Department of Urology, The University of Texas MD Anderson Cancer Center, Houston, Texas.
Brady Urological Institute, The Johns Hopkins University, Baltimore, Maryland.
J Urol. 2022 Apr;207(4):779-788. doi: 10.1097/JU.0000000000002350. Epub 2021 Dec 17.
Our goal was to evaluate long-term safety and durability of response to UGN-101, a mitomycin-containing reverse thermal gel, as primary chemoablative treatment for low-grade upper tract urothelial carcinoma.
In this open-label, single-arm, multicenter, phase 3 trial (NCT02793128), patients ≥18 years of age with primary or recurrent biopsy-proven low-grade upper tract urothelial carcinoma received 6 once-weekly instillations of UGN-101 via retrograde catheter to the renal pelvis and calyces. Those with complete response (defined as negative ureteroscopic evaluation, negative cytology and negative for-cause biopsy) 4-6 weeks after the last instillation were eligible for up to 11 monthly maintenance instillations and were followed for ≥12 months with quarterly evaluation of response durability. Durability of complete response was determined by ureteroscopic evaluation; duration of response was estimated by the Kaplan-Meier method. Treatment-emergent adverse events (TEAEs) were monitored.
Of 71 patients who initiated treatment, 41 (58%) had complete response to induction therapy and consented to long-term followup; 23/41 patients (56%) remained in complete response after 12 months (95% CI 40, 72), comprising 6/12 (50%) who did not receive any maintenance instillations and 17/29 (59%) who received ≥1 maintenance instillation. Kaplan-Meier analysis of durability was estimated as 82% (95% CI 66, 91) at 12 months. Ureteric stenosis was the most frequently reported TEAE (31/71, 44%); an increasing number of instillations appeared to be associated with increased incidence of urinary TEAEs.
Durability of response to UGN-101 with or without maintenance treatment is clinically meaningful, offering a kidney-sparing therapeutic alternative for patients with low-grade disease.
我们的目的是评估 UGN-101(一种含丝裂霉素的逆向热凝胶)作为低级别上尿路上皮癌一线化学消融治疗的长期安全性和疗效持久性。
在这项开放标签、单臂、多中心、3 期临床试验(NCT02793128)中,年龄≥18 岁、经活检证实为原发性或复发性低级别上尿路上皮癌的患者接受 6 次每周一次的 UGN-101 逆行灌注,灌注部位为肾盂和肾盏。末次灌注后 4-6 周完全缓解(定义为输尿管镜检查评估阴性、细胞学检查阴性且无因活检阳性)的患者有资格接受最多 11 次每月维持灌注,并在≥12 个月时每季度评估缓解持久性。完全缓解的持久性通过输尿管镜检查评估;反应持续时间通过 Kaplan-Meier 方法估计。监测治疗后出现的不良事件(TEAEs)。
在开始治疗的 71 例患者中,有 41 例(58%)对诱导治疗有完全缓解,并同意进行长期随访;41 例中有 23 例(56%)在 12 个月后仍保持完全缓解(95%CI 40,72),其中 6 例(50%)未接受任何维持灌注,17 例(59%)接受了≥1 次维持灌注。12 个月时,Kaplan-Meier 分析的持久性估计为 82%(95%CI 66,91)。输尿管狭窄是最常报告的 TEAEs(71/71,44%);随着灌注次数的增加,尿路 TEAEs 的发生率似乎也随之增加。
接受或不接受维持治疗的 UGN-101 反应持久性具有临床意义,为低级别疾病患者提供了一种保肾的治疗选择。