Reduction in acute migraine-specific and non-specific medication use in patients treated with erenumab: post-hoc analyses of episodic and chronic migraine clinical trials

被引:10
|
作者
Tepper, Stewart J. [1 ]
Ashina, Messoud [2 ]
Reuter, Uwe [3 ]
Hallstroem, Yngve [4 ]
Broessner, Gregor [5 ]
Bonner, Jo H. [6 ]
Picard, Hernan [7 ]
Cheng, Sunfa [7 ]
Chou, Denise E. [7 ]
Zhang, Feng [7 ]
Klatt, Jan [8 ]
Mikol, Daniel D. [7 ]
机构
[1] Geisel Sch Med Dartmouth, Hanover, NH 03755 USA
[2] Univ Copenhagen, Rigshosp Glostrup, Fac Hlth & Med Sci, Dept Neurol,Danish Headache Ctr, Copenhagen, Denmark
[3] Charite Univ Med Berlin, Dept Neurol, Berlin, Germany
[4] St Gorans Univ Hosp, Neuro Ctr, Stockholm, Sweden
[5] Med Univ Innsbruck, Dept Neurol, Headache Outpatient Clin, Innsbruck, Austria
[6] Mercy Clin Neurol & Headache Ctr, St Louis, MO USA
[7] Amgen Inc, Thousand Oaks, CA 91320 USA
[8] Novartis Pharma AG, CH-4002 Basel, Switzerland
来源
JOURNAL OF HEADACHE AND PAIN | 2021年 / 22卷 / 01期
关键词
CGRP receptor; Chronic migraine; Episodic migraine; Erenumab; Migraine-specific; DOUBLE-BLIND; PREVENTIVE TREATMENT; UNITED-STATES; AMG; 334; PLACEBO; ONABOTULINUMTOXINA; EFFICACY; OVERUSE; SAFETY; COSTS;
D O I
10.1186/s10194-021-01292-w
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Background In patients with migraine, overuse of acute medication, including migraine-specific medication (MSM) such as triptans and ergots, can lead to adverse health outcomes, including development of medication overuse headache. Here, we examined the effect of erenumab on reducing acute medication use, in particular MSM, in patients with episodic migraine (EM) and chronic migraine (CM). Methods The current post-hoc analyses were based on data from the double-blind treatment phase (DBTP) of two erenumab studies, a pivotal EM (N = 955) and a pivotal CM (N = 667) trial, and their respective extensions. Patients were administered subcutaneous placebo or erenumab (70 or 140 mg) once monthly. Daily acute headache medication use (including MSM and non-MSM) was recorded using an electronic diary during a 4-week pretreatment baseline period until the end of the treatment period. Outcome measures included change in monthly acute headache medication days (HMD) in acute headache medication users at baseline, and changes in monthly MSM days (MSMD) in MSM users at baseline and non-MSMD in non-MSM users at baseline. Results In total, 60 and 78 % of patients (all acute headache medication users) with EM and CM used MSM at baseline, respectively. For acute headache medication users, the change in mean monthly acute HMD over Months 4, 5 and 6 compared with the pre-DBTP was 1.5, 2.5, and 3.0 for placebo, erenumab 70 mg and 140 mg, respectively for the EM study. The respective change in monthly MSMD in MSM users was 0.5, 2.1 and 2.8, and in monthly non-MSMD in non-MSM users was 2.3, 2.6, and 2.7. In the acute headache medication users at baseline, the change in monthly acute HMD at Month 3 compared with pre-DBTP was 3.4, 5.5, and 6.5 for placebo, erenumab 70 mg and 140 mg, respectively for the CM study. The respective change in monthly MSMD in MSM users was 2.1, 4.5, and 5.4, and in monthly non-MSMD in non-MSM users was 5.9, 6.4, and 6.6. Reductions in MSMD versus placebo were sustained in the extension periods of both studies. Erenumab was also associated with a higher proportion of MSM users achieving >= 50 %, >= 75 and 100 % reduction from baseline in monthly MSMD versus placebo in both EM and CM. Conclusions In both EM and CM, treatment with erenumab is associated with a significant and sustained reduction in the use of acute headache medication, in particular MSM.
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页数:14
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