Morristown Medical Center/Atlantic Health System and Garden State Urology, Morristown, New Jersey.
NYU Langone Urology Associates, New York, New York.
J Urol. 2023 Oct;210(4):619-629. doi: 10.1097/JU.0000000000003645. Epub 2023 Aug 7.
Low-grade intermediate-risk nonmuscle-invasive bladder cancer is a chronic illness commonly treated by repetitive transurethral resection of bladder tumor. We compared the efficacy and safety of intravesical chemoablation with UGN-102 (a reverse thermal gel containing mitomycin), with or without subsequent transurethral resection of bladder tumor, to transurethral resection of bladder tumor alone in patients with low-grade intermediate-risk nonmuscle-invasive bladder cancer.
This prospective, randomized, phase 3 trial recruited patients with new or recurrent low-grade intermediate-risk nonmuscle-invasive bladder cancer to receive initial treatment with either UGN-102 once weekly for 6 weeks or transurethral resection of bladder tumor. Patients were followed quarterly by endoscopy, cytology, and for-cause biopsy. The primary end point was disease-free survival. All patients were followed for adverse events.
Trial enrollment was halted by the sponsor to pursue an alternative development strategy after 282 of a planned 632 patients were randomized to UGN-102 ± subsequent transurethral resection of bladder tumor (n=142) or transurethral resection of bladder tumor monotherapy (n=140), rendering the trial underpowered to perform hypothesis testing. Patients were predominantly male and ≥65 years of age. Tumor-free complete response 3 months after initial treatment was achieved by 92 patients (65%) who received UGN-102 and 89 patients (64%) treated by transurethral resection of bladder tumor. The estimated probability of disease-free survival 15 months after randomization was 72% for UGN-102 ± transurethral resection of bladder tumor and 50% for transurethral resection of bladder tumor (hazard ratio 0.45). The most common adverse events (incidence ≥10%) in the UGN-102 group were dysuria, micturition urgency, nocturia, and pollakiuria.
Primary, nonsurgical chemoablation with UGN-102 for the management of low-grade intermediate-risk nonmuscle-invasive bladder cancer offers a potential therapeutic alternative to immediate transurethral resection of bladder tumor monotherapy and warrants further investigation.
低级别中危非肌肉浸润性膀胱癌是一种常见的慢性病,通常通过重复经尿道膀胱肿瘤切除术进行治疗。我们比较了腔内化疗消融联合 UGN-102(一种含有丝裂霉素的反向热凝胶)与单独行经尿道膀胱肿瘤切除术治疗低级别中危非肌肉浸润性膀胱癌患者的疗效和安全性。
这项前瞻性、随机、3 期临床试验招募了新诊断或复发的低级别中危非肌肉浸润性膀胱癌患者,分别接受 UGN-102 每周 1 次、共 6 周治疗或单独行经尿道膀胱肿瘤切除术治疗。患者每 3 个月通过内镜检查、细胞学检查和因病情需要进行活检进行随访。主要终点是无病生存率。所有患者均随访不良反应。
在计划入组的 632 例患者中,282 例患者被随机分配至 UGN-102±后续行经尿道膀胱肿瘤切除术(n=142)或单独行经尿道膀胱肿瘤切除术(n=140)后,试验赞助商停止了试验入组,以寻求替代的开发策略,导致试验无法进行假设检验。患者主要为男性和≥65 岁。初始治疗 3 个月后,接受 UGN-102 治疗的 92 例(65%)和接受经尿道膀胱肿瘤切除术治疗的 89 例(64%)患者达到肿瘤完全缓解。随机分组后 15 个月时,UGN-102+经尿道膀胱肿瘤切除术组和经尿道膀胱肿瘤切除术组的无病生存率估计值分别为 72%和 50%(风险比 0.45)。UGN-102 组最常见的不良反应(发生率≥10%)为尿痛、尿急、夜尿和尿频。
对于低级别中危非肌肉浸润性膀胱癌,采用 UGN-102 进行原发性非手术化疗消融治疗为即刻行经尿道膀胱肿瘤切除术单药治疗提供了一种潜在的治疗选择,值得进一步研究。