Department of Neurology, Keio University School of Medicine, Japan.
Department of Neurology, Keio University School of Medicine, Japan; Division of Drug Informatics, Keio University Faculty of Pharmacy, Japan.
J Neurol Sci. 2023 Oct 15;453:120811. doi: 10.1016/j.jns.2023.120811. Epub 2023 Sep 16.
Anti-calcitonin gene-related peptide monoclonal antibodies (CGRPmAbs) have dramatically changed preventive treatment options for patients with migraine. Although there is emerging real-world evidence on the use of CGRPmAbs globally, the change in efficacy and safety after switching between CGRPmAbs owing to patients' frequency of hospital visits preference remains unknown.
We conducted a single-centre, retrospective, real-world study of patients with migraine who first received galcanezumab for 3 or 4 months and then switched to fremanezumab at Keio University Hospital. We investigated changes in monthly migraine days (MMD), responder rate, and adverse effects such as injection site reactions.
MMD increased only by 0.7 (95% CI, -4.1-5.5; p = 0.748) after 4 months of treatment with fremanezumab (6.1, 95% CI, 2.3-9.9) compared to before switching (5.4, 95% CI, 2.2-8.6). Furthermore, switching from galcanezumab to fremanezumab produced only minor adverse events, such as injection site reactions.
After switching from galcanezumab to fremanezumab out of the desire to visit the hospital less often, the reduction in MMD compared to baseline was sustained, and no serious adverse effects were observed.
抗降钙素基因相关肽单克隆抗体(CGRPmAb)显著改变了偏头痛患者的预防治疗选择。尽管全球范围内有关于 CGRPmAb 使用的新兴真实世界证据,但由于患者就诊频率的偏好,在 CGRPmAb 之间切换后的疗效和安全性变化尚不清楚。
我们在庆应义塾大学医院进行了一项单中心、回顾性、真实世界的研究,纳入了首次接受加奈珠单抗治疗 3 或 4 个月后转换为依瑞奈珠单抗的偏头痛患者。我们调查了每月偏头痛天数(MMD)、应答率和不良反应(如注射部位反应)的变化。
与转换前(5.4,95%CI,2.2-8.6)相比,转换为依瑞奈珠单抗治疗 4 个月后 MMD 仅增加 0.7(95%CI,-4.1-5.5;p=0.748)(6.1,95%CI,2.3-9.9)。此外,从加奈珠单抗转换为依瑞奈珠单抗仅产生轻微的不良反应,如注射部位反应。
出于减少就诊频率的愿望,从加奈珠单抗转换为依瑞奈珠单抗后,与基线相比,MMD 的减少得以维持,且未观察到严重不良反应。