Kwong Jethro C C, Pace Keiran, Al-Daqqaq Zizo, Chelliahpillai Yashan, Lee Soomin, Kim Kellie, Ringa Maximiliano, Ali Amna, Wettstein Marian, Chan Amy, Lajkosz Katherine, van der Kwast Theodorus, Perlis Nathan, Lee Jason Y, Hamilton Robert J, Fleshner Neil E, Finelli Antonio, Jamal Munir, Papanikolaou Frank, Short Thomas, Feifer Andrew, Kulkarni Girish S, Zlotta Alexandre R
Division of Urology, Department of Surgery, University of Toronto, Toronto, Ontario, Canada.
Division of Urology, Department of Surgery, University Health Network, Toronto, Ontario, Canada.
BJU Int. 2025 Aug;136(2):236-244. doi: 10.1111/bju.16793. Epub 2025 May 26.
To assess whether the distribution of concomitant carcinoma in situ (CIS; unifocal or multifocal) with papillary non-muscle-invasive bladder cancer (NMIBC) impacts the risk of progression, as concomitant CIS is an established risk factor for progression in papillary NMIBC and commonly used calculators do not make this distinction.
In this multi-institutional retrospective cohort study from both academic and community hospitals, clinicopathological data were collected from patients with pTa/pT1 NMIBC treated from 2005 to 2022. Unifocal concomitant CIS was defined as CIS present in only one specimen (i.e., papillary disease with CIS at the tumour base or isolated CIS in one specimen). Multifocal concomitant CIS was characterised by CIS in multiple specimens. Progression was defined as the development of muscle-invasive or metastatic disease. Fine-Gray regression was performed to identify progression-associated factors, using all-cause mortality as a competing risk.
Among 2923 patients, 383 (13%) progressed over a median (interquartile range) follow-up of 5.1 (3.0-8.5) years. Concomitant CIS was found in 327 patients (11%), with 233 and 94 harbouring unifocal and multifocal CIS, respectively. Recurrent tumours, T1 stage, high-grade disease, multifocal CIS, and multiple tumours were independently associated with increased progression risk (all P < 0.05). Among patients with concomitant CIS, multifocal CIS remained a significant prognosticator (sub-distribution hazard ratio 1.90, 95% confidence interval 1.18-3.05; P = 0.008) adjusting for age, sex, tumour history, stage, grade, number of tumours, tumour diameter, and Bacillus Calmette-Guérin treatment.
Papillary NMIBC progression risk varies with concomitant CIS distribution. Only multifocal concomitant CIS is a risk factor for progression in patients with T1 NMIBC. If validated in further studies, risk calculators should consider including this CIS distinction. Submitting separate specimens at the time of transurethral resection, as recommended by guidelines, should be encouraged.
评估伴有原位癌(CIS;单灶性或多灶性)的乳头状非肌层浸润性膀胱癌(NMIBC)的分布是否会影响疾病进展风险,因为伴发CIS是乳头状NMIBC进展的既定风险因素,而常用的风险计算器并未区分这一点。
在这项来自学术医院和社区医院的多机构回顾性队列研究中,收集了2005年至2022年接受治疗的pTa/pT1期NMIBC患者的临床病理数据。单灶性伴发CIS定义为仅在一个标本中存在CIS(即肿瘤基底伴有CIS的乳头状病变或一个标本中的孤立CIS)。多灶性伴发CIS的特征是多个标本中存在CIS。疾病进展定义为肌层浸润性或转移性疾病的发生。采用Fine-Gray回归分析确定与进展相关的因素,将全因死亡率作为竞争风险。
在2923例患者中,383例(13%)在中位(四分位间距)5.1(3.0 - 8.5)年的随访期内出现疾病进展。327例(11%)患者伴有CIS,其中233例和94例分别为单灶性和多灶性CIS。复发性肿瘤、T1期、高级别疾病、多灶性CIS和多发肿瘤与疾病进展风险增加独立相关(均P < 0.05)。在伴有CIS的患者中,调整年龄、性别、肿瘤病史、分期、分级、肿瘤数量、肿瘤直径和卡介苗治疗后,多灶性CIS仍然是一个显著的预后因素(亚分布风险比1.90,95%置信区间1.18 - 3.05;P = 0.008)。
乳头状NMIBC的进展风险因伴发CIS的分布而异。仅多灶性伴发CIS是T1期NMIBC患者疾病进展的风险因素。如果在进一步研究中得到验证,风险计算器应考虑纳入这种CIS的区分。应鼓励按照指南建议在经尿道切除时提交单独的标本。