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Published on: October 30, 2013
Adjuvant Hyperthermic Intravesical Chemotherapy in Intermediate- and High-Risk Non-muscle Invasive Bladder Cancer.
Joana C Magalhães1, Maria Sousa2, Raquel Basto3
1Medical Oncology, Instituto Português de Oncologia de Coimbra Francisco Gentil, E.P.E., Coimbra, PRT.
Hyperthermic intravesical chemotherapy with mitomycin C (HIVEC-MMC) shows promising tolerability and efficacy for non-muscle invasive bladder cancer (NMIBC). This treatment is a viable alternative for patients with intermediate- or high-risk NMIBC, especially when Bacillus Calmette-Guérin (BCG) is not suitable.
Area of Science:
- Urology
- Oncology
- Cancer Treatment
Background:
- Non-muscle invasive bladder cancer (NMIBC) is commonly treated with transurethral resection of bladder tumor (TURBT) followed by intravesical therapies like Bacillus Calmette-Guérin (BCG) or mitomycin C (MMC).
- Limitations associated with BCG have driven the search for alternative adjuvant treatments.
- Hyperthermic intravesical chemotherapy with MMC (HIVEC-MMC) has emerged as a potential alternative for NMIBC management.
Purpose of the Study:
- To evaluate the tolerability and compliance of HIVEC-MMC in patients with intermediate-risk (IR) and high-risk (HR) NMIBC.
- To assess the disease-free survival (DFS) and overall survival (OS) outcomes associated with HIVEC-MMC treatment.
- To identify predictive factors for treatment success in NMIBC patients receiving HIVEC-MMC.
Main Methods:
- A single-center retrospective analysis included 57 patients with IR- and HR-NMIBC who received HIVEC-MMC post-TURBT.
- The treatment protocol involved induction (4 weekly instillations) and maintenance (6 monthly instillations) of HIVEC-MMC.
- Statistical analyses included descriptive statistics, Kaplan-Meier survival estimation, and Cox/logistic regression for outcome assessment.
Main Results:
- Of 57 patients, 41 (71.9%) completed the HIVEC-MMC protocol; recurrence and adverse events were primary reasons for discontinuation.
- After a median follow-up of 31 months, 61.4% of patients were disease-free, with a median DFS of 42 months.
- Completion of the maintenance phase was a significant predictor of DFS (p < 0.001) and positively impacted OS when recurrence was excluded (p=0.021).
Conclusions:
- HIVEC-MMC demonstrates a secure and well-tolerated profile with promising efficacy in IR- and HR-NMIBC.
- This approach offers a feasible therapeutic option for NMIBC patients who cannot tolerate BCG or have contraindications.
- HIVEC-MMC serves as a valuable alternative, particularly during shortages of BCG.
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