Dreyer Thomas, Brandt Simone, Fabrin Knud, Azawi Nessn, Vásquez Juan Luis, Ernst Andreas, Dyrskjøt Lars, Jensen Jørgen Bjerggaard
Department of Urology, Aarhus University Hospital, Aarhus, Denmark; Department of Clinical Medicine, Aarhus University, Aarhus, Denmark.
Department of Urology, Aarhus University Hospital, Aarhus, Denmark; Department of Clinical Medicine, Aarhus University, Aarhus, Denmark.
Eur Urol. 2025 Jul;88(1):23-30. doi: 10.1016/j.eururo.2025.03.018. Epub 2025 Apr 25.
Urinary biomarker tests have long been suggested as a noninvasive alternative to current cystoscopy-based follow-up of high-grade non-muscle-invasive bladder cancer (NMIBC) to reduce both morbidity and costs. However, the clinical impact of urinary biomarker tests remains uncertain owing to a lack of randomized trials.
In this randomized noninferiority trial, we evaluated the impact of alternating a urinary biomarker test (Xpert Bladder Cancer Monitor, XBCM) with cystoscopy in the intervention arm as a method for reducing the number of cystoscopies during follow-up of patients with high-grade NMIBC. Patients in the control arm underwent cystoscopy at all follow-up visits. The primary outcome was comparison of the risk of recurrence-free survival in terms of high-grade NMIBC, muscle-invasive bladder cancer, or metastatic urothelial carcinoma between the study arms.
In total, 43 high-grade recurrences were detected, 22 in the intervention arm and 21 in the control arm. The risk difference for high-grade recurrence between the study arms was 0.08% (95% confidence interval -7.2% to 7.4%). Two pTa high-grade recurrences were missed by the XBCM test. The number of cystoscopies performed was 1029 cystoscopies in the control arm and 445 in the intervention arm. An anticipatory positive effect was observed, with XBCM positivity observed before recurrences were visible on cystoscopy. The findings are limited by a lower-than-expected rate of recurrence in both study arms.
Alternating cystoscopy with XBCM reduced the number of follow-up cystoscopies for high-grade NMIBC without affecting detection of any recurrence. The long-term oncological safety of this strategy needs to be validated over longer follow-up.
长期以来,尿生物标志物检测一直被视为一种非侵入性方法,可替代当前基于膀胱镜检查的高级别非肌层浸润性膀胱癌(NMIBC)随访,以降低发病率和成本。然而,由于缺乏随机试验,尿生物标志物检测的临床影响仍不确定。
在这项随机非劣效性试验中,我们评估了在干预组中交替使用尿生物标志物检测(Xpert膀胱癌监测仪,XBCM)和膀胱镜检查,作为减少高级别NMIBC患者随访期间膀胱镜检查次数的一种方法。对照组患者在所有随访时均接受膀胱镜检查。主要结局是比较研究组之间高级别NMIBC、肌层浸润性膀胱癌或转移性尿路上皮癌的无复发生存风险。
总共检测到43例高级别复发,干预组22例,对照组21例。研究组之间高级别复发的风险差异为0.08%(95%置信区间为-7.2%至7.4%)。XBCM检测漏诊了2例pTa高级别复发。对照组进行了1029次膀胱镜检查,干预组进行了445次。观察到一种预期的阳性效应,即在膀胱镜检查可见复发之前就观察到XBCM呈阳性。研究结果受到两个研究组复发率低于预期的限制。
膀胱镜检查与XBCM交替使用可减少高级别NMIBC的随访膀胱镜检查次数,且不影响任何复发的检测。该策略的长期肿瘤学安全性需要通过更长时间的随访来验证。