Syed Yahiya Y
Springer, Private Bag 65901, Mairangi Bay, Auckland, 0754, New Zealand.
Paediatr Drugs. 2017 Aug;19(4):367-373. doi: 10.1007/s40272-017-0242-4.
AbobotulinumtoxinA (Dysport) is currently the only botulinum toxin A formulation approved by the US FDA for the treatment of lower limb spasticity in pediatric patients aged ≥2 years. Intramuscular abobotulinumtoxinA was approved based on the results of a pivotal phase 3 trial in children with lower limb spasticity due to cerebral palsy. In this trial, a single treatment cycle with abobotulinumtoxinA 10-15 U/kg/leg injected into the gastrocnemius and soleus muscles significantly improved ankle plantar flexor muscle tone (primary endpoint), with abobotulinumtoxinA recipients showing a significant response to treatment relative to placebo. AbobotulinumtoxinA treatment also improved spasticity grade. The improvements in muscle tone and spasticity were associated with an improved ability to attain functional goals. Clinical benefits of abobotulinumtoxinA treatment lasted for 16-22 weeks in most patients, and were maintained with multiple treatment cycles during 1 year in an open-label extension study. AbobotulinumtoxinA was generally well tolerated, with a relatively low incidence of treatment-related adverse events. In summary, abobotulinumtoxinA is an effective and generally well tolerated treatment option for children with lower limb spasticity.
阿柏西普肉毒毒素A(得保松)是目前美国食品药品监督管理局(FDA)批准的唯一一种用于治疗≥2岁儿科患者下肢痉挛的肉毒毒素A制剂。肌肉注射阿柏西普肉毒毒素A的批准是基于一项针对因脑瘫导致下肢痉挛儿童的关键3期试验结果。在该试验中,将10 - 15 U/kg/腿的阿柏西普肉毒毒素A注射到腓肠肌和比目鱼肌中进行单周期治疗,显著改善了踝关节跖屈肌肌张力(主要终点),与安慰剂相比,接受阿柏西普肉毒毒素A治疗的患者对治疗有显著反应。阿柏西普肉毒毒素A治疗还改善了痉挛等级。肌张力和痉挛的改善与实现功能目标的能力提高相关。在大多数患者中,阿柏西普肉毒毒素A治疗的临床益处持续16 - 22周,并且在一项开放标签扩展研究中,在1年的多个治疗周期中得以维持。阿柏西普肉毒毒素A总体耐受性良好,与治疗相关的不良事件发生率相对较低。总之,阿柏西普肉毒毒素A是治疗下肢痉挛儿童的一种有效且总体耐受性良好的治疗选择。