Headache Center, Department of Advanced Medical and Surgical Sciences (DAMSS), University of Campania "Luigi Vanvitelli", Piazza Miraglia 2 - I-80138, Naples, Italy.
J Headache Pain. 2022 Jun 13;23(1):69. doi: 10.1186/s10194-022-01436-6.
Clinical trials have demonstrated galcanezumab as safe and effective in migraine prevention. However, real-life data are still lacking and overlook the impact of galcanezumab on those different migraine facets strongly contributing to migraine burden. Herein we report the clinical experience from an Italian real-world setting using galcanezumab in patients with migraine experiencing previous unsuccessful preventive treatments.
Forty-three patients with migraine and failure of at least 3 migraine preventive medication classes received monthly galcanezumab 120 mg s.c. At the first administration and after 3 and 6 months, patients underwent extensive interviews to assess clinical parameters of disease severity. Furthermore, validated questionnaires were administered to explore migraine-related disability, impact, and quality of life as well as symptoms of depression or anxiety, pain catastrophizing, sleep quality and the ictal cutaneous allodynia.
After the third and the sixth administration of monthly galcanezumab 120 mg s.c., headache attacks frequency reduced from 20.56 to 7.44 and 6.37 headache days per month, respectively. Moreover, a significant improvement in headache pain intensity (from 8.95 to 6.84 and 6.21) and duration (from 9.03 to 3.75 and 2.38) as well as in scores assessing migraine related disability and impact, depressive and anxious symptoms, and pain catastrophizing was observed. Furthermore, we demonstrated a significant reduction in the values of "whole pain burden", a composite score derived from the product of the average of headache frequency, intensity, and duration in the last three months.
Real-world data support monthly galcanezumab 120 mg s.c. as a safe and effective preventive treatment in reducing headache frequency, intensity, and duration as well as comorbid depressive or anxious symptoms, pain catastrophizing and quality of life in both episodic and chronic migraine patients with previous unsuccessful preventive treatments. Furthermore, we demonstrated that monthly galcanezumab 120 mg s.c. is able to induce a significant improvement in the scores of "whole pain burden". The latter is a reliable and easy-to-handle tool to be employed in clinical setting to evaluate the effectiveness of preventive drugs (in this case, galcanezumab) or when the decision of continuing the treatment with anti-CGRP mAbs is mandatory.
临床试验已经证明加奈珠单抗在偏头痛预防方面是安全且有效的。然而,实际数据仍然缺乏,并且忽略了加奈珠单抗对那些强烈影响偏头痛负担的不同偏头痛特征的影响。在此,我们报告了一项意大利真实世界研究中的临床经验,该研究使用加奈珠单抗治疗先前预防治疗失败的偏头痛患者。
43 名偏头痛患者和至少 3 种偏头痛预防药物治疗失败的患者每月接受皮下注射 120mg 加奈珠单抗。在第一次给药以及 3 个月和 6 个月后,患者接受了广泛的访谈,以评估疾病严重程度的临床参数。此外,还使用了经过验证的问卷来评估偏头痛相关残疾、影响以及生活质量,以及抑郁或焦虑症状、疼痛灾难化、睡眠质量和发作性皮肤感觉过敏。
每月皮下注射 120mg 加奈珠单抗治疗 3 次和 6 次后,头痛发作频率分别从 20.56 次减少到 7.44 次和 6.37 次/月;头痛天数也分别从 20.56 次减少到 7.44 次和 6.37 次/月。此外,头痛疼痛强度(从 8.95 分降至 6.84 分和 6.21 分)和持续时间(从 9.03 分降至 3.75 分和 2.38 分)以及评估偏头痛相关残疾和影响、抑郁和焦虑症状以及疼痛灾难化的评分也有显著改善。此外,我们还发现“整体疼痛负担”值显著降低,这是一个从过去三个月的头痛频率、强度和持续时间的平均值的乘积衍生而来的综合评分。
真实世界的数据支持每月皮下注射 120mg 加奈珠单抗作为一种安全有效的预防治疗方法,可降低头痛发作频率、强度和持续时间,以及减轻先前预防治疗失败的发作性和慢性偏头痛患者的共患抑郁或焦虑症状、疼痛灾难化和生活质量。此外,我们还证明每月皮下注射 120mg 加奈珠单抗可显著改善“整体疼痛负担”评分。后者是一种可靠且易于处理的工具,可用于临床评估预防药物(在此情况下为加奈珠单抗)的有效性,或者在必须继续使用抗 CGRP mAb 治疗时做出决策。