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替扎尼定可减轻间质性膀胱炎/膀胱疼痛综合征女性患者和伴有非神经相关躯体综合征患者的疼痛。

Tanezumab Reduces Pain in Women with Interstitial Cystitis/Bladder Pain Syndrome and Patients with Nonurological Associated Somatic Syndromes.

机构信息

Queen's University, Kingston, Ontario, Canada.

Pfizer Ltd, Tadworth, Surrey, United Kingdom.

出版信息

J Urol. 2016 Apr;195(4 Pt 1):942-8. doi: 10.1016/j.juro.2015.10.178. Epub 2015 Nov 11.

Abstract

PURPOSE

We performed pooled analyses from 3 small, clinical trials of tanezumab in patients with urological chronic pelvic pain, including chronic prostatitis/chronic pelvic pain syndrome and interstitial cystitis/bladder pain syndrome, to identify patient subpopulations more likely to benefit from tanezumab treatment.

MATERIALS AND METHODS

Pooled analyses included data from 208 patients with interstitial cystitis/bladder pain syndrome or chronic prostatitis/chronic pelvic pain syndrome randomized to placebo (104, 65 [62.5%] female) or tanezumab (104, 63 [60.6%] female) who received 1 dose or more of study medication. Data on tanezumab were from study A4091010 (interstitial cystitis/bladder pain syndrome) on 200 μg/kg intravenous, study A4091019 (chronic prostatitis/chronic pelvic pain syndrome) on 20 mg intravenous and study A4091035 (interstitial cystitis/bladder pain syndrome) on 20 mg subcutaneous. Primary study end points were evaluated using analysis of covariance with gender, study and baseline pain as covariates.

RESULTS

For pooled analyses least squares mean (SE) change from baseline in 24-hour pain intensity vs placebo was -0.60 (0.24, 90% CI -0.99, -0.20) overall and -0.99 (0.32, p=0.002) and -0.17 (0.36, p=0.650) for females and males, respectively. The improvement in pain intensity was significant (p=0.011) for patients with symptoms suggesting the concomitant presence of nonurological associated somatic syndromes but not for those with pelvic pain symptoms only (p=0.507).

CONCLUSIONS

Women with interstitial cystitis/bladder pain syndrome and patients with symptoms suggesting the concomitant presence of nonurological associated somatic syndromes were more likely to experience significant pain reduction with tanezumab than with placebo therapy. In contrast, no difference was reported in response between tanezumab and placebo therapy for men with chronic prostatitis/chronic pelvic pain syndrome symptoms only.

摘要

目的

我们对三项小型坦尼珠单抗治疗泌尿系统慢性盆腔疼痛(包括慢性前列腺炎/慢性盆腔疼痛综合征和间质性膀胱炎/膀胱疼痛综合征)的临床试验进行了汇总分析,以确定更有可能从坦尼珠单抗治疗中获益的患者亚组。

材料和方法

汇总分析包括来自 208 例间质性膀胱炎/膀胱疼痛综合征或慢性前列腺炎/慢性盆腔疼痛综合征患者的数据,这些患者随机分配至安慰剂(104 例,65 例[62.5%]为女性)或坦尼珠单抗(104 例,63 例[60.6%]为女性),这些患者接受了 1 次或更多次研究药物治疗。坦尼珠单抗的数据来自 A4091010 研究(间质性膀胱炎/膀胱疼痛综合征,静脉注射 200μg/kg)、A4091019 研究(慢性前列腺炎/慢性盆腔疼痛综合征,静脉注射 20mg)和 A4091035 研究(间质性膀胱炎/膀胱疼痛综合征,皮下注射 20mg)。主要研究终点采用协方差分析进行评估,性别、研究和基线疼痛为协变量。

结果

在汇总分析中,与安慰剂相比,24 小时疼痛强度的最小二乘均值(SE)变化为-0.60(0.24,90%CI-0.99,-0.20),女性为-0.99(0.32,p=0.002),男性为-0.17(0.36,p=0.650)。疼痛强度的改善具有统计学意义(p=0.011),对于有非泌尿系统相关躯体综合征同时存在症状的患者,但对于仅盆腔疼痛症状的患者则无统计学意义(p=0.507)。

结论

间质性膀胱炎/膀胱疼痛综合征的女性患者和有非泌尿系统相关躯体综合征同时存在症状的患者,与安慰剂治疗相比,更有可能经历显著的疼痛缓解。相比之下,对于仅患有慢性前列腺炎/慢性盆腔疼痛综合征症状的男性患者,坦尼珠单抗与安慰剂治疗之间的反应无差异。

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