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格帕茨——漫漫治愈路:一篇叙述性评论。

Gepants - a long way to cure: a narrative review.

机构信息

Headache and Neurosonology Unit, Neurology, Fondazione Policlinico Universitario Campus Bio-Medico Di Roma, 00128, Rome, Italy.

出版信息

Neurol Sci. 2022 Sep;43(9):5697-5708. doi: 10.1007/s10072-022-06184-8. Epub 2022 Jun 2.

Abstract

Calcitonin gene-related peptide (CGRP) is probably the most potent vasodilator in cerebral circulation. Forty years after its discovery, the new CGRP-targeted therapy monoclonal antibodies, and the small molecule gepants, are now available for clinical practice. While randomized controlled trials and real-world experience consistently demonstrated the high efficacy and tolerability of monoclonal antibodies, limited evidence is available to characterize gepants fully. Depending on pharmacokinetics, these CGRP receptor antagonists can be used for acute (ubrogepant, rimegepant, and the not yet approved zavegepant) or preventive (atogepant and rimegepant) migraine treatment. Randomized placebo-controlled trials demonstrated gepants efficacy in treating acute attacks to obtain 2 h pain freedom in about 20% of patients and pain relief in about 60%, while up to 60% of treated patients with episodic migraine may experience a 50% reduction in monthly migraine days. The most common treatment-related emergent adverse events were gastrointestinal (nausea, constipation) for the acute or preventive use. No vascular or hepatic concerns have emerged so far. More studies are ongoing to investigate gepant tolerability and safety also if associated with monoclonal antibodies targeting CGRP and other therapeutic classes. Gepants are also under investigation to treat other painful and non-painful conditions. Real-life studies are necessary to confirm the trials' findings and investigate more practical clinical aspects.

摘要

降钙素基因相关肽(CGRP)可能是脑循环中最有效的血管扩张剂。在发现后的 40 年里,新的 CGRP 靶向治疗单克隆抗体和小分子 gepants 现已可用于临床实践。虽然随机对照试验和真实世界的经验一致表明单克隆抗体具有高疗效和耐受性,但目前可用的证据有限,无法全面描述 gepants。根据药代动力学,这些 CGRP 受体拮抗剂可用于急性(ubrogepant、rimegepant 和尚未批准的 zavegepant)或预防性(atogepant 和 rimegepant)偏头痛治疗。随机安慰剂对照试验表明,gepants 在治疗急性发作方面有效,可使约 20%的患者在 2 小时内疼痛缓解,约 60%的患者疼痛缓解,而接受间歇性偏头痛治疗的患者中多达 60%可能每月偏头痛天数减少 50%。最常见的与治疗相关的急性或预防性使用时出现的不良事件是胃肠道(恶心、便秘)。目前尚未出现血管或肝脏问题。正在进行更多的研究以调查 gepants 的耐受性和安全性,包括与靶向 CGRP 和其他治疗类别的单克隆抗体联合使用。Gepants 也在研究用于治疗其他疼痛和非疼痛疾病。需要真实世界的研究来证实试验结果并调查更实际的临床方面。

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