di Cola Francesca Schiano, Bolchini Marco, Caratozzolo Salvatore, Ceccardi Giulia, Cortinovis Matteo, Liberini Paolo, Rao Renata, Padovani Alessandro
Neurology Unit, Department of Clinical and Experimental Sciences, University of Brescia, 25122 Brescia, Italy.
Neurology Unit, Department of Neurological and Vision Sciences, ASST Spedali Civili, 25122 Brescia, Italy.
Neurol Int. 2023 Feb 13;15(1):273-284. doi: 10.3390/neurolint15010017.
The aim of the present study was to assess the migraine outcome, in particular migraine disability, in chronic (CM) and high frequency episodic migraine (HFEM) patients in treatment with galcanezumab.
The present study was conducted at the Headache Centre of Spedali Civili of Brescia. Patients were treated with galcanezumab 120 mg monthly. Clinical and demographical information were collected at the baseline (T0). Data about outcome, analgesics consumption and disability (MIDAS and HIT-6 scores) were collected quarterly.
Fifty-four consecutive patients were enrolled. Thirty-seven patients had a diagnosis of CM, 17 of HFEM. During treatment, patients reported a significant reduction in terms of mean headache/migraine days ( < 0.001), the attacks' pain intensity ( = 0.001) and monthly consumed analgesics ( < 0.001). The MIDAS and HIT-6 scores also documented a significant improvement ( < 0.001). At the baseline, all patients documented a severe degree of disability (MIDAS score ≥ 21). Following six months of treatment, only 29.2% of patients still documented a MIDAS score ≥ 21, with one third of patients documenting little or no disability. A > 50% MIDAS reduction, compared to baseline, was observed in up to 94.6% of patients, following the first three months of treatment. A similar outcome was found for HIT-6 scores. A significant positive correlation was found between headache days and MIDAS at T3 and T6 (T6 > T3), but not baseline.
Monthly prophylactic treatment with galcanezumab was found to be effective in both CM and HFEM, especially in reducing migraine burden and disability.
本研究的目的是评估接受加卡尼单抗治疗的慢性偏头痛(CM)和高频发作性偏头痛(HFEM)患者的偏头痛结局,尤其是偏头痛致残情况。
本研究在布雷西亚市立医院头痛中心进行。患者每月接受120mg加卡尼单抗治疗。在基线期(T0)收集临床和人口统计学信息。每季度收集有关结局、镇痛药使用情况和残疾情况(偏头痛残疾评定量表[MIDAS]和6项头痛影响测试[HIT-6]评分)的数据。
连续纳入54例患者。37例患者诊断为CM,17例为HFEM。在治疗期间,患者报告平均头痛/偏头痛天数显著减少(<0.001)、发作时的疼痛强度显著降低(=0.001)以及每月使用的镇痛药显著减少(<0.001)。MIDAS和HIT-6评分也显示出显著改善(<0.001)。在基线期,所有患者的残疾程度均为重度(MIDAS评分≥21)。经过6个月的治疗,只有29.2%的患者MIDAS评分仍≥21,三分之一的患者残疾程度轻微或无残疾。在治疗的前三个月后,高达94.6%的患者MIDAS评分较基线期降低>50%。HIT-6评分也有类似结果。在T3和T6时(T6>T3),头痛天数与MIDAS之间存在显著正相关,但在基线期不存在。
发现每月使用加卡尼单抗进行预防性治疗对CM和HFEM均有效,尤其是在减轻偏头痛负担和残疾方面。