Barbanti Piero, Orlando Bianca, Egeo Gabriella, d'Onofrio Florindo, Doretti Alberto, Messina Stefano, Autunno Massimo, Messina Roberta, Filippi Massimo, Fiorentini Giulia, Rotondi Cristina, Bonassi Stefano, Aurilia Cinzia
Headache and Pain Unit, IRCCS San Raffaele, Via della Pisana 235, 00163 Rome, Italy.
San Raffaele University, 00166 Rome, Italy.
Brain Sci. 2024 Jun 30;14(7):672. doi: 10.3390/brainsci14070672.
We conducted a multicenter, prospective study (EMBRACE) evaluating the real-life effectiveness, safety, and tolerability of eptinezumab (100 mg/300 mg)-a monoclonal antibody targeting the calcitonin-gene-related peptide (anti-CGRP mAb)-in high-frequency episodic migraine (HFEM) or chronic migraine (CM). The primary endpoint was the change in monthly migraine days (MMD) for HFEM or monthly headache days (MHD) for CM at weeks 9-12 compared to baseline. The secondary endpoints included changes in monthly analgesic intake (MAI), Numerical Rating Scale (NRS), Headache Impact Test (HIT-6), Migraine Disability Assessment Scale (MIDAS), Migraine Interictal Burden Scale (MIBS-4), and responder rates. The safety analysis involved 44 subjects; the effectiveness analysis included 26 individuals. Eptinezumab was well-tolerated. In CM patients, eptinezumab significantly reduced MHD (-16.1 ± 9.9, < 0.001), MAI, NRS, HIT-6, MIDAS, and MIBS-4. In HFEM patients, it significantly reduced NRS, HIT-6, MIDAS, and MIBS-4, though reductions in MMD (-3.3 ± 4.5) and MAI were not statistically significant. Overall, ≥50% and ≥75% response rates were 61.5% and 30.8%, respectively (60% and 30% in non-responders to subcutaneous anti-CGRP mAbs). The clinical change was rated as much or very much improved by 61.0% of the patients. Eptinezumab demonstrated high effectiveness, safety, and tolerability in real-life among hard-to-treat migraine patients with multiple treatment failures, including anti-CGRP mAbs.
我们开展了一项多中心前瞻性研究(EMBRACE),评估依普他命单抗(100毫克/300毫克)——一种靶向降钙素基因相关肽的单克隆抗体(抗CGRP单克隆抗体)——在高频发作性偏头痛(HFEM)或慢性偏头痛(CM)患者中的实际疗效、安全性和耐受性。主要终点是与基线相比,第9至12周时HFEM患者的每月偏头痛天数(MMD)变化或CM患者的每月头痛天数(MHD)变化。次要终点包括每月镇痛药摄入量(MAI)、数字评定量表(NRS)、头痛影响测试(HIT-6)、偏头痛残疾评估量表(MIDAS)、偏头痛发作间期负担量表(MIBS-4)的变化以及缓解率。安全性分析纳入了44名受试者;疗效分析包括26名个体。依普他命单抗耐受性良好。在CM患者中,依普他命单抗显著降低了MHD(-16.1±9.9,<0.001)、MAI、NRS、HIT-6、MIDAS和MIBS-4。在HFEM患者中,它显著降低了NRS、HIT-6、MIDAS和MIBS-4,尽管MMD(-3.3±4.5)和MAI的降低无统计学意义。总体而言,≥50%和≥75%的缓解率分别为61.5%和30.8%(皮下注射抗CGRP单克隆抗体无反应者中分别为60%和30%)。61.0%的患者将临床变化评为改善很多或非常多。在现实生活中,对于包括抗CGRP单克隆抗体治疗失败在内的多种治疗失败的难治性偏头痛患者,依普他命单抗显示出高效、安全和耐受性良好。