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原发性高级别膀胱肿瘤:进展风险的确定。

Primary Ta high grade bladder tumors: Determination of the risk of progression.

机构信息

Department of Urology, Comprehensive Cancer Center, Medical University of Vienna, Vienna, Austria; Department of Urology, King Fahad Specialist Hospital, Dammam, Saudi Arabia.

Department of Urology, Comprehensive Cancer Center, Medical University of Vienna, Vienna, Austria.

出版信息

Urol Oncol. 2021 Feb;39(2):132.e7-132.e11. doi: 10.1016/j.urolonc.2020.07.017. Epub 2020 Aug 7.

Abstract

PURPOSE

TaG3 bladder cancer is an under-investigated disease and because of its rarity it is commonly studies together with T1G3 disease. We sought to exclusively study TaG3 disease and to determine the factors associated with disease progression.

MATERIAL AND METHOD

We retrospectively studied patients with primary TaG3 bladder cancer. Progression to ≥pT1 and pT2 were analyzed using Cox and competing-risk regression analyses.

RESULTS

Of 3,505 consecutive patients with nonmuscle invasive bladder cancer, 285 patients had primary TaG3 without concomitant carcinoma in-situ. Progression to ≥pT1 occurred in 21 patients (7.4%). In a multivariable competing-risk regression analysis, intravesical Bacillus Calmette-Guerin (BCG) was significantly associated with a lower risk of progression to ≥pT1 (HR 0.23, 95%CI 0.08-0.64, P = 0.005). Recurrence in the first year of diagnosis was significantly associated with an increased risk of stage progression to ≥pT1 (HR 7.81, 95%CI 2.50-24.44, P < 0.001). Progression to ≥T2 was observed in 9 patients (3.2%). In univariable competing-risk regression analyses, intravesical BCG was significantly associated with a lower risk of progression to ≥pT2 (HR 0.11, 95%CI 0.04-0.47, P = 0.003). On the other hand, recurrence in the first year of diagnosis was significantly associated with an increased risk of stage progression to ≥T2 (HR 7.12, 95%CI 1.50-33.77, P = 0.013). In a subgroup of 199 patients who were treated with BCG, there was no statistically significant association between tumor recurrence in the 1 year of diagnosis and stage progression to ≥pT1 (P = 0.14) or ≥pT2(P = 0.19).

CONCLUSION

Patients with TaG3 bladder cancer are considered high risk but if appropriately treated with BCG that risk is considerably mitigated. Our data support that TaG3 without concomitant carcinoma in-situ should not be considered as aggressive as T1G3 as it has a lower risk of progression to muscle-invasive bladder cancer. Recurrence in the first year after diagnosis is the strongest predictor of progression to muscle-invasive bladder cancer.

摘要

目的

TaG3 膀胱癌是一种研究不足的疾病,由于其罕见性,通常与 T1G3 疾病一起研究。我们旨在专门研究 TaG3 疾病,并确定与疾病进展相关的因素。

材料和方法

我们回顾性研究了原发性 TaG3 膀胱癌患者。使用 Cox 和竞争风险回归分析来分析进展为≥pT1 和 pT2 的情况。

结果

在 3505 例非肌肉浸润性膀胱癌连续患者中,有 285 例患者患有原发性 TaG3 且无同时性原位癌。21 例患者(7.4%)进展为≥pT1。在多变量竞争风险回归分析中,膀胱内卡介苗(BCG)显著降低了进展为≥pT1 的风险(HR 0.23,95%CI 0.08-0.64,P=0.005)。诊断后第一年的复发与进展为≥pT1 的风险增加显著相关(HR 7.81,95%CI 2.50-24.44,P<0.001)。9 例患者(3.2%)进展为≥T2。在单变量竞争风险回归分析中,膀胱内 BCG 显著降低了进展为≥pT2 的风险(HR 0.11,95%CI 0.04-0.47,P=0.003)。另一方面,诊断后第一年的复发与进展为≥T2 的风险增加显著相关(HR 7.12,95%CI 1.50-33.77,P=0.013)。在 199 例接受 BCG 治疗的患者亚组中,诊断后 1 年内肿瘤复发与进展为≥pT1(P=0.14)或≥pT2(P=0.19)之间无统计学显著关联。

结论

患有 TaG3 膀胱癌的患者被认为是高风险的,但如果接受适当的 BCG 治疗,风险会大大降低。我们的数据支持这样一种观点,即没有同时性原位癌的 TaG3 不应被视为与 T1G3 一样具有侵袭性,因为它进展为肌肉浸润性膀胱癌的风险较低。诊断后第一年的复发是进展为肌肉浸润性膀胱癌的最强预测因子。

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