Department of Neurology and Centre for Translational Neuro- and Behavioural Sciences (C-TNBS), West German Headache Center, University Hospital Essen, University Duisburg-Essen, Essen, Germany.
Department of Neurology and Centre for Translational Neuro- and Behavioural Sciences (C-TNBS), Division of Clinical Neurooncology, University Hospital Essen, University Duisburg-Essen, Essen, Germany.
Brain Behav. 2022 Jul;12(7):e2662. doi: 10.1002/brb3.2662. Epub 2022 Jun 10.
Current German and European guidelines suggest migraine patients undertake a treatment break after 9 to 12 months of treatment with CGRP (pathway) monoclonal antibodies.
Clinical routine data of highly resistant migraine patients were analyzed before treatment with CGRP monoclonal antibodies (baseline), after 12 months of treatment, and following a treatment break between November 2018 and December 2020 in the West German Headache Centre, University Hospital Essen, Germany. Monthly migraine days (MMD), monthly headache days (MHD), and days of acute medication intake (AMD) were assessed.
Complete clinical data from 46 migraine patients (14 episodic migraine (EM), 32 chronic migraine (CM) patients) treated with erenumab (n = 40), galcanezumab (n = 4), and fremanezumab (n = 2) were analyzed. The mean number of MMDs among EM and CM patients after 12 months of CGRP antibody treatment increased during the treatment break by 5.18 (SE 0.92, p < .001) and 5.06 (SE 1.22, p = .003) days, respectively. There was an increased intake of acute medications among episodic (4.72, SE 0.87, p = .004) and chronic migraine patients (3.01, SE 1.08, p = .013) during treatment break. Eighty-three percent of patients (n = 38) were dissatisfied with the mandatory treatment break. All patients continued with a CGRP (pathway) monoclonal antibody after the mandatory treatment break.
A mandatory break in CGRP (pathway) monoclonal antibody therapy had a negative short-term impact on migraine patients.
目前德国和欧洲的指南建议,接受 CGRP(通路)单克隆抗体治疗 9 至 12 个月后,偏头痛患者应进行治疗中断。
在德国埃森大学医院西德意志头痛中心,分析了在接受 CGRP 单克隆抗体治疗(基线)之前、治疗 12 个月后以及 2018 年 11 月至 2020 年 12 月治疗中断期间高度耐药性偏头痛患者的临床常规数据。评估每月偏头痛天数(MMD)、每月头痛天数(MHD)和急性药物摄入天数(AMD)。
分析了接受依那西普(n=40)、加奈珠单抗(n=4)和弗雷马泽单抗(n=2)治疗的 46 例偏头痛患者(14 例发作性偏头痛(EM),32 例慢性偏头痛(CM)患者)的完整临床数据。在 CGRP 抗体治疗 12 个月后的治疗中断期间,EM 和 CM 患者的 MMD 平均值分别增加了 5.18 天(SE 0.92,p<0.001)和 5.06 天(SE 1.22,p=0.003)。在治疗中断期间,发作性偏头痛患者(4.72,SE 0.87,p=0.004)和慢性偏头痛患者(3.01,SE 1.08,p=0.013)急性药物摄入增加。83%的患者(n=38)对强制性治疗中断不满意。所有患者在强制性治疗中断后继续接受 CGRP(通路)单克隆抗体治疗。
CGRP(通路)单克隆抗体治疗的强制性中断对偏头痛患者有短期负面影响。