OnabotulinumtoxinA Add-On to Monoclonal Anti-CGRP Antibodies in Treatment-Refractory Chronic Migraine

被引:18
|
作者
Argyriou, Andreas A. A. [1 ]
Dermitzakis, Emmanouil V. V. [2 ]
Xiromerisiou, Georgia [3 ]
Vikelis, Michail [4 ,5 ]
机构
[1] Agios Andreas State Gen Hosp Patras, Neurol Dept, Headache Outpatient Clin, Patras 26352, Greece
[2] Euromed Gen Clin, Thessaloniki 54645, Greece
[3] Univ Hosp Larissa, Fac Med, Sch Hlth Sci, Dept Neurol, Larisa 41110, Greece
[4] Mediterraneo Hosp, Headache Clin, Glifadha 16675, Greece
[5] Glyfada Headache Clin, Glifadha 16675, Greece
关键词
chronic migraine; treatment-refractory migraine; onabotulinumtoxinA; anti-CGRP monoclonal antibodies; dual therapy;
D O I
10.3390/toxins14120847
中图分类号
TS2 [食品工业];
学科分类号
0832 ;
摘要
We sought to assess the effectiveness of combining dual therapy with onabotulinumtoxinA (BTX) add-on to anti-calcitonin gene-related peptide (CGRP) monoclonal antibodies (anti-CGRP MAbs) in treatment-refractory patients with chronic migraine (CM). We retrospectively reviewed the medical files of 19 treatment-refractory patients with CM who had failed to two oral migraine preventatives, at least three consecutive BTX cycles (less than 30% response rate), at least three consecutive sessions with either fremanezumab or erenumab (less than 30% response rate), and were eventually switched to dual therapy with BTX add-on to any of the already-given anti-CGRP MAbs. We then assessed from baseline to each monotherapy or dual intervention predefined efficacy follow-up the changes in the following efficacy outcomes: (i) monthly headache days (MHD), (ii) monthly days with moderate/severe peak headache intensity, and (iii) monthly days with intake of any acute headache medication. Response (50% reduction in MHD) rates, safety, and tolerability were also determined. In the majority of cases (n = 14), dual targeting proved effective and was associated with clinically meaningful improvement in all efficacy variables; 50% response rates (also disability and QOL outcomes) coupled with favorable safety/tolerability. Our results advocate in favor of the view that dual therapy is effective and should be considered in difficult-to-treat CM patients who have failed all available monotherapies.
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页数:11
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