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在各年龄段的发作性或慢性偏头痛患者中使用依瑞奈玛单抗的安全性和耐受性:安慰剂对照试验的汇总分析。

Safety and tolerability of erenumab in individuals with episodic or chronic migraine across age groups: a pooled analysis of placebo-controlled trials.

机构信息

Department of Neurology, Konventhospital Barmherzige Brüder Linz, Seilerstätte 2, 4020, Linz, Austria.

Novartis Pharmaceuticals, Cambridge, MA, USA.

出版信息

J Headache Pain. 2022 Aug 18;23(1):104. doi: 10.1186/s10194-022-01470-4.

Abstract

BACKGROUND

Erenumab, a fully human monoclonal antibody that targets the calcitonin gene-related peptide receptor, has demonstrated efficacy and safety in the prevention of episodic and chronic migraine. There exists an unmet need to establish the safety of erenumab in older individuals, in view of existing multiple comorbidities, polypharmacy, and age-related physiological changes. This pooled analysis of five large migraine-prevention studies examined the safety of erenumab stratified across age groups, particularly in older populations.

METHODS

Pooled and age-stratified analysis of safety data from the 12-week double-blind treatment phase (DBTP) of five randomized, placebo-controlled Phase 2 and 3 studies of erenumab in participants with episodic or chronic migraine across the age groups < 40 years, 40-49 years, 50-59 years, and ≥ 60 years was completed. The safety of erenumab across age groups was determined by assessing safety endpoints including treatment-emergent adverse events (AEs), serious AEs, and events leading to study drug discontinuation.

RESULTS

Overall, 3345 participants across five studies were randomized to receive either placebo (n = 1359), erenumab 70 mg (n = 1132) or erenumab 140 mg (n = 854); 3176 (94.9%) completed the DBTP, and 169 (5.1%) discontinued, mainly due to participant decision (110; 3.3%). Overall, 1349 (40.6%), 1122 (33.8%), and 850 (25.6%) participants received at least one dose of placebo, erenumab 70 mg, and erenumab 140 mg, respectively. Incidence of treatment-emergent AEs was similar across all age groups for both doses of erenumab (70 mg or 140 mg) and placebo (< 40 years, 44.0% vs 44.4%; 40-49 years, 42.5% vs 49.2%; 50-59 years, 46.5% vs 41.6%; ≥ 60 years, 43.8% vs 59.4%). Incidence of treatment-emergent serious AEs overall, and stratified by age groups for both doses and placebo was low (< 40 years, 0.9% vs 1.2%; 40-49 years, 1.7% vs 1.9%; and 50-59 years, 1.6% vs 1.1%), with no serious AEs reported in participants aged ≥ 60 years. No deaths were reported.

CONCLUSIONS

Erenumab (70 mg or 140 mg) exhibited a similar safety profile compared with placebo across age groups in individuals with episodic or chronic migraine, with no increased emergence of events due to age. Erenumab was well tolerated in older participants with multiple comorbidities, polypharmacy, and age-related physiological changes.

TRIAL REGISTRATION NUMBER

ClinicalTrials.gov Identifiers: NCT02066415, NCT02456740, NCT02483585, NCT03096834, NCT03333109.

摘要

背景

依瑞奈单抗是一种针对降钙素基因相关肽受体的全人源单克隆抗体,在预防发作性和慢性偏头痛方面已被证实具有疗效和安全性。鉴于老年人存在多种合并症、多种药物治疗和与年龄相关的生理变化,因此有必要确定依瑞奈单抗在老年人中的安全性。这五项大型偏头痛预防研究的汇总分析对依瑞奈单抗在不同年龄组中的安全性进行了分层分析,特别是在老年人群中。

方法

对五项依瑞奈单抗治疗发作性或慢性偏头痛的随机、安慰剂对照的 2 期和 3 期研究的 12 周双盲治疗期(DBTP)的安全性数据进行了汇总和年龄分层分析,纳入的参与者年龄分别为<40 岁、40-49 岁、50-59 岁和≥60 岁。通过评估治疗期间出现的不良事件(AE)、严重 AE 和导致研究药物停药的事件等安全性终点来确定依瑞奈单抗在不同年龄组中的安全性。

结果

在五项研究中,共有 3345 名参与者被随机分配接受安慰剂(n=1359)、依瑞奈单抗 70mg(n=1132)或依瑞奈单抗 140mg(n=854);3176 名(94.9%)完成了 DBTP,169 名(5.1%)停药,主要原因是参与者决定(110 名,3.3%)。总体而言,分别有 1349 名(40.6%)、1122 名(33.8%)和 850 名(25.6%)参与者接受了至少一剂安慰剂、依瑞奈单抗 70mg 和依瑞奈单抗 140mg。对于两种剂量的依瑞奈单抗(70mg 或 140mg)和安慰剂,各年龄组治疗期间出现 AE 的发生率相似(<40 岁,44.0% vs 44.4%;40-49 岁,42.5% vs 49.2%;50-59 岁,46.5% vs 41.6%;≥60 岁,43.8% vs 59.4%)。在两个剂量和安慰剂组中,总体上和按年龄组分层的治疗期间出现严重 AE 的发生率均较低(<40 岁,0.9% vs 1.2%;40-49 岁,1.7% vs 1.9%;50-59 岁,1.6% vs 1.1%),≥60 岁的参与者中未报告严重 AE。无死亡报告。

结论

依瑞奈单抗(70mg 或 140mg)在有发作性或慢性偏头痛的个体中与安慰剂相比,在各年龄组中的安全性特征相似,且未因年龄而增加事件的发生。依瑞奈单抗在伴有多种合并症、多种药物治疗和与年龄相关的生理变化的老年患者中具有良好的耐受性。

临床试验注册号

ClinicalTrials.gov 标识符:NCT02066415、NCT02456740、NCT02483585、NCT03096834、NCT03333109。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ecda/9386939/64947ea91d9f/10194_2022_1470_Fig1_HTML.jpg

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