Department of Clinical and Molecular Medicine, Sant'Andrea University Hospital, Via di Grottarossa, Rome, Italy.
Regional Referral Headache Centre, Sant'Andrea Hospital, Rome, Italy.
Expert Opin Pharmacother. 2021 May;22(7):907-922. doi: 10.1080/14656566.2020.1862793. Epub 2020 Dec 28.
: Migraine is one of the most common neurological disorders. Nowadays, the 5-HT receptor agonists, namely triptans, are considered as the standard of care for migraine acute treatment. However, triptans have limitations in some patients, such as incomplete pain relief, headache recurrence, and cardiovascular contraindications. New 5-HT receptor agonists, namely ditans, and calcitonin gene-related peptide receptor antagonists, namely gepants, have been developed as migraine-specific treatments.: This paper reviews the available data from RCTs to assess the clinical efficacy, safety, and tolerability profile of lasmiditan, rimegepant, and ubrogepant for the acute treatment of migraine and atogepant for the prevention of migraine.: Available data suggest that lasmiditan, rimegepant, and ubrogepant might not have a clinical efficacy similar to triptans. Lasmiditan did not cause the typical triptan side effects but was associated with central nervous system side effects, causing temporary driving impairment. On the contrary, the new generation of gepants showed a placebo-like tolerability profile and the absence of a specific pattern of side effects. Future studies on lasmiditan and gepants with respect to established effective comparators are mandatory to support phase III results and to help clinicians to balance the benefit/risk profiles of the various acute and preventive medications.
偏头痛是最常见的神经科疾病之一。如今,5-羟色胺(5-HT)受体激动剂,即曲坦类药物,被认为是偏头痛急性治疗的标准治疗方法。然而,曲坦类药物在某些患者中存在局限性,如疼痛缓解不完全、头痛复发和心血管禁忌证。新型 5-HT 受体激动剂,即二氢麦角胺类药物,和降钙素基因相关肽(CGRP)受体拮抗剂,即 gepants,已被开发为偏头痛特异性治疗药物。本文综述了随机对照试验的现有数据,以评估 lasmiditan、rimegepant 和 ubrogepant 治疗偏头痛急性发作和 atogepant 预防偏头痛的临床疗效、安全性和耐受性。现有数据表明,lasmiditan、rimegepant 和 ubrogepant 可能没有与曲坦类药物相似的临床疗效。lasmiditan 不会引起典型的曲坦类副作用,但与中枢神经系统副作用相关,导致短暂的驾驶障碍。相反,新一代的 gepants 显示出类似安慰剂的耐受性,并且没有特定的副作用模式。未来关于 lasmiditan 和 gepants 的研究,需要与已确立的有效对照药物进行比较,以支持 III 期研究结果,并帮助临床医生平衡各种急性和预防性药物的获益/风险比。