肉毒杆菌毒素a使用2毫升稀释剂(500 U/2毫升)在多个治疗周期中保持持久的改善。

Journal of Clinical Movement Disorders Pub Date : 2020-08-31 eCollection Date: 2020-01-01 DOI:10.1186/s40734-020-00090-x
Khashayar Dashtipour, Stefan Wietek, Bruce Rubin, Pascal Maisonobe, Laxman Bahroo, Richard Trosch
{"title":"肉毒杆菌毒素a使用2毫升稀释剂(500 U/2毫升)在多个治疗周期中保持持久的改善。","authors":"Khashayar Dashtipour,&nbsp;Stefan Wietek,&nbsp;Bruce Rubin,&nbsp;Pascal Maisonobe,&nbsp;Laxman Bahroo,&nbsp;Richard Trosch","doi":"10.1186/s40734-020-00090-x","DOIUrl":null,"url":null,"abstract":"<p><strong>Background: </strong>Cervical dystonia (CD), the most common focal dystonia, is a chronic neurological movement disorder characterized by sustained involuntary contractions of the neck muscles, leading to abnormal postures. AbobotulinumtoxinA (aboBoNT-A) was approved in the US initially as a 500 U per 1-mL dilution and subsequently, as a 500 U/2-mL dilution (or 250 U/mL), thereby providing clinicians with more flexible dosing options to better meet individual patient needs. The objective of this open-label extension study was to evaluate the longer term safety and efficacy of repeat treatments with aboBoNT-A using 2-mL dilutions in adults with cervical dystonia.</p><p><strong>Methods: </strong>Patients (<i>N</i> = 112) from a 12-week, double-blind lead-in study (NCT01753310) received up to three additional treatments of aboBoNT-A, with re-treatment every 12-16 weeks based on clinical judgment. Safety was assessed through treatment-emergent adverse events (TEAEs). The Toronto Western Spasmodic Torticollis Rating Scale (TWSTRS) total and subscale scores were measured at day 1 of each treatment cycle (C), 4 weeks after each treatment, and 12 weeks after the third treatment. Descriptive statistics were used for all analyses.</p><p><strong>Results: </strong>In cycles 1, 2, 3, and 4, respectively, 35.7, 25.9, 30.2, and 22.8% of patients reported TEAEs. Dysphagia, muscular weakness, and neck pain were each reported by 10.7% of patients, over the full study duration. Mean TWSTRS total score decreased from 37.7 (SD 13.6 [C1, day 1]) to 30.1 (SD 12.8 [C3, week 12]). In each cycle, TWSTRS total and subscale scores decreased from day 1 to week 4 and increased between weeks 4 and 12, though the week 12 scores remained lower than day 1 scores.</p><p><strong>Conclusion: </strong>Extended treatment of cervical dystonia with aboBoNT-A (up to 3 additional treatment cycles) using a 2-mL dilution is effective, with a positive risk-benefit profile.</p><p><strong>Trial registration: </strong>ClinicalTrials.gov Identifier: NCT01753336. Registered 17 Dec 2012.</p>","PeriodicalId":15374,"journal":{"name":"Journal of Clinical Movement Disorders","volume":null,"pages":null},"PeriodicalIF":0.0000,"publicationDate":"2020-08-31","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1186/s40734-020-00090-x","citationCount":"2","resultStr":"{\"title\":\"AbobotulinumtoxinA using 2-mL dilution (500 U/2-mL) maintains durable improvement across multiple treatment cycles.\",\"authors\":\"Khashayar Dashtipour,&nbsp;Stefan Wietek,&nbsp;Bruce Rubin,&nbsp;Pascal Maisonobe,&nbsp;Laxman Bahroo,&nbsp;Richard Trosch\",\"doi\":\"10.1186/s40734-020-00090-x\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><strong>Background: </strong>Cervical dystonia (CD), the most common focal dystonia, is a chronic neurological movement disorder characterized by sustained involuntary contractions of the neck muscles, leading to abnormal postures. AbobotulinumtoxinA (aboBoNT-A) was approved in the US initially as a 500 U per 1-mL dilution and subsequently, as a 500 U/2-mL dilution (or 250 U/mL), thereby providing clinicians with more flexible dosing options to better meet individual patient needs. The objective of this open-label extension study was to evaluate the longer term safety and efficacy of repeat treatments with aboBoNT-A using 2-mL dilutions in adults with cervical dystonia.</p><p><strong>Methods: </strong>Patients (<i>N</i> = 112) from a 12-week, double-blind lead-in study (NCT01753310) received up to three additional treatments of aboBoNT-A, with re-treatment every 12-16 weeks based on clinical judgment. Safety was assessed through treatment-emergent adverse events (TEAEs). The Toronto Western Spasmodic Torticollis Rating Scale (TWSTRS) total and subscale scores were measured at day 1 of each treatment cycle (C), 4 weeks after each treatment, and 12 weeks after the third treatment. Descriptive statistics were used for all analyses.</p><p><strong>Results: </strong>In cycles 1, 2, 3, and 4, respectively, 35.7, 25.9, 30.2, and 22.8% of patients reported TEAEs. Dysphagia, muscular weakness, and neck pain were each reported by 10.7% of patients, over the full study duration. Mean TWSTRS total score decreased from 37.7 (SD 13.6 [C1, day 1]) to 30.1 (SD 12.8 [C3, week 12]). In each cycle, TWSTRS total and subscale scores decreased from day 1 to week 4 and increased between weeks 4 and 12, though the week 12 scores remained lower than day 1 scores.</p><p><strong>Conclusion: </strong>Extended treatment of cervical dystonia with aboBoNT-A (up to 3 additional treatment cycles) using a 2-mL dilution is effective, with a positive risk-benefit profile.</p><p><strong>Trial registration: </strong>ClinicalTrials.gov Identifier: NCT01753336. Registered 17 Dec 2012.</p>\",\"PeriodicalId\":15374,\"journal\":{\"name\":\"Journal of Clinical Movement Disorders\",\"volume\":null,\"pages\":null},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2020-08-31\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://sci-hub-pdf.com/10.1186/s40734-020-00090-x\",\"citationCount\":\"2\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Journal of Clinical Movement Disorders\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.1186/s40734-020-00090-x\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"2020/1/1 0:00:00\",\"PubModel\":\"eCollection\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of Clinical Movement Disorders","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1186/s40734-020-00090-x","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2020/1/1 0:00:00","PubModel":"eCollection","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 2

摘要

背景:颈肌张力障碍(CD)是最常见的局灶性肌张力障碍,是一种慢性神经运动障碍,其特征是颈部肌肉持续不自主收缩,导致异常姿势。AbobotulinumtoxinA (aboBoNT-A)最初在美国被批准为500 U/ 1ml稀释,随后被批准为500 U/ 2ml稀释(或250 U/mL),从而为临床医生提供更灵活的剂量选择,以更好地满足个体患者的需求。这项开放标签扩展研究的目的是评估使用2毫升稀释aboBoNT-A重复治疗宫颈张力障碍成人患者的长期安全性和有效性。方法:来自一项为期12周的双盲先导研究(NCT01753310)的患者(N = 112)接受了最多3次额外的aboBoNT-A治疗,根据临床判断每12-16周重新治疗一次。通过治疗中出现的不良事件(teae)来评估安全性。在每个治疗周期的第1天(C)、每次治疗后4周和第三次治疗后12周测量多伦多西部痉挛性斜颈评定量表(TWSTRS)总评分和亚量表评分。所有分析均采用描述性统计。结果:在第1、2、3和4个周期中,分别有35.7%、25.9%、30.2和22.8%的患者报告了teae。在整个研究期间,10.7%的患者分别报告了吞咽困难、肌肉无力和颈部疼痛。TWSTRS平均总分从37.7分(SD 13.6 [C1,第1天])降至30.1分(SD 12.8 [C3,第12周])。在每个周期中,TWSTRS总得分和分量表得分从第1天到第4周下降,在第4周到第12周上升,但第12周的得分仍然低于第1天的得分。结论:使用2 ml稀释剂延长aboBoNT-A治疗宫颈肌张力障碍(最多3个额外治疗周期)是有效的,具有积极的风险-收益特征。试验注册:ClinicalTrials.gov标识符:NCT01753336。注册于2012年12月17日。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

AbobotulinumtoxinA using 2-mL dilution (500 U/2-mL) maintains durable improvement across multiple treatment cycles.

AbobotulinumtoxinA using 2-mL dilution (500 U/2-mL) maintains durable improvement across multiple treatment cycles.

AbobotulinumtoxinA using 2-mL dilution (500 U/2-mL) maintains durable improvement across multiple treatment cycles.

AbobotulinumtoxinA using 2-mL dilution (500 U/2-mL) maintains durable improvement across multiple treatment cycles.

Background: Cervical dystonia (CD), the most common focal dystonia, is a chronic neurological movement disorder characterized by sustained involuntary contractions of the neck muscles, leading to abnormal postures. AbobotulinumtoxinA (aboBoNT-A) was approved in the US initially as a 500 U per 1-mL dilution and subsequently, as a 500 U/2-mL dilution (or 250 U/mL), thereby providing clinicians with more flexible dosing options to better meet individual patient needs. The objective of this open-label extension study was to evaluate the longer term safety and efficacy of repeat treatments with aboBoNT-A using 2-mL dilutions in adults with cervical dystonia.

Methods: Patients (N = 112) from a 12-week, double-blind lead-in study (NCT01753310) received up to three additional treatments of aboBoNT-A, with re-treatment every 12-16 weeks based on clinical judgment. Safety was assessed through treatment-emergent adverse events (TEAEs). The Toronto Western Spasmodic Torticollis Rating Scale (TWSTRS) total and subscale scores were measured at day 1 of each treatment cycle (C), 4 weeks after each treatment, and 12 weeks after the third treatment. Descriptive statistics were used for all analyses.

Results: In cycles 1, 2, 3, and 4, respectively, 35.7, 25.9, 30.2, and 22.8% of patients reported TEAEs. Dysphagia, muscular weakness, and neck pain were each reported by 10.7% of patients, over the full study duration. Mean TWSTRS total score decreased from 37.7 (SD 13.6 [C1, day 1]) to 30.1 (SD 12.8 [C3, week 12]). In each cycle, TWSTRS total and subscale scores decreased from day 1 to week 4 and increased between weeks 4 and 12, though the week 12 scores remained lower than day 1 scores.

Conclusion: Extended treatment of cervical dystonia with aboBoNT-A (up to 3 additional treatment cycles) using a 2-mL dilution is effective, with a positive risk-benefit profile.

Trial registration: ClinicalTrials.gov Identifier: NCT01753336. Registered 17 Dec 2012.

求助全文
通过发布文献求助,成功后即可免费获取论文全文。 去求助
来源期刊
自引率
0.00%
发文量
0
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术官方微信