Long-term reductions in disease impact in patients with chronic migraine following preventive treatment with eptinezumab

被引:8
作者
Blumenfeld, Andrew [1 ]
Ettrup, Anders [2 ]
Hirman, Joe [3 ]
Ebert, Bjarke [2 ]
Cady, Roger [4 ,5 ,6 ]
机构
[1] Los Angeles Headache Ctr, Los Angeles, CA USA
[2] H Lundbeck & Co AS, Copenhagen, Denmark
[3] Pacific Northwest Stat Consulting, Woodinville, WA USA
[4] Lundbeck LLC, Deerfield, IL 60015 USA
[5] RK Consults, Ozark, MO 65721 USA
[6] Missouri State Univ, Springfield, MO 65897 USA
关键词
Eptinezumab; Chronic migraine; Patient-reported outcomes; CGRP monoclonal antibody; INTERNATIONAL BURDEN; PROPHYLACTIC MEDICATIONS; EPISODIC MIGRAINE; DISABILITY; PATTERNS; OUTCOMES;
D O I
10.1186/s12883-022-02774-3
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Background: Eptinezumab is an anti-calcitonin gene-related peptide humanized monoclonal antibody approved for the preventive treatment of migraine in adults. The PREVAIL study demonstrated a favorable safety profile with sustained reductions in overall migraine-related burden in patients with chronic migraine (CM). This post hoc analysis aimed to examine item-level changes in the Migraine Disability Assessment (MIDAS) questionnaire over 2 years in participants with CM on eptinezumab treatment. Methods: PREVAIL was an open-label, phase 3 trial that included 96 weeks of treatment where 128 adults received intravenous eptinezumab administered over 30 min every 12 weeks (wks) for up to 8 doses of 300 mg. MIDAS was administered at baseline, Wk12, and every 12wks thereafter. Two supplementary MIDAS items not included in the total score calculation assessed number of headache days in the past 3 months (MIDAS headache) and average headache pain severity (from 0 [none] to 10 [worst]). MIDAS total scores were summed from 5 items, each quantifying the number of days in the past 3 months with migraine-related disability. Items 1, 3, and 5 assessed absenteeism, namely how many days the patient missed work/school (Q1), household work (Q3), or family/social/leisure activities (Q5). Items 2 and 4 were measures of presenteeism, namely how many days the patient had reduced productivity in work/school (Q2) or household work (Q4). Results: Mean MIDAS headache days decreased from 47.4 (baseline) to 17.1 (Wk12) and 16.3 (Wk104). The average headache pain severity score (0-10) decreased from a mean of 7.3 (baseline) to 5.5 (Wk12) to 4.5 (Wk104). Mean MIDAS scores measuring absenteeism (Q1, 3, 5) changed from 9.7 days at baseline to 3.2 days (Wk12) and to 3.9 days (Wk104). Mean MIDAS scores measuring presenteeism (Q2, 4) at Wk12 decreased from 14.2 days at baseline to 5.2 days (Wk12, 104). Patients categorized with very severe MIDAS disability had a mean total MIDAS score of 84.8, with an average reduction of 56.7 days (Wk12), which was maintained at 32 days at Wk104. Conclusions: Long-term treatment with eptinezumab in patients with CM suggested sustained reductions in MIDAS-quantified disability, consistent with the sustained reductions in headache frequency and pain severity.
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页数:9
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