Department of Neurology with Institute of Translational Neurology, University of Münster, Münster, Germany; Department of Neurology, Medical Faculty, Heinrich Heine University Düsseldorf, Düsseldorf, Germany.
Department of Neurology with Institute of Translational Neurology, University of Münster, Münster, Germany.
Mult Scler Relat Disord. 2022 Mar;59:103670. doi: 10.1016/j.msard.2022.103670. Epub 2022 Feb 5.
Alemtuzumab is an anti-CD52 antibody approved for the treatment of relapsing remitting multiple sclerosis (RRMS). The summary of product characteristics (SmPC) provides recommendations on the administration of alemtuzumab to prevent or reduce the risk of serious side effects associated with alemtuzumab infusion, including myocardial ischemia, hemorrhagic stroke, arterial dissection, and pulmonary alveolar hemorrhage. However, real-world implementation of alemtuzumab infusion management recommendations has not been previously assessed.
Here we provide a large-scale multi-center (in- and outpatient) observational study on alemtuzumab infusion management in daily clinical care in Germany (ALEMLL08025; INFUSE-MS; NIS-no. 364). Parameters of infusion management - including infusion administration, clinical and laboratory monitoring - were assessed, compared between study centers and the occurrence of infusion-associated reactions (IARs) was documented. Moreover, the TSQM and MSIS-29 questionnaires were used to quantify patient satisfaction and health-related quality of life.
140 RRMS patients were enrolled in this study. Alemtuzumab infusion regimes (treatment course 1 and 2) were comparable between infusion sites and in accordance with recommendations by the SmPC. Standardization of infusion management was associated with a satisfactory safety profile. IARs were usually mild, headache (13.6%), rash (10.7%), and pyrexia (6.4%) being the most common ones. TSQM and MSIS-29 scores denoted high patient satisfaction and health-related quality of life among RRMS patients treated with alemtuzumab.
In conclusion, our results indicate that infusion management of alemtuzumab is highly standardized and in line with the SmPC. Alemtuzumab treatment and implementation of infusion management recommendations are associated with a satisfactory safety profile regarding the occurrence of IARs, a high patient satisfaction and health-related quality of life as important indicators for the quality of MS care.
阿仑单抗是一种抗 CD52 抗体,已被批准用于治疗复发缓解型多发性硬化症(RRMS)。产品说明书(SmPC)提供了关于阿仑单抗给药的建议,以预防或降低与阿仑单抗输注相关的严重副作用的风险,包括心肌缺血、出血性中风、动脉夹层和肺泡出血。然而,阿仑单抗输注管理建议的实际实施情况尚未得到评估。
本研究提供了一项在德国进行的大规模多中心(门诊和住院)观察性研究,评估阿仑单抗在日常临床护理中的输注管理情况(ALEMLL08025;INFUSE-MS;NIS-no.364)。评估了输注管理参数,包括输注给药、临床和实验室监测,并比较了研究中心之间的差异,并记录了输注相关反应(IARs)的发生情况。此外,还使用 TSQM 和 MSIS-29 问卷来量化患者的满意度和健康相关生活质量。
本研究纳入了 140 例 RRMS 患者。输注部位的阿仑单抗输注方案(治疗疗程 1 和 2)与 SmPC 建议一致。输注管理的标准化与令人满意的安全性概况相关。IARs 通常为轻度,最常见的是头痛(13.6%)、皮疹(10.7%)和发热(6.4%)。TSQM 和 MSIS-29 评分表明,接受阿仑单抗治疗的 RRMS 患者满意度和健康相关生活质量较高。
总之,我们的研究结果表明,阿仑单抗的输注管理高度标准化,符合 SmPC。阿仑单抗治疗和实施输注管理建议与 IARs 的发生、患者满意度和健康相关生活质量等重要指标相一致,表明 MS 护理质量较高。