依替珠单抗治疗慢性丛集性头痛的长期安全性、耐受性和疗效(CHRONICLE):开放标签安全性试验

Cristina Tassorelli, Rigmor H Jensen, Peter J Goadsby, Andrew C Charles, Stewart J Tepper, Agneta Henriette Snoer, Mette Krog Josiassen, Christine Borgen Linander, Anders Ettrup, Bjørn Sperling, Neli Boneva
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引用次数: 0

摘要

背景:慢性丛集性头痛是一种罕见但使人非常虚弱的原发性头痛疾病,其特征是每天发作时反复出现剧烈的头痛,缓解期不超过3个月。由于可用的策略很少,治疗具有挑战性。Eptinezumab被批准用于偏头痛预防,是一种人源化单克隆抗体,靶向降钙素基因相关肽,该基因与丛集性头痛的病理生理有关。CHRONICLE试验评估了eptinezumab治疗慢性丛集性头痛的长期安全性和有效性。方法schronicle是一项为期60周、开放标签、固定剂量的试验,在9个国家(丹麦、芬兰、法国、德国、意大利、荷兰、西班牙、英国和美国)的28个头痛专科中心进行。参与者年龄在18-75岁之间,根据《国际头痛疾病分类》第三版诊断为慢性丛集性头痛。Eptinezumab 400mg每12周静脉注射一次。主要目的是通过评估治疗中出现的不良事件来评估eptinezumab的长期安全性和耐受性。通过发作频率、疼痛严重程度和患者报告的结果来评估eptinezumab的疗效。CHRONICLE已在ClinicalTrials.gov (NCT05064397)和EudraCT(2020-001968-28)上注册,并已完成。从2021年9月17日至2023年6月29日,131名参与者入组并接受治疗,其中108名(82%)完成了试验。参与者主要为男性(n=84[64%]),平均年龄为45.2岁(SD 10.8),平均诊断时间为7.3年(5.8)。106名参与者(81%)报告了治疗出现的不良事件,很少导致治疗停药(4名参与者)或输注中断(1名参与者)。三个最常见的治疗不良事件是COVID-19 (n=29;22%),鼻咽炎(n=24;18%)和疲劳(n=23;18%,最常见于输注的第一天)。在试验期间没有发生与治疗相关的严重不良事件,也没有死亡。观察到发作频率、疼痛严重程度和患者报告结果的持续改善。eptinezumab在慢性丛集性头痛患者中具有良好的耐受性,其安全性与先前在偏头痛患者中观察到的相似。虽然观察到超过12个月的临床疗效,但需要随机对照试验(可行时)或具有创新设计的试验来证实这些观察结果的临床相关性。FundingH Lundbeck股份有限公司
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Long-term safety, tolerability, and efficacy of eptinezumab in chronic cluster headache (CHRONICLE): an open-label safety trial

Background

Chronic cluster headache is an uncommon but highly debilitating primary headache disorder characterised by excruciating head pain recurring in daily attacks and without remission periods longer than 3 months. Treatment is challenging due to the few strategies available. Eptinezumab, approved for migraine prevention, is a humanised monoclonal antibody that targets calcitonin gene-related peptide, which has been implicated in the pathophysiology of cluster headaches. The CHRONICLE trial evaluated the long-term safety and efficacy of eptinezumab for the treatment of chronic cluster headache.

Methods

CHRONICLE was a 60-week, open-label, fixed-dose trial conducted in 28 specialist headache centres in nine countries (Denmark, Finland, France, Germany, Italy, Netherlands, Spain, the UK, and the USA). Participants were aged 18–75 years with a diagnosis of chronic cluster headache according to the International Classification of Headache Disorders, 3rd edition. Eptinezumab 400 mg was administered intravenously every 12 weeks. The primary objective was to evaluate the long-term safety and tolerability of eptinezumab by assessing treatment-emergent adverse events. The efficacy of eptinezumab was assessed by attack frequency, pain severity, and patient-reported outcomes. CHRONICLE is registered on ClinicalTrials.gov (NCT05064397) and EudraCT (2020–001968–28) and is completed.

Findings

From Sept 17, 2021, to June 29, 2023, 131 participants were enrolled and treated, of whom 108 (82%) completed the trial. The participants were primarily male (n=84 [64%]), with a mean age of 45·2 years (SD 10·8), and a mean time since diagnosis of 7·3 years (5·8). Treatment-emergent adverse events were reported in 106 participants (81%), with few leading to treatment withdrawal (four participants) or infusion interruption (one participant). The three most common treatment-emergent adverse events were COVID-19 (n=29; 22%), nasopharyngitis (n=24; 18%), and fatigue (n=23; 18%, most commonly on the first day of infusion). There were no treatment-related serious adverse events and no deaths during the trial. Consistent improvements in attack frequency, pain severity, and patient-reported outcomes were observed.

Interpretation

Eptinezumab was generally well tolerated in participants with chronic cluster headache, with a similar safety profile as previously seen in participants with migraine. Although clinical efficacy over 12 months was observed, randomised controlled trials (when feasible) or trials with an innovative design are needed to confirm the clinical relevance of these observations.

Funding

H Lundbeck A/S.
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