Anti-CGRP monoclonal antibodies in resistant migraine: preliminary real-world effectiveness and clinical predictors of response at two years

被引:0
|
作者
Pons-Fuster, E. [1 ]
Lozano-Caballero, O. [2 ]
Martin-Balbuena, S. [2 ]
Lucas-Rodenas, C. [2 ]
Mancebo-Gonzalez, A. [1 ]
De Gorostiza-Frias, I. [1 ]
Gonzalez-Ponce, C. M. [1 ]
机构
[1] Virgen Arrixaca Univ Clin Hosp HCUVA, Biomed Res Inst Murcia IMIB, Serv Farm Hosp, Clin Pharm & Therapeut Res Grp, Ctra Madrid Cartagena,S N, Murcia 30120, Spain
[2] Virgen Arrixaca Univ Clin Hosp HCUVA, Headache Unit, Murcia, Spain
关键词
CGRP; Headache; Migraine; Monoclonal antibodies;
D O I
10.1007/s11096-024-01758-2
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
BackgroundMonoclonal antibodies targeting calcitonin gene-related peptide (anti-CGRP mAbs) have shown clinical effectiveness and safety in randomized clinical studies. However, long-term studies in clinical practice remain limited.AimTo assess the long-term effectiveness, clinical predictors and safety of three anti-CGRP mAbs (erenumab, galcanezumab, fremanezumab) in resistant migraine patients.MethodA single-center retrospective study was conducted from December 2019 to June 2023 involving 120 resistant migraine patients who received at least a month of anti-CGRP mAbs treatment. Patients completed a headache diary that included monthly acute medication intake (MAM), monthly migraine days (MMD), adverse events as well as completed Patient-Reported Outcome questionnaires (MIDAS [Migraine Disability Assessment] and Headache Impact Test 6 [HIT-6]). The number of patients achieving a >= 50% reduction in monthly migraine days was determined and classified as >= 50% responders, and baseline parameters and logistic regression between responders and non-responders were analyzed to identify potential predictors of response. Adverse events were registered in every follow-up.ResultsTreatment with anti-CGRP mAbs led to reductions in MIDAS, HIT-6, MMD and MAM from baseline to 6-24 months. At 6-12 months, responders (61% and 57%, respectively) exhibited lower baseline MMD and MAM. Medication overuse was associated with non-responders from 6 to 24 months and it was identified as a negative predictor of treatment effectiveness (OR 0.23, 95% CI 0.07-0.74; p = 0.014).ConclusionAnti-CGRP mAbs prove effectiveness and safety over a 24-month period in a RM population. Patients with no medication overuse and lower basal MMDs and MAM may respond better to anti-CGRP mAbs.
引用
收藏
页码:1317 / 1326
页数:10
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