Ali Deb Abdalla, Chitteti Pragnitha, Naushad Naufal, Asaad Wael, Leung Steve, Alice Hartley, Hosam Serag
Department of Urology, James Cook University Hospital, Middlesbrough, UK.
Department of Urology, North Tees University Hospital, Stockton, UK.
Urol Res Pract. 2024 Mar 31;50(2):72-84. doi: 10.5152/tud.2024.23215.
To examine the safety and efficacy of chemoablation using UGN-101 in patients with upper tract urothelial cancer (UTUC). We conducted a systematic search through 7 databases/registries to identify key observational and experimental studies reporting either the efficacy or safety of UGN-101 in UTUC patients regardless of the risk or grade of the disease. The outcomes included efficacy (complete/partial/no response, survival, death, recurrence, or progression) and safety endpoints. All meta-analyses were conducted through STATA. The prevalence rate and its 95% CI were pooled across studies. A subgroup meta-analysis was conducted on follow-up. The quality was assessed using the Newcastle Ottawa Scale. Twenty studies (1051 patients) were analyzed. Complete response was reported in 49% (39%-60%) of cases, and 5% (0%- 15%) had disease progression. Treatment cessation was reported in 13% (3%-27%) of patients. Four percent of cases needed radical nephroureterectomy. Recurrence and death occurred in 14% (7%-23%) and 6% (2%-10%) of patients. Complications occurred in 63% (39%-85%), the majority of which were of grades I, II, and III. Ureteral stenosis was the most common complication accounting for 35% of cases. Chemoablationrelated complications occurred more than procedure-related ones. Based on available evidence, the intracavitary instillation of UGN-101 gel provides an alternative therapeutic option for upper tract urothelial cancer. Chemoablation provides good clinical outcomes in terms of complete response, disease progression and recurrence, and the need to undergo nephroureterectomy. Complications were encountered in more than half the population; however, most of them were of low grades.
研究UGN - 101化学消融术在上尿路尿路上皮癌(UTUC)患者中的安全性和有效性。我们通过7个数据库/登记处进行了系统检索,以确定报告UGN - 101在UTUC患者中的有效性或安全性的关键观察性和实验性研究,无论疾病的风险或分级如何。结局包括有效性(完全缓解/部分缓解/无反应、生存、死亡、复发或进展)和安全性终点。所有荟萃分析均通过STATA进行。汇总各研究的患病率及其95%置信区间。对随访进行亚组荟萃分析。使用纽卡斯尔渥太华量表评估质量。分析了20项研究(1051例患者)。49%(39% - 60%)的病例报告为完全缓解,5%(0% - 15%)出现疾病进展。13%(3% - 27%)的患者报告停止治疗。4%的病例需要进行根治性肾输尿管切除术。14%(7% - 23%)的患者出现复发,6%(2% - 10%)的患者死亡。63%(39% - 85%)出现并发症,其中大多数为I、II和III级。输尿管狭窄是最常见的并发症,占病例的35%。与化学消融相关的并发症比与手术相关的并发症更多。基于现有证据,UGN - 101凝胶腔内灌注为上尿路尿路上皮癌提供了一种替代治疗选择。化学消融术在完全缓解、疾病进展和复发以及进行肾输尿管切除术的必要性方面提供了良好的临床结局。超过一半的患者出现并发症;然而,大多数并发症为低级别。