Professor of Neurology, Geisel School of Medicine at Dartmouth, Hanover, NH.
Director, Dartmouth Headache Center, Neurology Department, Dartmouth Hitchcock Medical Center, Lebanon, NH.
Headache. 2018 Nov;58 Suppl 3:238-275. doi: 10.1111/head.13379. Epub 2018 Sep 22.
Objective - To briefly describe the history of and available data on anti-calcitonin gene-related peptide (CGRP) therapies for headache. Background - CGRP was proposed as a target for primary headache therapies. Translational research involved moving from delineating the relationships between CGRP and primary headaches and the clinical development of anti-CGRP treatments. The first anti-CGRP treatment, an intravenous CGRP-receptor antagonist or gepant, olcegepant, was described as effective in terminating migraines in humans in 2004. Methods - The author briefly reviews some of the pathophysiology and translational research that led to the development of the gepants initially and then subsequently to the anti-CGRP and anti-CGRP receptor monoclonal antibodies. All accessible randomized controlled trials, abstracts, platform presentations, and press releases on the monoclonal antibody trials are summarized. The trajectory from bench research to the approval of the first anti-CGRP receptor monoclonal antibody for clinical use in migraine prevention, erenumab, is discussed, as well as potential clinical uses of the anti-CGRP treatments. Results - The US Food and Drug Administration (FDA) approved erenumab, an anti-CGRP receptor monoclonal antibody, for prevention of migraine May 17, 2018. At the time of this writing (May 2018), 2 other anti-CGRP monoclonal antibodies have been submitted to the FDA for the indication of prevention of migraine, galcanezumab and fremanezumab. Galcanezumab has reportedly shown effectiveness in preventing episodic cluster headache as well, although has not yet been submitted to the FDA for this indication. Eptinezumab will likely be submitted to the FDA for prevention of migraine later in 2018. Two gepants, ubrogepant and rimegepant, have completed positive pivotal trials for acute treatment of migraine, but have not yet been submitted to the FDA for this indication. Conclusions - The development of anti-CGRP therapies opens a new era in the acute and preventive treatment of primary headache disorders.
目的-简要描述抗降钙素基因相关肽(CGRP)治疗头痛的历史和现有数据。背景-CGRP 被提议作为原发性头痛治疗的靶点。转化研究包括从描绘 CGRP 与原发性头痛之间的关系以及抗 CGRP 治疗的临床发展。第一种抗 CGRP 治疗方法,即静脉内 CGRP 受体拮抗剂或 gepant,奥昔替泮,于 2004 年被描述为有效终止人类偏头痛。方法-作者简要回顾了一些导致 gepants 最初开发,然后是抗 CGRP 和抗 CGRP 受体单克隆抗体开发的病理生理学和转化研究。总结了所有可获得的关于单克隆抗体试验的随机对照试验、摘要、平台演讲和新闻稿。讨论了从基础研究到第一个用于预防偏头痛的抗 CGRP 受体单克隆抗体(erenumab)获得批准的轨迹,以及抗 CGRP 治疗的潜在临床用途。结果-美国食品和药物管理局(FDA)于 2018 年 5 月 17 日批准了用于预防偏头痛的 erenumab,一种抗 CGRP 受体单克隆抗体。在撰写本文时(2018 年 5 月),另外 2 种抗 CGRP 单克隆抗体已提交给 FDA 用于预防偏头痛,即 galcanezumab 和 fremanezumab。据报道,galcanezumab 也有效预防发作性丛集性头痛,尽管尚未提交给 FDA 用于此适应症。Eptinezumab 可能会在 2018 年晚些时候提交给 FDA 用于预防偏头痛。两种 gepants,ubrogepant 和rimegepant,已完成用于急性偏头痛治疗的阳性关键试验,但尚未提交给 FDA 用于此适应症。结论-抗 CGRP 治疗的发展开辟了原发性头痛疾病急性和预防性治疗的新纪元。