TY - JOUR
T1 - T1 bladder cancer
T2 - current considerations for diagnosis and management
AU - Jordan, Brian
AU - Meeks, Joshua J.
N1 - Funding Information:
J.J.M. is a consultant for Merck, AstraZeneca and Ferring, and receives research funding from Abbvie, Tesaro, NextCure and Epizyme. B.J. declares no competing interests.
Funding Information:
The authors would like to acknowledge M. K. Keeter for helpful discussions of the manuscript. J.J.M. is supported by a VA Merit Award (BX003692-01) and a SEED Award from the Hope Foundation.
Publisher Copyright:
© 2018, Springer Nature Limited.
PY - 2019/1/1
Y1 - 2019/1/1
N2 - 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.
AB - 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.
UR - http://www.scopus.com/inward/record.url?scp=85054921121&partnerID=8YFLogxK
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U2 - 10.1038/s41585-018-0105-y
DO - 10.1038/s41585-018-0105-y
M3 - Review article
C2 - 30323201
AN - SCOPUS:85054921121
SN - 1759-4812
VL - 16
SP - 23
EP - 34
JO - Nature Reviews Urology
JF - Nature Reviews Urology
IS - 1
ER -