rituximab.

Results: Although drug sequences with ocrelizumab in first- and second-line were more cost-effective than ofatumumab, our probabilistic analysis suggests this outcome was very uncertain. To be more cost-effective than ocrelizumab, ublituximab needs to be about 25% cheaper whilst rituximab needs to equal the effect on disability progression seen with first-line treatments.

Conclusions: Our model showed no clear difference in cost-effectiveness between ocrelizumab and ofatumumab. Hence, prescribing the least costly anti-CD20 mAb can democratise MS care without a loss in health benefits.

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来源期刊
CiteScore
4.70
自引率
0.00%
发文量
54
审稿时长
15 weeks
期刊最新文献
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