Related Experiment Video
Updated: May 23, 2025

Induction of Invasive Transitional Cell Bladder Carcinoma in Immune Intact Human MUC1 Transgenic Mice: A Model for Immunotherapy Development
Published on: October 30, 2013
Towards Defining Follow-up Strategies for Patients with Primary Intermediate-risk Non-muscle-invasive Bladder Cancer
Roberto Contieri1, Alberto Martini2, Irene J Beijert3
1Department of Surgical Oncology (Urology), Netherlands Cancer Institute-Antoni van Leeuwenhoek Hospital, Amsterdam, The Netherlands; Department of Biochemical Science, Humanitas University, Milan, Italy; Department of Urology, Humanitas Clinical and Research Institute IRCCS, Rozzano, Italy.
Tumor size and multifocality, not grade, predict recurrence in intermediate-risk non-muscle-invasive bladder cancer (IR-NMIBC). Tailoring follow-up schedules based on individual recurrence risk improves early detection.
Area of Science:
- Urology
- Oncology
- Bladder Cancer Research
Background:
- Current European Association of Urology (EAU) guidelines categorize non-muscle-invasive bladder cancer (NMIBC) into four risk groups.
- A 2024 update introduced a specific follow-up schedule for intermediate-risk (IR) NMIBC, based on expert opinion and limited to primary low-grade or high-grade/grade 2 disease.
- There is a need to identify subgroups within IR-NMIBC requiring more intensive surveillance.
Purpose of the Study:
- To identify a subgroup of patients with intermediate-risk non-muscle-invasive bladder cancer (IR-NMIBC) who may benefit from more stringent follow-up protocols.
- To determine predictors of recurrence in IR-NMIBC.
- To refine risk stratification for IR-NMIBC patients.
Main Methods:
- Retrospective analysis of 2086 patients with IR-NMIBC using the World Health Organization 1973 grading scheme.
- Multivariable Cox-regression models to identify recurrence predictors.
- Dichotomization into low (IR-Low) and high (IR-High) recurrence risk groups based on identified predictors.
- Kaplan-Meier analysis for recurrence-free survival (RFS) and progression-free survival (PFS).
Main Results:
- Multifocality and tumor size ≥3 cm were significant predictors of higher recurrence risk, defining the IR-High group.
- The 3-year recurrence-free survival rate was significantly worse for the IR-High group (51%) compared to the IR-Low group (68%).
- The risk of progression was low in both groups (5-year PFS rate 96%), with no significant difference observed.
Conclusions:
- Tumor size and focality are more critical than grade for predicting recurrence in IR-NMIBC.
- Follow-up schedules for IR-NMIBC should be individualized based on recurrence risk.
- More stringent follow-up protocols are recommended for IR-NMIBC patients identified as higher risk for recurrence.

