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

被引:34
|
作者
Nickel, J. Curtis [1 ]
Mills, Ian W. [2 ]
Crook, Tim J. [2 ]
Jorga, Anamaria [3 ]
Smith, Michael D. [3 ]
Atkinson, Gary [2 ]
Krieger, John N. [4 ]
机构
[1] Queens Univ, Kingston, ON, Canada
[2] Pfizer Ltd, Tadworth, Surrey, England
[3] Pfizer Inc, New York, NY USA
[4] Univ Washington, Seattle, WA 98195 USA
来源
JOURNAL OF UROLOGY | 2016年 / 195卷 / 04期
关键词
cystitis; interstitial; pelvic pain; prostatitis; nerve growth factor; tanezumab; NERVE GROWTH-FACTOR; PROOF-OF-CONCEPT; URINARY-BLADDER; SYMPTOM INDEX; DOUBLE-BLIND; EFFICACY; SAFETY; TRIAL; KNEE; OSTEOARTHRITIS;
D O I
10.1016/j.juro.2015.10.178
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
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 mg/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.
引用
收藏
页码:942 / 948
页数:7
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