Department of Urology, Northwestern University, Chicago, IL, USA.
Nat Rev Urol. 2019 Jan;16(1):23-34. doi: 10.1038/s41585-018-0105-y.
Stage T1 bladder cancers invade the lamina propria of the bladder and, despite sharing many of the genetic features of muscle-invasive bladder cancers, are classified as non-muscle-invasive or 'superficial' tumours. Yet, patients with T1 bladder cancer have an overall mortality of 33% and a cancer-specific mortality of 14% at three years after diagnosis, suggesting that these patients have a high risk of progression and, accordingly, require meticulous surgery, endoscopic surveillance and clinical decision-making. We hypothesize that the variability in the outcomes of patients with T1 bladder cancer is a result of both tumour heterogeneity and pathological staging, as well as inconsistencies in risk stratification, endoscopic resection and schedules of delivery of BCG. Owing to limitations in clinical staging, patients with T1 bladder cancer are at risk of both undertreatment with persistent use of BCG despite recurrence, and overtreatment with early cystectomy. Understanding the molecular features of T1 bladder cancers and how they respond to BCG therapy could improve biomarkers for risk stratification to align therapy with biological risk.
T1 期膀胱癌侵犯膀胱固有层,尽管与肌层浸润性膀胱癌具有许多共同的遗传特征,但仍被归类为非肌层浸润性或“浅表”肿瘤。然而,T1 期膀胱癌患者在诊断后 3 年内的总体死亡率为 33%,癌症特异性死亡率为 14%,这表明这些患者有很高的进展风险,因此需要精心的手术、内镜监测和临床决策。我们假设 T1 期膀胱癌患者的预后差异是由于肿瘤异质性和病理分期,以及风险分层、内镜切除和卡介苗接种方案的不一致性所致。由于临床分期的局限性,T1 期膀胱癌患者存在治疗不足的风险,尽管复发但仍持续使用卡介苗,以及治疗过度的风险,即早期行膀胱切除术。了解 T1 期膀胱癌的分子特征及其对卡介苗治疗的反应,可能会改善风险分层的生物标志物,使治疗与生物学风险相匹配。