Basic and Clinical Neurosciences, Institute of Psychiatry, Psychology and Neuroscience, King's College London, London, UK.
NIHR-Wellcome Trust King's Clinical Research Facility/SLaM Biomedical Research Centre, King's College Hospital, London, UK.
Headache. 2019 Jul;59 Suppl 2:3-19. doi: 10.1111/head.13582.
To review and highlight current literature on emerging acute migraine treatments, focusing on CGRP receptor antagonists, gepants, and 5-HT receptor agonists (ditans).
Current acute migraine therapy consists of nonspecific analgesia and triptans. Limitations to these medicines, including lack of efficacy in many patients, side effects and the contraindication of triptans in patients with cardiovascular disease, suggest that there is an unmet need for new treatments. Studies of serotonin pharmacology led to the development of triptans, 5-HT receptor agonists, some of which have actions at the 5-HT receptor. Exploration of the role of calcitonin gene-related peptide (CGRP) has resulted in the development of CGRP receptor antagonists.
The authors performed a literature search of Pubmed and Cochrane databases as well as reviewed abstracts presented at meetings: American Headache Society, American Academy of Neurology, European Headache Federation and the Migraine Trust International Symposium, as well as on-line sources. The authors briefly detail the relevant migraine pathophysiology pertaining to 5-HT receptor and the CGRP pathway relevant to acute therapies. Recent clinical trials of acute therapies in which 5-HT receptor agonists or CGRP receptor antagonists were studied are summarized.
Two 5-HT receptor agonists have reached phase II clinical trials. One, lasmiditan, has completed 2 phase III clinical trials, demonstrating a significant effect for pain freedom and most bothersome symptom at 2 hours. Among the 6 gepants tested for the acute treatment of migraine to date, after issues for some of hepatic safety or efficacy, 2 CGRP receptor antagonists, rimegepant and ubrogepant, have completed phase III trials showing efficacy and safety.
Current available therapies have either been nonspecific or had important limitations, including in patients with cardiovascular risk factors. Phase III clinical trials of lasmiditan, rimegepant and ubrogepant all met their primary endpoints, so the options for migraine-targeted acute therapy will likely soon increase.
回顾和强调当前关于新兴急性偏头痛治疗方法的文献,重点介绍 CGRP 受体拮抗剂、 gepants 和 5-HT 受体激动剂(ditans)。
目前的急性偏头痛治疗方法包括非特异性镇痛剂和曲坦类药物。这些药物存在局限性,包括在许多患者中疗效不佳、副作用以及心血管疾病患者禁用曲坦类药物,这表明存在未满足的新治疗方法需求。对 5-HT 药理学的研究导致了曲坦类药物、5-HT 受体激动剂的开发,其中一些药物在 5-HT 受体上具有作用。对降钙素基因相关肽(CGRP)作用的探索导致了 CGRP 受体拮抗剂的开发。
作者对 Pubmed 和 Cochrane 数据库进行了文献检索,并对在会议上提交的摘要进行了综述,这些会议包括美国头痛协会、美国神经病学会、欧洲头痛联合会和偏头痛信托国际研讨会,以及在线资源。作者简要详细介绍了与 5-HT 受体和急性治疗相关的 CGRP 途径相关的偏头痛病理生理学。总结了最近在急性治疗中研究 5-HT 受体激动剂或 CGRP 受体拮抗剂的临床试验。
有两种 5-HT 受体激动剂已进入 II 期临床试验。其中一种,拉米替坦,已经完成了 2 项 III 期临床试验,证明在 2 小时时对疼痛缓解和最令人困扰的症状有显著效果。迄今为止,已有 6 种 gepants 被测试用于偏头痛的急性治疗,其中一些存在肝安全性或疗效问题,2 种 CGRP 受体拮抗剂,rimegepant 和 ubrogepant,已经完成了 III 期试验,显示出疗效和安全性。
目前可用的治疗方法要么是非特异性的,要么存在重要的局限性,包括在心血管危险因素患者中。拉米替坦、rimegepant 和 ubrogepant 的 III 期临床试验均达到了主要终点,因此偏头痛靶向急性治疗的选择可能很快会增加。