Section of Urology, Department of Surgery, Dartmouth-Hitchcock Medical Center, One Medical Center Drive, Lebanon, NH, 03756, USA.
Geisel School of Medicine at Dartmouth, 1 Rope Ferry Road, Hanover, NH, 03755, USA.
J Pediatr Urol. 2019 Aug;15(4):309-314. doi: 10.1016/j.jpurol.2019.06.013. Epub 2019 Jun 22.
Urothelial cell carcinoma (UCC) of the bladder is exceedingly rare in pediatric patients. Limited data are available to guide management in this population.
The authors systematically searched MEDLINE, Cochrane Library, and Google Scholar (through February 2019) for case reports and series to summarize data regarding presentation, evaluation, management, and follow-up for patients ≤ 18 years diagnosed with UCC of the bladder. Patient-level data were abstracted, and adjusted logistic regression was used to identify factors associated with a combined outcome of recurrence or death.
One hundred two articles describing 243 patients from 26 countries met criteria. Average age was 12.5 years, 32.6% were female, 15.3% had medical comorbidities, and 13.2% had known risk factors for bladder cancer. Initial management was transurethral resection in 95.5% of patients, whereas 6.2% required secondary intervention. Tumor stage was TaN0M0 in 86.4% and low grade in 93.4%. Recurrence and death occurred in 8.6% and 3.7%, respectively. Mean time to recurrence or death was 8.6 months (standard deviation [SD] 7.6) for 10.7%. Mean disease free follow-up without recurrence or death was 56.9 months (SD 54.2) for 89.3%. Patients with comorbidities, risk factors, or family history (odds ratio [OR]: 2.4, 95% confidence interval [CI]: 1.02-5.6); ≥TaN0M0 disease (OR: 6.2, 95% CI: 2.5-15.6); and larger tumors at diagnosis (OR: 1.7, 95% CI: 1.2-2.4) had significantly greater adjusted odds of recurrence or death after initial treatment.
Based on pooled results, disease recurrence or death occurred in 10.7% of pediatric patients and within 9 months for most and within 32 months for all patients. This may suggest that low-grade and stage UCC of the bladder in pediatric patients can be systematically monitored for at least 3 years. However, prospective evaluation of this clinical strategy is warranted.
儿童膀胱尿路上皮癌极其罕见。目前针对该人群,可用的治疗方法数据有限。
作者系统地检索了 MEDLINE、Cochrane 图书馆和 Google Scholar(截至 2019 年 2 月)中的病例报告和系列研究,以总结≤18 岁诊断为膀胱尿路上皮癌患者的临床表现、评估、治疗和随访数据。提取患者水平数据,采用调整后的逻辑回归分析确定与复发或死亡复合结局相关的因素。
26 个国家的 102 篇文章描述了 243 例患者,符合纳入标准。平均年龄为 12.5 岁,32.6%为女性,15.3%存在合并症,13.2%有膀胱癌的已知危险因素。95.5%的患者初始治疗为经尿道膀胱肿瘤切除术,6.2%需要二次干预。86.4%的患者肿瘤分期为 TaN0M0,93.4%为低级别。复发和死亡的发生率分别为 8.6%和 3.7%。10.7%的患者中位复发或死亡时间为 8.6 个月(标准差[SD]为 7.6),89.3%的患者中位无疾病随访时间为 56.9 个月(SD 为 54.2)。合并症、危险因素或家族史(比值比[OR]:2.4,95%置信区间[CI]:1.02-5.6)、≥TaN0M0 疾病(OR:6.2,95%CI:2.5-15.6)和较大肿瘤(OR:1.7,95%CI:1.2-2.4)的患者初始治疗后复发或死亡的调整比值比显著更高。
基于汇总结果,10.7%的患儿出现疾病复发或死亡,大多数患者在 9 个月内出现,所有患者在 32 个月内出现。这可能表明,在儿童患者中,低级别和低分期的膀胱尿路上皮癌可以至少系统性监测 3 年。然而,需要对这一临床策略进行前瞻性评估。