IncobotulinumtoxinA Efficacy/Safety in Upper-Limb Spasticity in Pediatric Cerebral Palsy: Randomized Controlled Trial

被引:10
作者
Dabrowski, Edward [1 ]
Chambers, Henry G. [2 ]
Gaebler-Spira, Deborah [3 ]
Banach, Marta [4 ]
Kanovsky, Petr [5 ,6 ]
Dersch, Hanna [7 ]
Althaus, Michael [7 ]
Geister, Thorin L. [7 ]
Heinen, Florian [8 ,9 ]
机构
[1] Beaumont Pediat Phys Med & Rehabil Royal Oak, Royal Oak, MI 48073 USA
[2] Rady Childrens Hosp, San Diego, CA USA
[3] Northwestern Feinberg Sch, Shirley Ryan AbilityLab, Chicago, IL USA
[4] Jagiellonian Univ, Coll Med, Dept Neurol, Krakow, Poland
[5] Palacky Univ Olomouc, Fac Med & Dent, Olomouc, Czech Republic
[6] Palacky Univ Olomouc, Univ Hosp, Olomouc, Czech Republic
[7] Merz Pharmaceut GmbH, Frankfurt, Germany
[8] Ludwig Maximilians Univ Munchen, Dr von Hauner Childrens Hosp, LMU Klinikum Munich, Div Pediat Neurol, Munich, Germany
[9] Ludwig Maximilians Univ Munchen, Dr von Hauner Childrens Hosp, LMU Ctr Children Med Complex, Munich, Germany
关键词
Botulinum neurotoxin A; Cerebral palsy; IncobotulinumtoxinA; Multipattern treatment; Pediatric; Spasticity; BOTULINUM TOXIN TREATMENT; SONOGRAPHY-GUIDED INJECTION; CHILDREN; SAFETY; PAIN; ADOLESCENTS; PREVALENCE; EQUINUS;
D O I
10.1016/j.pediatrneurol.2021.05.014
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Background: This randomized phase 3 study with double-blind main period (MP) and open-label extension (OLEX; NCT02002884) assessed incobotulinumtoxinA safety and efficacy for pediatric upper-limb spasticity treatment in ambulant/nonambulant (Gross Motor Function Classification System [GMFCS] I-V) patients, with the option of combined upper-and lower-limb treatment. Methods: Patients were aged two to 17 years with unilateral or bilateral spastic cerebral palsy (CP) and Ashworth Scale (AS) score >2 in treatment-selected clinical patterns. In the MP, patients were randomized (2:1:1) to incobotulinumtoxinA 8, 6, or 2 U/kg body weight (maximum 200, 150, 50 U/upper limb), with optional lower-limb injections in one of five topographical distributions (total body dose <16 to 20 U/kg, maximum 400 to 500 U, depending on body weight and GMFCS level). In the OLEX, patients received three further treatment cycles, at the highest MP doses (8 U/kg/upper limb group). Outcomes included AS, Global Impression of Change Scale (GICS), and adverse events (AEs). Results: AS scores improved from baseline to week 4 in all MP dose groups (n = 350); patients in the incobotulinumtoxinA 8 U/kg group had significantly greater spasticity improvements versus the 2 U/kg group (least-squares mean [standard error] for upper-limb main clinical target pattern-1.15 [0.06] versus-0.93 [0.08]; P = 0.017). Investigator's, child/adolescent's, and parent/caregiver's GICS scores showed improvements in all groups. Treatment benefits were sustained over further treatment cycles. AE incidence did not increase with dose or repeated treatment across GMFCS levels. Conclusions: Data provide evidence for sustained efficacy and safety of multipattern incobotulinumtoxinA treatment in children and adolescents with upper-limb spasticity. (c) 2021 The Authors. Published by Elsevier Inc. This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
引用
收藏
页码:10 / 20
页数:11
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