College of Health and Medicine, Australian National University, Canberra, ACT, Australia and SAN Prostate Centre of Excellence, Sydney Adventist Hospital, Wahroonga, NSW, Australia.
Department of Urology, China Medical University and Hospital, Taichung, Taiwan.
Prostate Cancer Prostatic Dis. 2022 Sep;25(3):576-582. doi: 10.1038/s41391-022-00548-z. Epub 2022 May 31.
To demonstrate the safety and feasibility of the Urocross Expander System (formerly branded as XFLO Expander System), an implantable nitinol tissue expander to trea t patients with lower urinary tract symptoms (LUTS) due to benign prostatic hyperplasia (BPH).
Men of 50 years or older were eligible to participate in the international, prospective, three-arm, open-label EXPANDER-1 trial if they had a prostate volume between 30 and 80 cc, prostatic urethra length between 20 and 60/80 mm, international prostate symptom score (IPSS) > 13, peak urinary flow (Qmax) < 12 mL/s, post-void residual (PVR) urine volume < 250 mL and quality of life (QoL) score ≥ 3. Patients had pre-assigned implant indwell times (1, 6, and 12 months for Arm-1, Arm-2 and Arm-3 respectively) with follow-up through 6 months (Arm-1) and 3 years (Arm-2 and Arm-3) post-retrieval.
Outcome from treated subjects with their 6-month post-retrieval will be presented in this manuscript, as data collection from longer-term follow-up is ongoing. As of May 24, 2021, 39 and 22 men (mean age: 65), respectively, had implants successfully deployed and retrieved without any complications. No cases of implant encrustation were observed. Device- and procedure-related adverse events were predominantly mild to moderate in severity. Three SAEs were reported. Only one patient required catheterization post-implant for more than three days. Improvements in clinical parameters such as IPSS, QoL, PVR and Qmax as well as sexual function were observed.
Preliminary results demonstrate that the Urocross Expander System is a feasible and safe procedure for treating BPH/LUTS. A strong signal of efficacy justifies further evaluation of this PRostatic Urethral Expansion (PURE) procedure. Negative features of earlier generations of prostatic implants such as biocompatibility, migrations and encrustation have possibly been overcome.
展示可植入性镍钛诺组织扩张器 Urocross 扩张系统(原 XFLO 扩张系统)治疗因良性前列腺增生(BPH)导致下尿路症状(LUTS)患者的安全性和可行性。
如果患者前列腺体积在 30 至 80cc 之间、前列腺尿道长度在 20 至 60/80mm 之间、国际前列腺症状评分(IPSS)>13、最大尿流率(Qmax)<12ml/s、剩余尿量(PVR)<250ml 和生活质量(QoL)评分≥3,年龄在 50 岁或以上的男性有资格参加这项国际性、前瞻性、三臂、开放标签的 EXPANDER-1 试验。患者预先分配植入物留置时间(第 1、6 和 12 个月分别用于第 1、2 和 3 臂),通过 6 个月(第 1 臂)和 3 年(第 2 和 3 臂)的随访进行评估。
截至 2021 年 5 月 24 日,39 名和 22 名男性(平均年龄:65 岁)分别成功植入和取出,没有任何并发症。未观察到植入物结壳的情况。设备和程序相关的不良事件主要为轻度至中度。报告了 3 例严重不良事件。只有一名患者在植入后需要导尿超过三天。观察到 IPSS、QoL、PVR 和 Qmax 以及性功能等临床参数的改善。
初步结果表明,Urocross 扩张系统治疗 BPH/LUTS 是一种可行且安全的方法。该方法疗效明显, justifies further evaluation of this PRostatic Urethral Expansion (PURE) procedure. justify 在此意为“证明……是正当的”。需要进一步评估这种前列腺尿道扩张(PURE)的程序。早期前列腺植入物的一些负面特征,如生物相容性、迁移和结壳,可能已经得到克服。