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5%利多卡因药用贴剂与普瑞巴林治疗带状疱疹后神经痛和糖尿病性多发性神经病的开放标签、非劣效性两阶段随机对照试验研究

5% lidocaine medicated plaster versus pregabalin in post-herpetic neuralgia and diabetic polyneuropathy: an open-label, non-inferiority two-stage RCT study.

作者信息

Baron Ralf, Mayoral Victor, Leijon Göran, Binder Andreas, Steigerwald Ilona, Serpell Michael

机构信息

Division of Neurological Pain Research and Therapy, Department of Neurology, Universitätsklinikum Schleswig-Holstein, Campus Kiel, Kiel, Germany.

出版信息

Curr Med Res Opin. 2009 Jul;25(7):1663-76. doi: 10.1185/03007990903047880.

Abstract

OBJECTIVE

To compare efficacy and safety of 5% lidocaine medicated plaster with pregabalin in patients with post-herpetic neuralgia (PHN) or painful diabetic polyneuropathy (DPN).

STUDY DESIGN AND METHODS

This was a two-stage adaptive, randomized, open-label, multicentre, non-inferiority study. Data are reported from the initial 4-week comparative phase, in which adults with PHN or painful DPN received either topical 5% lidocaine medicated plaster applied to the most painful skin area or twice-daily pregabalin capsules titrated to effect according to the Summary of Product Characteristics. The primary endpoint was response rate at 4 weeks, defined as reduction averaged over the last three days from baseline of > or = 2 points or an absolute value of < or = 4 points on the 11-point Numerical Rating Scale (NRS-3). Secondary endpoints included 30% and 50% reductions in NRS-3 scores; change in allodynia severity rating; quality of life (QoL) parameters EQ-5D, CGIC, and PGIC; patient satisfaction with treatment; and evaluation of safety (laboratory parameters, vital signs, physical examinations, adverse events [AEs], drug-related AEs [DRAEs], and withdrawal due to AEs).

RESULTS

Ninety-six patients with PHN and 204 with painful DPN were analysed (full analysis set, FAS). Overall, 66.4% of patients treated with the 5% lidocaine medicated plaster and 61.5% receiving pregabalin were considered responders (corresponding numbers for the per protocol set, PPS: 65.3% vs. 62.0%). In PHN more patients responded to 5% lidocaine medicated plaster treatment than to pregabalin (PPS: 62.2% vs. 46.5%), while response was comparable for patients with painful DPN (PPS: 66.7% vs 69.1%). 30% and 50% reductions in NRS-3 scores were greater with 5% lidocaine medicated plaster than with pregabalin. Both treatments reduced allodynia severity. 5% lidocaine medicated plaster showed greater improvements in QoL based on EQ-5D in both PHN and DPN. PGIC and CGIC scores indicated greater improvement for 5% lidocaine medicated plaster treated patients with PHN. Improvements were comparable between treatments in painful DPN. Fewer patients administering 5% lidocaine medicated plaster experienced AEs (safety set, SAF: 18.7% vs. 46.4%), DRAEs (5.8% vs. 41.2%) and related discontinuations compared to patients taking pregabalin.

CONCLUSION

5% lidocaine medicated plaster showed better efficacy compared with pregabalin in patients with PHN. Within DPN, efficacy was comparable for both treatments. 5% lidocaine medicated plaster showed a favourable efficacy/safety profile with greater improvements in patient satisfaction and QoL compared with pregabalin for both indications, supporting its first line position in the treatment of localized neuropathic pain.

摘要

目的

比较5%利多卡因药用贴剂与普瑞巴林治疗带状疱疹后神经痛(PHN)或疼痛性糖尿病性多发性神经病变(DPN)患者的疗效和安全性。

研究设计与方法

这是一项两阶段适应性、随机、开放标签、多中心、非劣效性研究。数据来自最初为期4周的比较阶段,在此阶段,患有PHN或疼痛性DPN的成年人接受以下两种治疗之一:将5%利多卡因药用贴剂局部应用于最疼痛的皮肤区域,或根据产品特性摘要将普瑞巴林胶囊每日两次滴定至有效剂量。主要终点是4周时的缓解率,定义为在11点数字评定量表(NRS-3)上,从基线开始最后三天的平均降幅≥2分或绝对值≤4分。次要终点包括NRS-3评分降低30%和50%;痛觉过敏严重程度评级的变化;生活质量(QoL)参数EQ-5D、CGIC和PGIC;患者对治疗的满意度;以及安全性评估(实验室参数、生命体征、体格检查、不良事件[AEs]、药物相关不良事件[DRAEs]以及因AE导致的停药)。

结果

分析了96例PHN患者和204例疼痛性DPN患者(全分析集,FAS)。总体而言,使用5%利多卡因药用贴剂治疗的患者中有66.4%被视为缓解者,接受普瑞巴林治疗的患者中有61.5%被视为缓解者(符合方案集,PPS的相应数字分别为65.3%对62.0%)。在PHN患者中,对5%利多卡因药用贴剂治疗有反应的患者多于对普瑞巴林有反应的患者(PPS:62.2%对46.5%),而在疼痛性DPN患者中,两种治疗的反应相当(PPS:66.7%对69.1%)。5%利多卡因药用贴剂使NRS-3评分降低30%和50%的幅度大于普瑞巴林。两种治疗均降低了痛觉过敏的严重程度。基于EQ-5D,5%利多卡因药用贴剂在PHN和DPN患者中均显示出更大的生活质量改善。PGIC和CGIC评分表明,5%利多卡因药用贴剂治疗的PHN患者改善更大。在疼痛性DPN患者中,两种治疗的改善相当。与服用普瑞巴林的患者相比,使用5%利多卡因药用贴剂的患者发生AE(安全性集,SAF:18.7%对46.4%)、DRAEs(5.8%对41.2%)及相关停药的情况更少。

结论

与普瑞巴林相比,5%利多卡因药用贴剂在PHN患者中显示出更好的疗效。在DPN患者中,两种治疗的疗效相当。5%利多卡因药用贴剂显示出良好的疗效/安全性概况,与普瑞巴林相比,在两种适应症中患者满意度和生活质量均有更大改善,支持其在治疗局限性神经病理性疼痛中的一线地位。

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