DeLong Jessica, Virasoro Ramón, Pichardo Merycarla, Estrella Rafael, Rodríguez Lay Ramón, Espino Gustavo, Elliott Sean
MultiCare Urology, Puyallup, Washington.
University of Colorado, Colorado Springs, Colorado.
J Urol. 2025 Jan;213(1):90-98. doi: 10.1097/JU.0000000000004229. Epub 2024 Aug 30.
We report the 5-year study closeout results for the ROBUST I trial evaluating the safety and efficacy of the Optilume drug-coated balloon (DCB) for men with short, recurrent bulbar urethral strictures.
Adult men with recurrent bulbar urethral strictures ≤ 2 cm long and lumen < 12F were included in the study and treated with the Optilume DCB. Outcome measures included symptom questionnaires, maximum urinary flow rate, postvoid residual, and freedom from repeat intervention. Functional success was defined as improvement in International Prostate Symptom Score ≥ 50% without re-treatment.
Fifty-three men were enrolled and treated, and 31 subjects completed all follow-up. Functional success was achieved in 58% (25/43) patients at 5 years. Average International Prostate Symptom Score improved from a mean of 25.2 at baseline to 7.2 at 5 years ( < .001). Freedom from repeat intervention was maintained through 5 years at 71.7% estimated by Kaplan-Meier. Maximum urinary flow rate improved from 5.0 mL/s at baseline to 19.9 ( < .01), and average postvoid residual was reduced from 141.4 mL to 59.5 mL ( < .01) at 5 years of follow-up. Erectile function remained unaffected. There were no serious treatment-related adverse events.
In this challenging cohort of men with failed prior endoscopic treatment, the Optilume DCB shows sustained improvement in subjective and objective voiding parameters at 5 years. Optilume is a safe and effective treatment option for appropriately selected men with recurrent bulbar urethral stricture who wish to avoid urethroplasty. Results are in line with the ROBUST III randomized controlled trial that will continue follow-up through 5 years.
CLINICAL TRIAL NO.: NCT03014726.
我们报告了ROBUST I试验的5年研究结束结果,该试验评估了Optilume药物涂层球囊(DCB)治疗男性短段复发性球部尿道狭窄的安全性和有效性。
纳入复发性球部尿道狭窄长度≤2 cm且管腔<12F的成年男性,并使用Optilume DCB进行治疗。观察指标包括症状问卷、最大尿流率、残余尿量以及无需再次干预。功能成功定义为国际前列腺症状评分改善≥50%且无需再次治疗。
53名男性入组并接受治疗,31名受试者完成了所有随访。5年时,58%(25/43)的患者获得功能成功。国际前列腺症状评分平均从基线时的25.2改善至5年时的7.2(P<0.001)。通过Kaplan-Meier估计,5年内无需再次干预的比例维持在71.7%。最大尿流率从基线时的5.0 mL/s改善至19.9(P<0.01),随访5年时平均残余尿量从141.4 mL降至59.5 mL(P<0.01)。勃起功能未受影响。未发生严重的治疗相关不良事件。
在这一先前内镜治疗失败的具有挑战性的男性队列中,Optilume DCB在5年时显示出主观和客观排尿参数的持续改善。对于希望避免尿道成形术的适当选择的复发性球部尿道狭窄男性,Optilume是一种安全有效的治疗选择。结果与将继续随访5年的ROBUST III随机对照试验一致。
NCT03014726。