Predictors of Response to Fremanezumab in Migraine Patients with at Least Three Previous Preventive Failures: Post Hoc Analysis of a Prospective, Multicenter, Real-World Greek Registry

被引:8
|
作者
Argyriou, Andreas A. [1 ]
Dermitzakis, Emmanouil V. [2 ]
Xiromerisiou, Georgia [3 ]
Rallis, Dimitrios [4 ]
Soldatos, Panagiotis
Litsardopoulos, Pantelis [1 ]
Vikelis, Michail [5 ]
机构
[1] Agios Andreas State Gen Hosp Patras, Neurol Dept, Headache Outpatient Clin, Patras 26335, Greece
[2] Euromed Gen Clin, Thessaloniki 54645, Greece
[3] Univ Thessaly, Sch Med, Dept Neurol, Larisa 41221, Greece
[4] Tzaneio Gen Hosp Piraeus, Dept Neurol, Athens 18536, Greece
[5] Mediterraneo Hosp, Headache Clin, Glifadha 16673, Greece
关键词
CGRP; monoclonal antibodies; fremanezumab; phenotypes; predictors; response; episodic migraine; chronic migraine; PAIN;
D O I
10.3390/jcm12093218
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Objective: To define, in a real-world population of patients with high-frequency episodic (HFEM) or chronic migraine (CM), the predictive role of socio-demographic or phenotypic profiling of responders to fremanezumab. Patients and methods: Two-hundred and four adult fremanezumab-treated patients with either HFEM or CM, who failed to at least three preventive treatments, provided data at baseline on several individual socio-demographic and phenotypic variables. These variables were analyzed for their ability to independently predict the response (50-74% response rates) or super-response (>= 75% response rates) to fremanezumab. Patients were followed from 3-18 months of fremanezumab exposure. Results: The main finding to emerge from univariate analyses was that three baseline socio-demographic/clinical variables, i.e., age group 41-70 years (p = 0.02); female gender (p = 0.03); patients with HFEM (p = 0.001), and three clinical phenotypic variables, i.e., strict unilateral pain (p = 0.05); pain in the ophthalmic trigeminal branch (p = 0.04); and the "imploding" quality of pain (p = 0.05), were significantly related to fremanezumab response. However, in multivariate analysis, only HFEM (p = 0.02), the presence of strict unilateral (p = 0.03), and pain location in the ophthalmic trigeminal branch (p = 0.036) were independently associated with good fremanezumab response. Allodynia (p = 0.04) was the only clinical predictive variable of super-responsiveness to fremanezumab. Conclusions: A precise phenotypic profiling with identification of pain characteristics consistent with peripheral and/or central sensitization might reliably predict the responsiveness to fremanezumab in migraine prophylaxis.
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页数:10
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