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Long-term cancer-specific outcomes of TaG1 urothelial carcinoma of the bladder

机译:TaG1膀胱尿路上皮癌的长期癌症特异性结局

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Background Few studies have investigated the natural history of TaG1 urothelial carcinoma of the bladder (UCB). Objective To assess the long-term outcomes of patients with TaG1 UCB and the impact of immediate postoperative instillation of chemotherapy (IPIC). Design, setting, and participants A retrospective analysis of 1447 patients with TaG1 UCB treated between 1996 and 2007 at eight centers. Median follow-up was 67.2 mo (interquartile range: 67.9). Patients were stratified into three European Association of Urology (EAU) guidelines risk categories; high-risk patients (n = 11) were excluded. Intervention Transurethral resection of the bladder with or without IPIC. Outcome measurements and statistical analysis Univariable and multivariable Cox regression models addressed factors associated with disease recurrence, disease progression, death of disease, and any-cause death. Results and limitations Of the 1436 patients, 601 (41.9%) and 835 (58.1%) were assigned to low- and intermediate-risk categories, respectively. The actuarial estimate of 5-yr recurrence-free survival was 56% (standard error: ±1). Advancing age (p = 0.04), tumor >3 cm (p = 0.001), multiple tumors (p < 0.001), and recurrent tumors (p < 0.001) were independently associated with increased risk of disease recurrence, whereas IPIC was associated with decreased risk (p = 0.001). The actuarial estimate of 5-yr progression-free survival was 95% ± 1. Advancing age (p < 0.001) and multiple tumors (p = 0.01) were independent risk factors for disease progression. Five-year cancer-specific survival was 98% ± 1. Advancing age (p = 0.001) and previous recurrence (p = 0.04) were associated with increased risk, whereas female gender (p = 0.02) was associated with decreased risk of cancer-specific mortality. Compared with low-risk patients, intermediate-risk patients were at significantly higher risk of disease recurrence, disease progression, and cancer-specific mortality (all p < 0.01). Limitations include the retrospective design of the study and the lack of a central pathology review. Conclusions TaG1 UCB patients experience heterogeneous risks of disease recurrence. We validated the EAU guidelines risk stratification in TaG1 UCB patients. IPIC was associated with a reduced risk of disease recurrence in patients with low- and intermediate-risk TaG1 UCB.
机译:背景技术很少有研究调查TaG1膀胱尿路上皮癌(UCB)的自然史。目的评估TaG1 UCB患者的长期预后以及术后立即滴注化疗(IPIC)的影响。设计,设置和参与者回顾性分析了1996年至2007年在八个中心治疗的1447例TaG1 UCB患者。中位随访时间为67.2 mo(四分位间距:67.9)。将患者分为三个欧洲泌尿外科协会(EAU)指南风险类别。高危患者(n = 11)被排除在外。介入性IPIC或不IPIC膀胱经尿道切除术。结果测量和统计分析单变量和多变量Cox回归模型处理与疾病复发,疾病进展,疾病死亡和任何原因死亡相关的因素。结果与局限性在1436例患者中,分别将601(41.9%)和835(58.1%)分为低危和中危类别。 5年无复发生存期的精算估计为56%(标准误:±1)。年龄增长(p = 0.04),肿瘤> 3 cm(p = 0.001),多发性肿瘤(p <0.001)和复发性肿瘤(p <0.001)与疾病复发风险增加独立相关,而IPIC与疾病复发风险增加相关风险(p = 0.001)。 5年无进展生存的精算估计为95%±1。年龄增长(p <0.001)和多个肿瘤(p = 0.01)是疾病进展的独立危险因素。五年癌症特异性生存率为98%±1。年龄增长(p = 0.001)和先前复发(p = 0.04)与增加的风险相关,而女性(p = 0.02)与降低癌症的风险相关-比死亡率。与低危患者相比,中危患者的疾病复发,疾病进展和癌症特异性死亡的风险显着更高(所有p <0.01)。局限性包括研究的回顾性设计和缺乏中央病理学检查。结论TaG1 UCB患者经历了疾病复发的不同风险。我们验证了TaG1 UCB患者的EAU指南风险分层。 IPIC与TaG1 UCB中低风险患者的疾病复发风险降低相关。

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