A Randomized, Double-blind, Placebo-controlled Trial of Certolizumab Pegol in Women with Refractory Interstitial Cystitis/Bladder Pain Syndrome

被引:50
作者
Bosch, Philip C. [1 ,2 ]
机构
[1] Univ Calif San Diego, Med Ctr, Dept Urol, 225 Dickinson St, San Diego, CA 92103 USA
[2] Palomar Med Ctr, Dept Urol, Escondido, CA USA
关键词
Adalimumab; Autoimmune diseases; Bladder pain syndrome; Certolizumab pegol; Interstitial cystitis; Placebo effect; Tumor necrosis factor-alpha; TUMOR-NECROSIS-FACTOR; PENTOSAN POLYSULFATE; AUTOIMMUNE-DISEASES; CLINICAL-TRIAL; SYMPTOM-INDEX; MECHANISM; CRITERIA;
D O I
10.1016/j.eururo.2018.07.026
中图分类号
R5 [内科学]; R69 [泌尿科学(泌尿生殖系疾病)];
学科分类号
1002 ; 100201 ;
摘要
Background: Interstitial cystitis/bladder pain syndrome (IC/BPS) is a chronic, disabling bladder disease, with an uncertain pathophysiology and no universally effective treatment. Objective: To evaluate the efficacy and safety of certolizumab pegol compared with placebo in women with refractory IC/BPS. Design, setting, and participants: Eligiblewomen, aged 18-65 yr with moderate to severe IC/BPS, were enrolled in this randomized, double-blind, placebo-controlled pilot study. Intervention: Study patients were randomized at a 2: 1 ratio to receive either certolizumab pegol or placebo. Outcome measurements and statistical analysis: The primary outcome measure was a patient-reported global response assessment (GRA). Secondary endpoints included Interstitial Cystitis Symptom Index (ICSI), Interstitial Cystitis Problem Index (ICPI), and a numeric rating scale for pain and urgency. Results and limitations: The primary endpoint of GRA improvement at week 2 was not met. However, by week 18, there was significant improvement in GRA for certolizumab pegol compared with placebo in pain (odds ratio [OR] = 17.3, p = 0.002), urgency (OR = 9.92, p = 0.02), and overall symptoms (OR = 15.0, p = 0.006). At week 18, there was a statistically significant improvement for certolizumab pegol compared with placebo in change from baseline for ICSI of -3.6 (95% confidence interval [CI]: -6.9 to -0.29, p = 0.03), ICPI of -3.0 (95% CI: -6.1 to 0.12, p = 0.042), pain scale of -2.0 (95% CI: -3.9 to -0.15, p = 0.02), and urgency scale of -1.7 (95% CI: -3.5 to 0.06, p = 0.03). There was a significant difference in greater than 30% reduction in pain from baseline comparing certolizumab pegol with placebo at week 18 (OR = 13.0, p = 0.02). Limitations include a larger, longer, multicenter trial is warranted with phenotypic categorization of patients. Conclusions: Women with moderate to severe refractory IC/BPS were more likely to experience significant improvement in symptoms with certolizumab pegol compared with placebo therapy. Further investigation of certolizumab pegol for the treatment of IC/BPS is warranted with a larger, longer, multicenter, randomized, placebo-controlled trial. Patient summary: Women with moderate to severe interstitial cystitis/bladder pain syndrome were helped with a medication used to treat autoimmune diseases. (C) 2018 European Association of Urology. Published by Elsevier B.V. All rights reserved.
引用
收藏
页码:623 / 630
页数:8
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