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特菲达(二甲基富马酸酯)患者的依从性和停药率:来自 Biogen ONE™支持计划的长期加拿大经验。

Adherence and discontinuation rates in patients on Tecfidera™ (dimethyl fumarate): Long-term Canadian experience from the Biogen ONE™ support program.

机构信息

Biogen Canada Inc., 3250 Bloor Street West, East Tower, Suite 1200, Toronto, ON M8X 2X9, Canada.

University of British Columbia, 2211 Wesbrook Mall, Vancouver, BC, Canada.

出版信息

Mult Scler Relat Disord. 2022 Nov;67:104080. doi: 10.1016/j.msard.2022.104080. Epub 2022 Jul 28.

Abstract

BACKGROUND

Tecfidera™ (dimethyl fumarate [DMF]; Biogen) is an oral disease-modifying therapy (DMT) indicated in Canada for the treatment of relapsing-remitting multiple sclerosis (MS). Biogen ONE™, an ongoing Canadian support program, facilitates access to DMF for patients with MS and maintains a database for the purposes of service provision. These data were utilized to assess adherence, persistence, discontinuations, and other outcomes between 2013 and 2021.

METHODS

This non-interventional, retrospective study examined real-world use of DMF prescribed to patients with MS in Canada who were enrolled in the program and received their first dose between April 1, 2013, and June 30, 2021. Follow-up visits and laboratory monitoring occurred based on local standards and per the Canadian product monograph. For adherence and persistence assessments, patients must have had DMF dispensed by specialty pharmacies. Data were collected at patient enrollment, program exit, and throughout the duration of the program. The primary objective was to assess treatment adherence rates to DMF. Secondary objectives included treatment persistence rates, reasons for discontinuation, absolute lymphocyte counts (ALCs), and patient characteristics throughout the duration of the program.

RESULTS

Overall, 12,608 DMF patients from the program were included between April 1, 2013, and June 30, 2021. At enrollment, mean (standard deviation [SD]) age was 40.6 (10.7) years and mean (SD) Expanded Disability Status Scale (EDSS) score was 2.2 (1.4). DMF was initiated as first-line DMT in 48.8% of patients. Of patients assessed (n = 6,848), 90.4% were adherent to DMF (based on medication possession ratio [MPR] ≥ 80%). Adherence (mean MPR) was marginally greater in DMT-naïve than switch patients, and in younger (< 40 years) than older (≥ 40 years) patients (both p < 0.001). Overall persistence on DMF at 24 months was 57.0%. Greater proportions of DMT-naïve patients persisted on DMF versus switch patients at all time points assessed. Persistence rates were comparable between female and male patients for up to 24 months, and between younger (< 40 years) and older (≥ 40 years) patients for up to 36 months. Older patients were more likely to discontinue for reasons related to lymphocytes (≥ 40 years, 16.1% vs. < 40 years, 6.1%) while efficacy reasons were reported with greater frequency in younger patients (≥ 40 years, 10.5% vs. < 40 years, 16.0%). Discontinuations due to gastrointestinal and flushing events occurred most frequently during the first month of treatment and decreased thereafter. Mean ALC decreased during the first year on treatment and subsequently plateaued. Over successive years, changes were observed in characteristics of patients starting on DMF, including decreases in EDSS score, age, and time since diagnosis. The proportion of DMT-naïve patients increased over the years (2013-2014, 26%-27%; 2018-2021, 62%-67%).

CONCLUSIONS

High adherence was found in patients on DMF treatment within the Biogen support program with access to specialty pharmacies. The evolution of the patient population throughout the years suggests a shift towards earlier treatment. These real-world data may support the value of a support program in optimizing the management of patients on DMF treatment. Support programs provide personalized treatment monitoring, which can help minimize early discontinuations and improve adherence to treatment.

摘要

背景

特立氟胺(富马酸二甲酯[DMF];Biogen)是一种在加拿大被批准用于治疗复发缓解型多发性硬化症(MS)的口服疾病修正疗法(DMT)。Biogen ONE 是一个正在进行的加拿大支持项目,旨在为 MS 患者提供 DMF 并维护一个数据库以提供服务。这些数据用于评估 2013 年至 2021 年期间的依从性、持久性、停药和其他结果。

方法

这项非干预性、回顾性研究检查了在加拿大接受 DMF 治疗的 MS 患者的真实世界使用情况,这些患者参加了该项目,并在 2013 年 4 月 1 日至 2021 年 6 月 30 日之间首次接受了 DMF 治疗。根据当地标准和加拿大产品说明书,进行随访就诊和实验室监测。对于依从性和持久性评估,患者必须通过专科药房配药。在患者入组、项目退出和整个项目期间收集数据。主要目的是评估 DMF 的治疗依从率。次要目标包括治疗持久性率、停药原因、绝对淋巴细胞计数(ALC)和整个项目期间的患者特征。

结果

总体而言,在 2013 年 4 月 1 日至 2021 年 6 月 30 日期间,该项目共有 12608 例 DMF 患者。入组时,平均(标准差[SD])年龄为 40.6(10.7)岁,平均(SD)扩展残疾状况量表(EDSS)评分为 2.2(1.4)。48.8%的患者以 DMF 作为一线 DMT 起始治疗。在评估的患者(n=6848)中,90.4%的患者对 DMF 有依从性(基于药物使用比例[MPR]≥80%)。在初治患者中,DMF 的依从性(平均 MPR)略高于换药患者,在年轻(<40 岁)患者中略高于老年(≥40 岁)患者(均 p<0.001)。在 24 个月时,DMF 的总体持久性为 57.0%。在所有评估时间点,初治患者的持久性均高于换药患者。在 24 个月内,男女患者的持久性率相当,在 36 个月内,年轻(<40 岁)和老年(≥40 岁)患者的持久性率相当。老年患者因淋巴细胞相关原因停药的比例更高(≥40 岁,16.1% vs. <40 岁,6.1%),而年轻患者因疗效原因停药的比例更高(≥40 岁,10.5% vs. <40 岁,16.0%)。胃肠道和潮红事件相关的停药最常发生在治疗的第一个月,此后逐渐减少。治疗第一年,平均 ALC 下降,随后趋于稳定。在随后的几年中,开始接受 DMF 治疗的患者特征发生了变化,包括 EDSS 评分、年龄和诊断后时间的变化。初治患者的比例逐年增加(2013-2014 年,26%-27%;2018-2021 年,62%-67%)。

结论

在 Biogen 支持项目中,接受专科药房治疗的 DMF 患者具有较高的依从性。多年来患者人群的演变表明治疗时间提前。这些真实世界的数据可能支持支持项目在优化 DMF 治疗患者管理方面的价值。支持项目提供个性化的治疗监测,有助于最大限度地减少早期停药并提高治疗依从性。

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