Service d'Urologie et Chirurgie de la Transplantation, Hospices Civils de Lyon, Lyon, France; Université Claude Bernard-Lyon 1, Lyon, France.
Service d'Urologie et Chirurgie de la Transplantation, Hospices Civils de Lyon, Lyon, France; Université Claude Bernard-Lyon 1, Lyon, France.
Eur Urol Focus. 2022 Sep;8(5):1226-1237. doi: 10.1016/j.euf.2021.06.007. Epub 2021 Jun 23.
Delay in treatment is a prognostic factor in muscle-invasive bladder cancer.
To evaluate clinical outcomes associated with delays in diagnosis and treatment for patients with non-muscle invasive bladder cancer (NMIBC).
DESIGN, SETTING, AND PARTICIPANTS: In this retrospective study we analyzed data for patients treated at our center between November 2008 and December 2016 for intermediate risk (IR) or high risk (HR) NMIBC with an additional intravesical treatment.
Time delays from diagnosis to first transurethral resection (TT-TUR), from resection to restaging resection (TT-reTUR), and from the last resection to first instillation (TT-INST) of bacillus Calmette-Guérin (BCG) or mitomycin C (MMC) were documented. To identify the interval of time from which recurrence rates significantly increased, we used nonparametric series regression. Recurrence-free survival (RFS) and progression-free survival for patients in each time delay category were compared using the Kaplan-Meier method. Factors associated with tumor recurrence were analyzed in a multivariable model.
A total of 434 patients were included, of whom 168 (38.7%) had IR and 266 (61.3%) had HR NMIBC. Among the patients, 34.6% had reTUR, 63.6% received BCG, and 36.4% received MMC. The median TT-TUR, TT-reTUR, and TT-INST was 4.0 wk, 6.5 wk, and 7.0 wk, respectively. At 40 mo the rate of recurrence was 28.4% and the rate of progression was 7.3%. Nonparametric analysis revealed that each week in delay increased the risk of recurrence, starting from week 6 for TT-TUR for IR and HR cases, and starting from week 7 for TT-INST for IR cases. RFS was significantly lower with TT-TUR > 6 wk among patients in the IR (p < 0.001) and HR (p = 0.04) groups, and with TT-INST >7 wk for patients in the IR group (p = 0.001). TT-reTUR >7 wk had a significant negative impact on progression (p < 0.017). Multivariable analysis revealed that for IR and HR cases, multifocality (p = 0.02 and p = 0.007) and TT-TUR >6 wk (p = 0.001 and p = 0.03) were independent predictors of recurrence, while TT-INST >7 wk predicted recurrence (p = 0.04) for IR NMIBC.
Our results suggest that delays of >6 wk to first TUR in IR and HR NMIBC, and >7 wk to first instillation in IR cases are associated with increases in the risk of recurrence. TT-reTUR of >7 wk is also associated with higher risk of progression.
We evaluated the impact of treatment delays on outcomes for patients with intermediate- and high-risk bladder cancer not invading the bladder wall muscle. We found that delays from diagnosis to first bladder resection, from first resection to repeat resection, and from last resection to bladder instillation treatment increase the rates of cancer recurrence and progression. The medical team should avoid delays in treatment, even for low-grade bladder cancer.
治疗延误是肌层浸润性膀胱癌的预后因素。
评估非肌层浸润性膀胱癌(NMIBC)患者诊断和治疗延误与临床结局的相关性。
设计、地点和参与者:在这项回顾性研究中,我们分析了 2008 年 11 月至 2016 年 12 月期间在我们中心接受治疗的中危(IR)或高危(HR)NMIBC 患者的数据,这些患者伴有附加的膀胱内治疗。
记录从诊断到第一次经尿道膀胱肿瘤切除术(TT-TUR)、从切除到再次切除(TT-reTUR)以及从最后一次切除到第一次卡介苗(BCG)或丝裂霉素 C(MMC)灌注的时间延迟。为了确定复发率显著增加的时间间隔,我们使用了非参数系列回归。使用 Kaplan-Meier 方法比较每个时间延迟类别的无复发生存率(RFS)和无进展生存率。在多变量模型中分析与肿瘤复发相关的因素。
共纳入 434 例患者,其中 168 例(38.7%)为 IR,266 例(61.3%)为 HR NMIBC。患者中有 34.6%接受了 reTUR,63.6%接受了 BCG 治疗,36.4%接受了 MMC 治疗。TT-TUR、TT-reTUR 和 TT-INST 的中位时间分别为 4.0 周、6.5 周和 7.0 周。在 40 个月时,复发率为 28.4%,进展率为 7.3%。非参数分析显示,从第 6 周开始,IR 和 HR 病例的 TT-TUR 每延迟一周,以及从第 7 周开始,IR 病例的 TT-INST 每延迟一周,都会增加复发的风险。IR (p < 0.001)和 HR (p = 0.04)组中 TT-TUR > 6 周与 RFS 显著降低相关,IR 组中 TT-INST > 7 周与 RFS 显著降低相关(p = 0.001)。TT-reTUR > 7 周对进展有显著的负面影响(p < 0.017)。多变量分析显示,对于 IR 和 HR 病例,多灶性(p = 0.02 和 p = 0.007)和 TT-TUR > 6 周(p = 0.001 和 p = 0.03)是复发的独立预测因素,而 TT-INST > 7 周预测了 IR NMIBC 的复发(p = 0.04)。
我们的研究结果表明,IR 和 HR NMIBC 中首次 TUR 延迟 > 6 周,以及 IR 病例中首次灌注延迟 > 7 周,与复发风险增加相关。TT-reTUR > 7 周也与更高的进展风险相关。
我们评估了治疗延迟对中危和高危膀胱癌患者的影响,这些患者的膀胱癌没有侵犯膀胱壁肌肉。我们发现,从诊断到首次膀胱切除术、从首次切除术到再次切除术、从最后一次切除术到膀胱内灌注治疗的时间延迟会增加癌症复发和进展的风险。医疗团队应避免治疗延误,即使是低度膀胱癌。