Headache and Neurosonology Unit, Neurology, Fondazione Policlinico Campus Bio-Medico, Rome, Italy.
Headache and Pain Unit, IRCCS San Raffaele Pisana, Rome, Italy.
Eur J Neurol. 2023 Jan;30(1):224-234. doi: 10.1111/ene.15563. Epub 2022 Sep 26.
To evaluate the 1-year effectiveness and tolerability of galcanezumab in real life and the prognostic indicators of persistent response.
High-frequency episodic migraine (HFEM) and chronic migraine (CM) patients treated with galcanezumab who completed a 1-year observation were enrolled. The primary outcomes assessed during the 12 months (V1-V12) were the change in monthly migraine days (MMDs) from baseline and the response rates ≥50% in MMDs (MMD ≥50% RR). The secondary outcomes were changes in pain intensity (numerical rating scale [NRS]) and in monthly acute medication intake (MAMI).
We enrolled 191 patients (77.5% CM). Twenty-three patients (12%) dropped out, two for nonserious adverse events. At least 40% of patients took add-on standard preventives from baseline to V12. At V12, MMDs were reduced by 6.0 days in HFEM and by 11.9 days in CM patients (both p < 0.00001); NRS and MAMI were also decreased in both groups (p < 0.00001). One-hundred eight (56.5%) patients presented MMD ≥50% RR for 9 cumulative months (interquartile range=8): we defined this value as the cutoff for a persistent response. Persistent responders were less likely to have a higher body mass index (BMI) (p = 0.007) but more frequently had a good response to triptans (p = 0.005) and MMD ≥50% RR at V1 (p < 0.0000001). Patients without a persistent response were on add-on therapy for longer periods of time (p < 0.001).
Galcanezumab was effective and well-tolerated in the 1-year term, with most patients presenting MMD ≥50% RR for at least 9 months. Triptan response, lower BMI, and MMD ≥50% RR in the first month emerged as predictive factors for a persistent response.
评估加奈珠单抗在真实世界中的 1 年疗效和耐受性,以及持续应答的预测指标。
纳入完成 1 年观察的接受加奈珠单抗治疗的高频发作性偏头痛(HFEM)和慢性偏头痛(CM)患者。在 12 个月(V1-V12)期间评估的主要结局是从基线开始每月偏头痛天数(MMD)的变化和 MMD 减少≥50%的应答率(MMD≥50%RR)。次要结局是疼痛强度(数字评分量表[NRS])和每月急性药物摄入(MAMI)的变化。
我们纳入了 191 名患者(77.5%为 CM)。23 名患者(12%)因非严重不良事件退出,其中 2 名患者因非严重不良事件退出。至少有 40%的患者从基线到 V12 开始使用附加标准预防药物。在 V12 时,HFEM 患者的 MMD 减少了 6.0 天,CM 患者减少了 11.9 天(均 p<0.00001);两组的 NRS 和 MAMI 也均降低(p<0.00001)。108 名(56.5%)患者在 9 个累积月(四分位距=8)时出现 MMD≥50%RR:我们将此值定义为持续应答的截止值。持续应答者的体重指数(BMI)较低(p=0.007),但更频繁地对曲坦类药物有良好反应(p=0.005),且 V1 时 MMD≥50%RR(p<0.0000001)。没有持续应答的患者接受附加治疗的时间更长(p<0.001)。
加奈珠单抗在 1 年的治疗中有效且耐受性良好,大多数患者至少有 9 个月出现 MMD≥50%RR。曲坦类药物反应、较低的 BMI 和第一个月的 MMD≥50%RR 是持续应答的预测因素。