International Consultation on Interstitial Cystitis Japan, Kyoto, Japan.
Japanese Red Cross Medical Center, Tokyo, Japan.
Int J Urol. 2019 Jun;26 Suppl 1:4-11. doi: 10.1111/iju.13968.
Suplatast tosilate, a Th2 cytokine inhibitor, was predicted to relieve interstitial cystitis symptoms. Four studies with suplatast tosilate in Japanese interstitial cystitis patients have been conducted: a single-arm clinical study, a phase II dose-ranging trial, a phase III trial with placebo, and a second phase PIII trial with placebo. Treatment efficacy was observed in the first two studies; however, in the phase PIII trials, no significant difference in interstitial cystitis symptom score changes was observed between suplatast tosilate and placebo. We summarized these four studies to investigate factors causing the difference in observed efficacy.
Placebo effects in the first two studies and differences regarding study design between the four studies were considered to be possible factors. Therefore, placebo effects were investigated by comparing interstitial cystitis symptom score changes, and the study designs were compared to investigate the effects on observed efficacy.
Interstitial cystitis symptom score changes in the phase PII treatment groups increased in a dose-dependent manner and showed an almost linear relationship with interstitial cystitis symptom score changes observed in placebo groups of 2 phase PIII studies. A major difference regarding the phase PIII study design was the use of diagnostic hydrodistention. Diagnostic hydrodistention and its washout period were applied only in the phase PIII trials.
Comparison of interstitial cystitis symptom score changes suggested that the placebo effect was very small. Use of diagnostic hydrodistention was considered to be a major difference in the population characteristics of the studies and may have resulted in different observed efficacies. Diagnostic hydrodistention, which potentially influences the treatment effect, is probably not essential for trials of suplatast in interstitial cystitis patients.
噻托溴铵是一种 Th2 细胞因子抑制剂,预计能缓解间质性膀胱炎症状。已经在日本间质性膀胱炎患者中进行了四项噻托溴铵研究:一项单臂临床研究、一项剂量范围 II 期试验、一项安慰剂对照 III 期试验和第二项安慰剂对照 III 期试验。在前两项研究中观察到了治疗效果;然而,在 III 期试验中,噻托溴铵与安慰剂之间在间质性膀胱炎症状评分变化方面没有观察到显著差异。我们总结了这四项研究,以探讨导致观察到的疗效差异的因素。
考虑到前两项研究中的安慰剂效应以及四项研究之间的研究设计差异可能是造成疗效差异的因素,因此通过比较间质性膀胱炎症状评分变化来研究安慰剂效应,并比较研究设计以研究其对观察到的疗效的影响。
II 期治疗组的间质性膀胱炎症状评分变化呈剂量依赖性增加,并且与两项 III 期研究的安慰剂组的间质性膀胱炎症状评分变化几乎呈线性关系。III 期研究设计的一个主要差异是使用了诊断性膀胱扩张术。诊断性膀胱扩张术及其冲洗期仅在 III 期试验中使用。
比较间质性膀胱炎症状评分变化表明安慰剂效应很小。使用诊断性膀胱扩张术被认为是研究人群特征的一个主要差异,可能导致了不同的观察疗效。诊断性膀胱扩张术可能会影响治疗效果,因此对于噻托溴铵治疗间质性膀胱炎患者的试验来说可能不是必需的。