Pain Department and FHU InovPain, CHU Nice - Côte Azur Université, Nice, France
INSERM U1107 Migraine and Trigeminal Pain, Auvergne University, Clermont-Ferrand, France.
J Neurol Neurosurg Psychiatry. 2021 May;92(5):466-472. doi: 10.1136/jnnp-2020-324396. Epub 2021 Jan 5.
To evaluate the effect of erenumab on patient-reported, functional outcomes in patients with episodic migraine (EM) in whom 2-4 preventives were not useful from the Phase 3b LIBERTY study.
As previously reported, 246 patients with EM with 2-4 prior failed preventives were randomised 1:1 to subcutaneous erenumab 140 mg or placebo every 4 weeks for 12 weeks. This analysis evaluated Migraine Physical Function Impact Diary (MPFID), Headache Impact Test (HIT-6) and Work Productivity and Activity Impairment (WPAI) scores at Week 12. P values were nominal without multiplicity adjustment.
Erenumab significantly improved MPFID-Physical Impairment (PI) and Everyday Activities (EA) scores versus placebo (treatment difference (TD) (95% CI) MPFID-PI: -3.5 (-5.7 to -1.2) (p=0.003); MPFID-EA: -3.9 (-6.1 to -1.7)) (p<0.001) at 12 weeks. Patients on erenumab were more likely to have a ≥5-point reduction in MPFID score (OR vs placebo (95% CI) MPFID-EA: 2.1 (1.2 to 3.6); MPFID-PI: 2.5 (1.4 to 4.5)). A similar trend was observed for HIT-6 (TD: -3.0; p<0.001); significantly higher proportions of patients on erenumab reported a ≥5-point reduction (OR (95% CI): 2.4 (1.4 to 4.1)). In three out of four WPAI domains, erenumab showed improvement versus placebo.
At 12 weeks, erenumab was efficacious on functional outcomes in patients with EM in whom 2-4 preventives were not useful.
ClinicalTrials.gov identifier: NCT03096834.
评估依瑞奈umab 对 2-4 种预防药物无效的发作性偏头痛(EM)患者的患者报告的、功能结局的影响,该研究来自于 3b 期 LIBERTY 研究。
正如之前报道的,246 名 2-4 种预防药物失败的 EM 患者以 1:1 的比例随机分配接受皮下注射依瑞奈umab 140mg 或安慰剂,每 4 周 1 次,共 12 周。这项分析评估了偏头痛生理功能影响日记(MPFID)、头痛影响测试(HIT-6)和工作生产力和活动障碍(WPAI)评分在第 12 周的情况。由于没有进行多重性调整,因此 P 值为名义值。
与安慰剂相比,依瑞奈umab 显著改善了 MPFID-生理障碍(PI)和日常活动(EA)评分(治疗差异(TD)(95%置信区间)MPFID-PI:-3.5(-5.7 至-1.2)(p=0.003);MPFID-EA:-3.9(-6.1 至-1.7))(p<0.001)。接受依瑞奈umab 治疗的患者更有可能 MPFID 评分降低≥5 分(与安慰剂相比的比值比(95%置信区间)MPFID-EA:2.1(1.2 至 3.6);MPFID-PI:2.5(1.4 至 4.5))。在 HIT-6 方面也观察到类似的趋势(TD:-3.0;p<0.001);接受依瑞奈umab 治疗的患者报告≥5 分降低的比例显著更高(比值比(95%置信区间):2.4(1.4 至 4.1))。在四个 WPAI 领域中的三个领域,依瑞奈umab 显示出优于安慰剂的改善。
在 12 周时,依瑞奈umab 对 2-4 种预防药物无效的 EM 患者的功能结局有效。
ClinicalTrials.gov 标识符:NCT03096834。