芬戈莫德与干扰素β 1-a:基于TRANSFORMS个体患者数据的利弊评估方法。

IF 2.5 Q2 CLINICAL NEUROLOGY
Alessandra Spanu, Hélène E Aschmann, Jürg Kesselring, Milo A Puhan
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引用次数: 0

摘要

背景:Fingolimod是一种被批准用于多发性硬化症的疾病改善药物,但与其他积极治疗相比,其利弊平衡从未被评估过。目的:我们的目的是通过评估可注射干扰素与FTY720口服干扰素在RRMS试验中的个体患者数据,比较fingolimod与干扰素β -1a的益处和危害。方法:我们对患者的健康状况进行建模,包括扩展残疾状态量表测量、复发和任何不良事件。我们使用预先设定的最小重要差值4.6,评估各组之间的平均健康状况以及健康状况相对于基线恶化或改善的患者比例。我们进行了敏感性分析来检验我们的假设。结果:主分析和敏感性分析表明芬戈莫德0.5 mg优于干扰素β -1a。平均健康状况差异为1.01 (95% CI 0.93-1.08)。服用fingolimod 0.5 mg的患者为0.47 (95% CI: 0.35-0.63, p)。结论:在1年内,fingolimod相对于干扰素β -1a的净获益未达到临床相关性,但从长期来看,健康状况恶化的风险降低可能更为明显,患者可能更倾向于使用fingolimod减轻治疗负担。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Fingolimod versus interferon beta 1-a: Benefit-harm assessment approach based on TRANSFORMS individual patient data.

Fingolimod versus interferon beta 1-a: Benefit-harm assessment approach based on TRANSFORMS individual patient data.

Fingolimod versus interferon beta 1-a: Benefit-harm assessment approach based on TRANSFORMS individual patient data.

Fingolimod versus interferon beta 1-a: Benefit-harm assessment approach based on TRANSFORMS individual patient data.

Background: Fingolimod is a disease-modifying drug approved for multiple sclerosis but its benefit-harm balance has never been assessed compared to other active treatments.

Objectives: Our aim was to compare the benefits and harms of fingolimod with interferon beta-1a using individual patient data from TRial Assessing injectable interferon versus FTY720 Oral in RRMS trial.

Methods: We modelled the health status of patients over time including Expanded Disability Status Scale measurements, relapses and any adverse events. We assessed the mean health status between arms and the proportion of patients whose health deteriorated or improved relatively to baseline, using a prespecified minimal important difference of 4.6. We performed sensitivity analyses to test our assumptions.

Results: Main and sensitivity analyses favoured fingolimod 0.5 mg over interferon beta-1a. The average health status difference was 1.01 (95% CI 0.93-1.08). Patients on fingolimod 0.5 mg were 0.47 (95% CI: 0.35-0.63, p < 0.001) times less likely to experience a relevant decline in health status compared to interferon beta-1a patients, with a number needed to treat of 7.10 [5.18, 11.23].

Conclusions: Fingolimod's net benefit over interferon beta-1a did not reach the clinical relevance over 1 year, but the decreased risk for health status deterioration may be more pronounced more long term and patients may prefer less treatment burden associated with fingolimod.

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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
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