Suppr超能文献

氯法拉滨片与芬戈莫德治疗活跃期多发性硬化症的疗效比较:一项真实世界研究。

Comparative effectiveness of cladribine tablets versus fingolimod in the treatment of highly active multiple sclerosis: A real-world study.

机构信息

Queen Square MS Centre, University College London Institute of Neurology and National Institute for Health and Care Research (NIHR) University College London Hospitals Biomedical Research Centre, London, UK.

Ruhr-University Bochum & St. Josef-Hospital, Bochum, Germany.

出版信息

Mult Scler Relat Disord. 2023 Aug;76:104791. doi: 10.1016/j.msard.2023.104791. Epub 2023 Jun 3.

Abstract

BACKGROUND

Cladribine tablets and fingolimod have similar marketing authorisations in Europe for the treatment of patients with highly active relapsing multiple sclerosis (HA-RMS). In the absence of direct head-to-head studies, real-world data are important to assess the comparative effectiveness of these oral disease-modifying therapies (DMTs). The primary objective of the present study was to compare relapse rates between patients who received either cladribine tablets or fingolimod.

METHODS

This multicentre retrospective study conducted in the United Kingdom and Germany assessed non-inferiority in relapse rates of cladribine tablets versus fingolimod in HA-RMS patients over a 12-month period. Eligible patients who initiated treatment with cladribine tablets or fingolimod at least 12 months prior to the screening date were sampled consecutively until the target sample size was reached. Patients were censored at discontinuation of study treatment, commencement of another DMT, death, loss to follow-up, or at 12 months post-baseline, whichever happened earliest. The primary analytic timeframe for physician-confirmed relapse outcomes was the study effectiveness period (nine months of follow-up after an initial 12 weeks of treatment). Propensity score analysis was applied based on the inverse probability of treatment weighting approach.

RESULTS

The primary analytic cohort consisted of 1,095 HA-RMS patients: 610 (55.7%) receiving cladribine tablets and 485 (44.3%) receiving fingolimod. Fewer patients discontinued cladribine tablets and/or switched to another DMT compared with fingolimod (0.2% versus 3.5%, respectively). The primary endpoint, adjusted annualised relapse rate (ARR), was 0.10 (95% confidence interval [CI]: 0.07-0.14) for cladribine tablets and 0.14 (95% CI: 0.10-0.20) for fingolimod. The adjusted ARR ratio of cladribine tablets versus fingolimod was 0.68 (95% CI: 0.42-1.11). Given the entire 95% CI was less than the non-inferiority margin of 1.2, cladribine tablets was non-inferior to fingolimod.

CONCLUSIONS

In this real-world retrospective cohort study, cladribine tablets demonstrated comparable effectiveness to fingolimod at one year following treatment initiation. The full treatment dosage of cladribine tablets is completed over two years and so these results may be conservative.

摘要

背景

在欧洲,克拉屈滨片和芬戈莫德都有类似的上市许可,用于治疗活动期多发性硬化症(RRMS)患者。由于缺乏头对头研究,真实世界数据对于评估这些口服疾病修正治疗药物(DMT)的疗效具有重要意义。本研究的主要目的是比较接受克拉屈滨片或芬戈莫德治疗的患者之间的复发率。

方法

本研究为在英国和德国开展的多中心回顾性研究,评估了在 12 个月的时间内,克拉屈滨片治疗 RRMS 患者的疗效是否不劣于芬戈莫德。连续入选至少在筛选日期前 12 个月开始接受克拉屈滨片或芬戈莫德治疗的合格患者,直至达到目标样本量。患者在研究药物停药、开始另一种 DMT、死亡、失访或基线后 12 个月时进行删失,以最早发生者为准。医师确认的复发结局的主要分析时间范围为研究有效性期间(治疗最初的 12 周后 9 个月的随访)。采用基于治疗反概率加权的倾向评分分析。

结果

主要分析队列包括 1095 例 RRMS 患者:610 例(55.7%)接受克拉屈滨片治疗,485 例(44.3%)接受芬戈莫德治疗。与芬戈莫德相比,克拉屈滨片组停药和/或转换为另一种 DMT 的患者更少(分别为 0.2%和 3.5%)。克拉屈滨片的主要终点(调整后的年化复发率,ARR)为 0.10(95%置信区间[CI]:0.07-0.14),芬戈莫德为 0.14(95%CI:0.10-0.20)。克拉屈滨片与芬戈莫德的调整后 ARR 比值为 0.68(95%CI:0.42-1.11)。由于整个 95%CI 小于 1.2 的非劣效性边界,因此克拉屈滨片不劣于芬戈莫德。

结论

在这项真实世界的回顾性队列研究中,克拉屈滨片在治疗开始后 1 年时的疗效与芬戈莫德相当。克拉屈滨片的完整治疗剂量在两年内完成,因此这些结果可能较为保守。

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验