Optilume drug-coated balloon for anterior urethral stricture: 2-year results of the ROBUST III trial

IF 1.6 Q3 UROLOGY & NEPHROLOGY BJUI compass Pub Date : 2023-12-18 DOI:10.1002/bco2.312
Maia E. VanDyke, Allen F. Morey, Karl Coutinho, Kaiser J. Robertson, Richard D'Anna, Kent Chevli, Christopher H. Cantrill, Michael J. Ehlert, Alexis E. Te, Jeffrey Dann, Jessica M. DeLong, Ramón Virasoro, Judith C. Hagedorn, Richard Levin, Euclid DeSouza, David DiMarco, Brad A. Erickson, Carl Olsson, Sean P. Elliott
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Abstract

Objective

The aim of this study is to report the updated 2-year results of the intervention arm of the ROBUST III randomized trial evaluating the safety and efficacy of the Optilume drug-coated balloon (DCB) versus standard endoscopic management of recurrent male anterior urethral stricture.

Materials and Methods

Eligible patients included men with recurrent anterior urethral stricture ≤3 cm in length and ≤12Fr in diameter, International Prostate Symptom Score (IPSS) ≥11 and peak flow rate (Qmax) <15 mL/s. Patients were randomized to treatment with the Optilume DCB or standard-of-care endoscopic management. Primary efficacy endpoints measured at 2 years included freedom from re-intervention and changes in IPSS, Qmax and post-void residual (PVR). Secondary endpoint was impact on sexual function using the International Index of Erectile Function (IIEF). Primary safety endpoint was freedom from serious procedure- or device-related adverse events (AEs).

Results

A total of 127 patients enrolled at 22 sites in the United States and Canada (48 randomized to standard-of-care dilation and 79 to DCB dilation). Seventy-five patients in the DCB arm entered the open-label phase after 6 months. Participants averaged 3.2 prior endoscopic interventions (range 2–10); most (89.9%) had bulbar strictures with an average stricture length of 1.63 cm (SD 0.76). Significant improvements in IPSS, average Qmax and PVR were maintained at 2 years. Freedom from repeat intervention was significantly higher in the Optilume DCB arm at 2 years versus the Control arm at 1 year (77.8% vs. 23.6%, p < 0.001). During the follow-up period, there were 15 treatment failures and two non-study-related deaths. Treatment-related AEs were rare and generally self-limited (haematuria, dysuria and urinary tract infection).

Conclusion

The Optilume DCB shows sustained improvement in both objective and subjective voiding parameters at 2-year follow-up. Optilume appears to provide a safe and effective endoscopic treatment alternative for short recurrent anterior urethral strictures among men who wish to avoid or delay formal urethroplasty.

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Optilume 药物涂层球囊治疗前尿道狭窄:ROBUST III 试验的两年结果
本研究旨在报告 ROBUST III 随机试验干预组的最新两年结果,该试验评估了 Optilume 药物涂层球囊 (DCB) 与标准内窥镜治疗复发性男性前尿道狭窄的安全性和有效性。符合条件的患者包括复发性前尿道狭窄长度≤3 cm、直径≤12Fr、国际前列腺症状评分 (IPSS) ≥11、峰值流速 (Qmax) <15 mL/s的男性。患者随机接受 Optilume DCB 治疗或标准内镜治疗。2年后测量的主要疗效终点包括不再干预、IPSS、Qmax和排尿后残余物(PVR)的变化。次要终点是国际勃起功能指数(IIEF)对性功能的影响。美国和加拿大的 22 个研究机构共招募了 127 名患者(48 人随机接受标准护理扩张术,79 人接受 DCB 扩张术)。DCB治疗组的75名患者在6个月后进入开放标签阶段。参与者之前平均接受过 3.2 次内镜干预(2-10 次不等);大多数(89.9%)患者有球部狭窄,平均狭窄长度为 1.63 厘米(标清 0.76)。患者的 IPSS、平均 Qmax 和 PVR 在 2 年后仍有显著改善。与对照组相比,Optilume DCB 治疗组在 2 年后不再重复干预的比例明显更高(77.8% 对 23.6%,P < 0.001)。在随访期间,共有 15 例治疗失败和 2 例非研究相关死亡。Optilume DCB在2年随访中显示出客观和主观排尿参数的持续改善。Optilume似乎为那些希望避免或推迟正式尿道成形术的男性提供了一种安全有效的内窥镜治疗方法,可用于治疗短小的复发性前尿道狭窄。
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