TAURUS-MS II: real-world use of teriflunomide in Germany and changes in treatment patterns over time.

IF 4.7 2区 医学 Q1 CLINICAL NEUROLOGY Therapeutic Advances in Neurological Disorders Pub Date : 2024-05-27 eCollection Date: 2024-01-01 DOI:10.1177/17562864241252722
Boris-Alexander Kallmann, Georg Zu Eulenburg, Jennifer S Kullmann, Mathias Mäurer
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Abstract

Background: Teriflunomide is a once-daily oral disease-modifying therapy (DMT) for the treatment of relapsing-remitting multiple sclerosis (RRMS). Only limited information is available about its real-world use and changes over time.

Objectives: To collect real-world data on teriflunomide use in clinical routine (and comparison to the previously conducted study TAURUS-MS).

Design: National, open, non-interventional, prospective, multicenter study.

Methods: TAURUS-MS II was conducted at 220 German sites between July 2017 and March 2022, including RRMS patients treated with teriflunomide. Data on patient demographics, MS history, previous treatment, therapy satisfaction, and safety were collected.

Results: In total, 752 patients were included (65% female) with a mean age (±standard deviation) of 43 ± 11 years. Sixty-six percent had DMT before, and 46% had discontinued their last pretreatment ≤6 months prior to study entry. Among the latter, previous DMTs were interferon (21%), glatiramer acetate (11%), and dimethyl fumarate (9%), and reasons for discontinuation were adverse events (AEs; 55%) and insufficient efficacy (16%). Over 24 months, the mean treatment Satisfaction Questionnaire for Medication scores improved by 6 ± 29 points on effectiveness, 8 ± 20 on convenience, and 12 ± 25 on global satisfaction. The mean number of MS relapses decreased from 0.81 ± 0.81 in the 24 months prior to 0.27 ± 0.57 within 24 months after study entry. Non-serious AEs occurred in 423 patients (56%) and serious AEs in 49 patients (7%). Most reported AEs were alanine aminotransferase increase (11%), hypertension (8%), and alopecia (7%). Compared to TAURUS-MS, patients in TAURUS-MS II were younger, had a higher employment rate, and a higher share of treatment-naïve patients.

Conclusion: Mean number of relapses was significantly reduced. Patient satisfaction was significantly improved compared to previous DMT. Tolerability was comparable to previous trials.

Trial registration: Bundesinstitut für Arzneimittel und Medizinprodukte public database for non-interventional studies, number 7138.

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TAURUS-MS II:德国特立氟胺的实际使用情况和治疗模式的长期变化。
背景介绍特立氟胺是一种治疗复发缓解型多发性硬化症(RRMS)的每日一次口服疾病缓解疗法(DMT)。有关其实际使用情况和随时间推移发生变化的信息非常有限:收集特立氟胺在临床常规治疗中的实际使用数据(并与之前进行的TAURUS-MS研究进行比较):设计:全国性、开放、非干预、前瞻性、多中心研究:TAURUS-MS II于2017年7月至2022年3月期间在德国220个医疗点进行,包括接受特立氟胺治疗的RRMS患者。研究收集了患者人口统计学、多发性硬化症病史、既往治疗、治疗满意度和安全性等数据:共纳入752名患者(65%为女性),平均年龄(±标准差)为43±11岁。66%的患者曾接受过DMT治疗,46%的患者在研究开始前6个月内停止了最后一次治疗。在后者中,以前使用过的 DMT 为干扰素(21%)、醋酸格拉替雷(11%)和富马酸二甲酯(9%),停药原因为不良事件(AE;55%)和疗效不佳(16%)。在24个月内,治疗药物满意度问卷的平均得分在有效性方面提高了6±29分,在方便性方面提高了8±20分,在总体满意度方面提高了12±25分。多发性硬化症复发的平均次数从研究开始前24个月的0.81±0.81次减少到研究开始后24个月的0.27±0.57次。423名患者(56%)发生了非严重AE,49名患者(7%)发生了严重AE。报告最多的不良反应是丙氨酸氨基转移酶升高(11%)、高血压(8%)和脱发(7%)。与TAURUS-MS相比,TAURUS-MS II的患者更年轻,就业率更高,且有更多的患者对治疗一无所知:结论:平均复发次数明显减少。结论:复发的平均次数明显减少,患者的满意度与之前的 DMT 相比明显提高。耐受性与之前的试验相当:试验注册:联邦药品和医疗用品研究所非干预性研究公共数据库,编号7138。
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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来源期刊
CiteScore
8.30
自引率
1.70%
发文量
62
审稿时长
15 weeks
期刊介绍: Therapeutic Advances in Neurological Disorders is a peer-reviewed, open access journal delivering the highest quality articles, reviews, and scholarly comment on pioneering efforts and innovative studies across all areas of neurology. The journal has a strong clinical and pharmacological focus and is aimed at clinicians and researchers in neurology, providing a forum in print and online for publishing the highest quality articles in this area.
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