Changes in the Effects of Peyronie's Disease After Treatment With Collagenase Clostridium histolyticum: Male Patients and Their Female Partners

被引:28
|
作者
Goldstein, Irwin [1 ]
Knoll, L. Dean [2 ]
Lipshultz, Larry I. [3 ]
Smith, Ted [4 ]
Kaufman, Gregory J. [5 ]
McMahon, Chris G. [6 ]
机构
[1] Alvarado Hosp, Sexual Med, 5555 Reservoir Dr,Suite 300, San Diego, CA 92120 USA
[2] Ctr Urol Treatment, Nashville, TN USA
[3] Baylor Coll Med, Scott Dept Urol, Houston, TX 77030 USA
[4] Endo Pharmaceut, Malvern, PA USA
[5] Auxilium Pharmaceut, Malvern, PA USA
[6] Australian Ctr Sexual Hlth, St Leonards, NSW, Australia
来源
SEXUAL MEDICINE | 2017年 / 5卷 / 02期
关键词
Collagenase; Efficacy; Peyronie's Disease; Sexual Partners; Female Sexual Function Index; INTRALESIONAL INTERFERON-ALPHA-2B; ERECTILE DYSFUNCTION; SURGICAL-TREATMENT; SAFETY; INJECTION; DISTRESS; EFFICACY; PHASE-3; IMPACT; BLIND;
D O I
10.1016/j.esxm.2017.02.001
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Introduction: Collagenase Clostridium histolyticum (CCH) intralesional injection was efficacious for the management of Peyronie's disease (PD) in the double-blinded, randomized, placebo-controlled Investigation for Maximal Peyronie's Reduction Efficacy and Safety Studies I and II (IMPRESS I and II). Little is known about the consequences of PD or treatment on the sexual partners of affected men. Aim: To assess the safety and efficacy of CCH treatment in men who received placebo in the IMPRESS I or II study and to evaluate the men's PD symptoms and partner bother as reported by female sexual partners. Methods: In this phase 3, open-label study (NCT01685437), men (n = 189) received up to eight injections of CCH (0.58 mg/injection). Female sexual partners who provided informed consent at screening (n = 30) participated in the study. Main Outcome Measures: Co-primary end points were change or percentage of change in penile curvature deformity and change in PD symptom bother domain score of the Peyronie's Disease Questionnaire (PDQ) from baseline to week 36. Participating women completed the PDQ for female sexual partners (PDQ-FSP) and the Female Sexual Function Index (FSFI). Results: Statistically significant mean improvements were observed in penile curvature deformity (36.3% decrease; 95% CI = -41.6 to -30.9) and PDQ symptom bother score (2.4-point decrease; 95% CI = - 3.0 to -1.8) from baseline to week 36. Most treatment-emergent adverse events were mild or moderate. After CCH treatment of their male partners, female sexual partners reported improvement (using the PDQ-FSP) in their male partner's PD symptoms and female bother regarding their partner's PD. The percentage of female sexual partners with sexual dysfunction (FSFI total score <= 26.55) also decreased after male partner treatment, from 75.0% at baseline to 33.3%. Conclusions: These results support the safety and efficacy of CCH in the management of appropriate patients with PD and the potential benefits for patients' partners. Copyright (C) 2017, The Authors. Published by Elsevier Inc. on behalf of the International Society for Sexual Medicine. This is an open access article under the CC BY-NC-ND license.
引用
收藏
页码:E124 / E130
页数:7
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