A two years open-label prospective study of OnabotulinumtoxinA 195 U in medication overuse headache: a real-world experience

被引:49
作者
Negro, Andrea [1 ,2 ,6 ]
Curto, Martina [2 ,3 ,4 ]
Lionetto, Luana [5 ]
Martelletti, Paolo [1 ,2 ]
机构
[1] Univ Roma La Sapienza, Dept Clin & Mol Med, Piazzale Aldo Moro 5, I-00185 Rome, Italy
[2] St Andrea Hosp, Reg Referral Headache Ctr, Rome, Italy
[3] Harvard Univ, Sch Med, Dept Psychiat, Boston, MA 02115 USA
[4] McLean Hosp, Bipolar & Psychot Disorders Program, 115 Mill St, Belmont, MA 02178 USA
[5] IDI Ist Dermopat Immacolata IRCSS, Adv Mol Diagnost Unit, Rome, Italy
[6] Univ Roma La Sapienza, St Andrea Hosp, Dept Mol Med, Via Grottarossa 1035-1039, I-00185 Rome, Italy
关键词
Chronic migraine; Medication overuse headache; Migraine abuse; Preventative therapy; OnabotulinumtoxinA; TOXIN TYPE-A; PLACEBO-CONTROLLED PHASE; CHRONIC MIGRAINE; DOUBLE-BLIND; PROPHYLACTIC TREATMENT; PREDICTORS; EFFICACY; BURDEN; CGRP;
D O I
10.1186/s10194-016-0591-3
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Background: The efficacy and safety of OnabotulinumtoxinA (BOTOX (R)) in adults with chronic migraine (CM) were demonstrated in the PREEMPT program. However, the dosage used in this study was flexible from 155 U to 195 U at the physician's discretion. Therefore, the objective of this prospective study was to compare the efficacy and safety of OnabotulinumtoxinA 195 U vs. 155 U for the treatment of CM and medication overuse headache (MOH) during a 2-year period. Methods: We prospectively evaluated the mean reduction in headache days, migraine days, acute pain medication intake days and Headache Impact Test (HIT)-6 score in 172 patients injected with OnabotulinumtoxinA 195 U. Successively, we compared the efficacy measures with data of 155 patients injected with OnabotulinumtoxinA 155 U and followed up for 2 years. All patients were affected by CM and MOH, and failed one or more previous detoxification and preventative therapies. Results: Both OnabotulinumtoxinA 195 U and 155 U reduced significantly the number of headache and migraine days, acute pain medication intake days and HIT-6 score, when compared with the baseline measures. Nevertheless, OnabotulinumtoxinA 195 U proved to be superior of 155 U in all efficacy measures since the first injection and for all the 2 years of treatment, with the exception of the reduction in pain medication intake days that resulted significantly larger with 195 U only after the 4th injection. The safety and tolerability of the two doses were similar and treatment related adverse events were transient and mild-moderate. Conclusions: This study represents the largest and longest post-marketing studies of doses comparison with OnabotulinumtoxinA in a real-life clinical setting. Here, we demonstrate the superior efficacy of OnabotulinumtoxinA 195 U compared to 155 U in CM patients with MOH during a 2-year treatment period with similar safety and tolerability profile.
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页码:1 / 9
页数:9
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