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一项前瞻性、多中心、双盲、随机临床试验,研究脂质体配方奥昔布宁毒素 A 膀胱灌注治疗间质性膀胱炎/膀胱疼痛综合征。

A Prospective, Multicenter, Double-Blind, Randomized Trial of Bladder Instillation of Liposome Formulation OnabotulinumtoxinA for Interstitial Cystitis/Bladder Pain Syndrome.

机构信息

Department of Urology, Kaohsiung Chang Gang Memorial Hospital, College of Medicine, Chang Gung University, Hualien, Taiwan; Department of Urology, Buddhist Tzu Chi General Hospital and Tzu Chi University, Hualien (HCK), Taiwan.

Department of Urology, Kaohsiung Chang Gang Memorial Hospital, College of Medicine, Chang Gung University, Hualien, Taiwan; Department of Urology, Buddhist Tzu Chi General Hospital and Tzu Chi University, Hualien (HCK), Taiwan.

出版信息

J Urol. 2017 Aug;198(2):376-382. doi: 10.1016/j.juro.2017.02.021. Epub 2017 Feb 12.

Abstract

PURPOSE

Intravesical instillation of liposomal formulated botulinum toxin A (lipotoxin) has shown therapeutic effects as treatment of refractory overactive bladder without needle injections. We assessed lipotoxin to treat refractory interstitial cystitis/bladder pain syndrome.

MATERIALS AND METHODS

This 2-center, double-blind, randomized, placebo controlled, physician initiated study enrolled patients with refractory interstitial cystitis/bladder pain syndrome. A total of 31 patients were assigned to intravesical instillation of lipotoxin (onabotulinumtoxinA 200 U with 80 mg sphingomyelin), 28 were assigned to onabotulinumtoxinA 200 U in normal saline and 31 were assigned to normal saline alone. The primary end point was the average change in O'Leary-Sant symptom scores, including ICSI (Interstitial Cystitis Symptom Index) and ICPI (Interstitial Cystitis Problem Index) between baseline and 4 weeks after treatment. Other end points included the average changes in a 3-day voiding diary, a visual analog scale for pain and a global response assessment of patient satisfaction.

RESULTS

Improvements in the pain scale and O'Leary-Sant symptom scores occurred in all 3 groups by 4 weeks after treatment. Lipotoxin instillation was associated with a statistically significant decrease in O'Leary-Sant symptom scores (mean ± SD 7.38 ± 8.75), ICSI (4.00 ± 4.28), ICPI (3.35 ± 5.11) and the visual analog scale pain scale (1.64 ± 2.52), and an increase in the global response assessment (1.35 ± 1.28). However, there was no difference in improvement among the 3 groups. No significant adverse events were found in any group.

CONCLUSIONS

Lipotoxin failed to demonstrate a positive proof of concept compared to onabotulinumtoxinA or placebo. However, a single intravesical instillation of lipotoxin was associated with decreased interstitial cystitis/bladder pain syndrome symptoms compared to baseline in patients with moderate to severe interstitial cystitis/bladder pain syndrome. The effect was likely due to a significant placebo effect.

摘要

目的

膀胱内注射脂质体包裹的肉毒毒素 A(脂质毒素)已被证明可通过非针注射治疗难治性逼尿过度症,具有治疗作用。我们评估了脂质毒素治疗难治性间质性膀胱炎/膀胱疼痛综合征的效果。

材料和方法

这是一项 2 中心、双盲、随机、安慰剂对照、医生发起的研究,招募了难治性间质性膀胱炎/膀胱疼痛综合征患者。共 31 例患者被分配至膀胱内注入脂质毒素(200 U 型肉毒毒素 A 加 80 mg 鞘磷脂),28 例患者被分配至生理盐水 200 U 型肉毒毒素 A,31 例患者被分配至单独生理盐水。主要终点是治疗后 4 周时 O'Leary-Sant 症状评分(包括 ICSI(间质性膀胱炎症状指数)和 ICPI(间质性膀胱炎问题指数))的平均变化。其他终点包括 3 天排尿日记、疼痛视觉模拟评分和患者满意度的整体反应评估的平均变化。

结果

治疗后 4 周时,所有 3 组的疼痛评分和 O'Leary-Sant 症状评分均有所改善。脂质毒素灌注与 O'Leary-Sant 症状评分(均值 ± 标准差 7.38 ± 8.75)、ICSI(4.00 ± 4.28)、ICPI(3.35 ± 5.11)和疼痛视觉模拟评分(1.64 ± 2.52)的统计学显著下降以及整体反应评估(1.35 ± 1.28)的增加相关。然而,3 组之间的改善没有差异。任何一组均未发现明显不良事件。

结论

与肉毒毒素 A 或安慰剂相比,脂质毒素未能证明积极的概念验证。然而,与基线相比,在中重度间质性膀胱炎/膀胱疼痛综合征患者中,单次膀胱内注射脂质毒素与间质性膀胱炎/膀胱疼痛综合征症状的减少相关。这种作用可能是由于显著的安慰剂效应。

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