Department of Neurology, Mayo Clinic, Phoenix, AZ, USA.
Eli Lilly and Company, Indianapolis, IN, USA.
J Headache Pain. 2021 Mar 25;22(1):15. doi: 10.1186/s10194-021-01230-w.
Galcanezumab is a monoclonal antibody (mAb) that binds calcitonin gene-related peptide (CGRP) and is indicated for the preventive treatment of migraine. Galcanezumab demonstrated early onset of effect in patients with migraine but it is unknown whether the same holds true for patients who have not benefited from multiple prior migraine preventives.
Patients with episodic or chronic migraine from a 3-month, randomized, double-blind, placebo-controlled, phase 3b study (CONQUER) who had 2 to 4 migraine preventive medication category failures in the past 10 years were randomized 1:1 to placebo (N = 230) or galcanezumab 120 mg/month (240 mg loading dose; N = 232). In this post-hoc analysis, change from baseline in number of monthly and weekly migraine headache days was assessed. Monthly onset of effect was the earliest month at which significant improvement with galcanezumab compared to placebo was achieved and maintained at all subsequent months. Weekly onset was the initial week at which statistical separation was achieved and maintained at all subsequent weeks during that month. Proportion of patients with migraine headache days in the first week of treatment, and patients achieving ≥50%, ≥75%, and 100% response by month and week were also assessed.
Galcanezumab-treated patients had a significantly greater reduction in monthly migraine headache days starting at month 1, which remained significant for all subsequent months compared to placebo (all p ≤ 0.0001, month 1 mean change from baseline: placebo - 0.7; galcanezumab - 4.0). Weekly migraine headache days was significantly reduced in galcanezumab-treated patients starting at week 1 and continued for each subsequent week of month 1 compared to placebo (all p < 0.01, week 1 mean change from baseline: placebo - 0.2; galcanezumab - 1.1). A significantly smaller percentage of patients had a migraine headache on the first day after galcanezumab treatment compared to placebo (28.4% vs 39.2%) and at each subsequent day during week 1 (all p < 0.05). A greater proportion of galcanezumab-treated patients achieved ≥50%, ≥75%, and 100% response at months 1-3 (all p < 0.05) and at weeks 1-4 of month 1 compared to placebo (all p < 0.01).
Galcanezumab showed early onset of effect beginning the day after treatment initiation in patients who had not previously benefited from migraine preventive treatments.
ClinicalTrials.gov , NCT03559257 . Registered 18 June 2018.
加奈珠单抗是一种与降钙素基因相关肽(CGRP)结合的单克隆抗体(mAb),用于偏头痛的预防性治疗。加奈珠单抗在偏头痛患者中表现出早期起效,但对于那些未从多种既往偏头痛预防药物中获益的患者,其是否同样有效尚不清楚。
CONQUER 是一项为期 3 个月、随机、双盲、安慰剂对照的 3b 期研究,纳入了来自该研究的发作性或慢性偏头痛患者,这些患者在过去 10 年中有 2 至 4 次偏头痛预防药物治疗失败。他们被随机 1:1 分配至安慰剂(n=230)或加奈珠单抗 120mg/月(240mg 负荷剂量;n=232)。在这项事后分析中,评估了从基线到每月和每周偏头痛头痛天数的变化。每月起效是指与安慰剂相比,加奈珠单抗最早达到并在所有后续月份保持显著改善的月份。每周起效是指在当月的最初一周达到并在所有后续周保持统计学分离的初始周。还评估了治疗的第一周偏头痛头痛天数的患者比例,以及达到每月和每周≥50%、≥75%和 100%反应的患者比例。
加奈珠单抗治疗的患者每月偏头痛头痛天数的减少从第 1 个月开始显著,与安慰剂相比,所有后续月份均保持显著(均 p≤0.0001,第 1 个月的平均基线变化:安慰剂-0.7;加奈珠单抗-4.0)。每周偏头痛头痛天数在第 1 周开始显著减少,并在第 1 个月的每个后续周持续减少,与安慰剂相比(均 p<0.01,第 1 周的平均基线变化:安慰剂-0.2;加奈珠单抗-1.1)。与安慰剂相比,在加奈珠单抗治疗的患者中,在治疗后的第一天(28.4% vs 39.2%)和第 1 周的后续每一天(均 p<0.05),偏头痛头痛的患者比例显著较小。与安慰剂相比,在第 1-3 个月(均 p<0.05)和第 1 个月的第 1-4 周(均 p<0.01),更多的加奈珠单抗治疗的患者达到≥50%、≥75%和 100%的反应。
在那些以前未从偏头痛预防治疗中获益的患者中,加奈珠单抗在治疗后第一天就显示出早期起效。
ClinicalTrials.gov,NCT03559257。2018 年 6 月 18 日注册。