首页> 外文期刊>The Journal of Urology >Clinical efficacy, safety and tolerability of collagenase clostridium histolyticum for the treatment of peyronie disease in 2 large double-blind, randomized, placebo controlled phase 3 studies
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Clinical efficacy, safety and tolerability of collagenase clostridium histolyticum for the treatment of peyronie disease in 2 large double-blind, randomized, placebo controlled phase 3 studies

机译:在2项大型双盲,随机,安慰剂对照的3期大型研究中,溶组织性梭状芽孢杆菌胶原酶治疗pyronyie疾病的临床疗效,安全性和耐受性

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Purpose: IMPRESS (Investigation for Maximal Peyronie's Reduction Efficacy and Safety Studies) I and II examined the clinical efficacy and safety of collagenase Clostridium histolyticum intralesional injections in subjects with Peyronie disease. Co-primary outcomes in these identical phase 3 randomized, double-blind, placebo controlled studies included the percent change in the penile curvature abnormality and the change in the Peyronie disease questionnaire symptom bother score from baseline to 52 weeks. Materials and Methods: IMPRESS I and II examined collagenase C. histolyticum intralesional injections in 417 and 415 subjects, respectively, through a maximum of 4 treatment cycles, each separated by 6 weeks. Men received up to 8 injections of 0.58 mg collagenase C. histolyticum, that is 2 injections per cycle separated by approximately 24 to 72 hours with the second injection of each followed 24 to 72 hours later by penile plaque modeling. Men were stratified by baseline penile curvature (30 to 60 vs 61 to 90 degrees) and randomized to collagenase C. histolyticum or placebo 2:1 in favor of the former. Results: Post hoc meta-analysis of IMPRESS I and II data revealed that men treated with collagenase C. histolyticum showed a mean 34% improvement in penile curvature, representing a mean ± SD -17.0 ± 14.8 degree change per subject, compared with a mean 18.2% improvement in placebo treated men, representing a mean -9.3 ± 13.6 degree change per subject (p <0.0001). The mean change in Peyronie disease symptom bother score was significantly improved in treated men vs men on placebo (-2.8 ± 3.8 vs -1.8 ± 3.5, p = 0.0037). Three serious adverse events (corporeal rupture) were surgically repaired. Conclusions: IMPRESS I and II support the clinical efficacy and safety of collagenase C. histolyticum for the physical and psychological aspects of Peyronie disease.
机译:目的:IMPRESS(最大的Peyronie降低功效和安全性研究的研究)I和II检查了Peyronie病患者胶原酶溶组织梭状芽胞杆菌病灶内注射的临床疗效和安全性。这些相同的第3阶段随机,双盲,安慰剂对照研究的共同主要结果包括从基线到52周阴茎弯曲异常的百分比变化和Peyronie疾病问卷症状困扰评分的变化。材料和方法:IMPRESS I和II通过最多4个治疗周期(分别间隔6周)分别检查了417和415位受试者的溶酶解组织梭状芽胞杆菌的病灶内注射。男性最多接受8次注射0.58 mg的组织酶梭状芽胞杆菌,即每个周期2次注射,间隔约24至72小时,第二次注射两次,然后在24至72小时后进行阴茎斑块建模。将男性按基线阴茎弯曲度(30至60与61至90度)进行分层,并随机分配至胶原酶溶组织梭状芽胞杆菌或安慰剂2:1,以有利于前者。结果:IMPRESS I和II数据的事后荟萃分析显示,用胶原酶溶组织梭状芽胞杆菌治疗的男性平均阴茎弯曲度提高了34%,与平均水平相比,每位受试者的平均变化为±SD -17.0±14.8度经安慰剂治疗的男性改善了18.2%,表示每个受试者的平均变化幅度为-9.3±13.6(p <0.0001)。接受治疗的男性与接受安慰剂的男性相比,佩罗尼氏病症状困扰评分的平均变化得到了显着改善(-2.8±3.8与-1.8±3.5,p = 0.0037)。手术修复了三个严重的不良事件(体破裂)。结论:IMPRESS I和II支持溶酶胶原组织梭状芽胞杆菌在Peyronie疾病的生理和心理方面的临床疗效和安全性。

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