# Survival Outcomes of BCG Only, BCG Plus EMDA-MMC or Upfront Radical Cystectomy in High-Risk Non-Muscle Invasive Bladder Cancers (NMIBCs): A Multicentre, International, Collaborative Study from Tertiary Referral Institutions

**Authors:** Francesco Del Giudice, Valerio Santarelli, Amir Khan, Mohamed Gad, Katarina Spurna, Syed Ghazi Ali Kirmani, Noor Huda Bhatti, Rajesh Nair, Kathryn Chatterton, Suzanne Amery, Elsie Mensah, Benjamin Challacombe, Youssef Ibrahim, Felice Crocetto, Giuseppe Basile, Roberta Corvino, Eleonora Razeto, Matilde Verde, Vincenzo Asero, Ettore De Berardinis, Giulio Garaffa, Jan Łaszkiewicz, Aleksander Ślusarczyk, Francesco Claps, Benjamin I. Chung, Ramesh Thuraraja, Timothy O’Brien, Muhammad Shamim Khan, Yasmin Abu-Ghanem

PMC · DOI: 10.3390/cancers18030500 · 2026-02-03

## TL;DR

This study compared three treatments for high-risk bladder cancer and found that patient and tumor factors, not treatment type, most affect survival.

## Contribution

The study provides a large multicentre comparison of adjuvant therapies for high-risk non-muscle-invasive bladder cancer.

## Key findings

- No significant differences in survival outcomes were found between BCG, BCG/EMDA-MMC, and upfront radical cystectomy.
- Patient- and tumor-related factors like CIS and T stage had a greater impact on clinical outcomes.
- A second resection improved progression-free survival but treatment modality did not affect survival endpoints.

## Abstract

In patients with high- and very high-risk Non-muscle-invasive Bladder Cancer, the risk of recurrence and progression remains high despite standard therapies. This multicentre study compared three adjuvant treatment strategies: BCG, BCG combined with electromotive administration of mitomycin C, and upfront radical cystectomy. The results showed no significant differences in survival outcomes among the treatment approaches. Instead, patient- and tumour-related factors, such as tumour stage, presence of concomitant carcinoma in situ, and repeat transurethral resection, had a greater impact on clinical outcomes. These findings suggest that treatment decisions should be individualized based on disease characteristics and patients’ preferences balanced with oncologic risk and clinical judgement.

Introduction: Conservative or upfront radical management for high- and very high-risk non-muscle-invasive bladder cancer continues to be debated, particularly for cases with adverse pathological features. We aimed to compare survival outcomes among NMIBC patients treated with transurethral resection of bladder tumour (TURBT) followed by either Bacillus Calmette–Guérin (BCG), sequential BCG plus electromotive administration of mitomycin C (EMDA-MMC), or upfront radical cystectomy (RC). Materials and Methods: High- and- very high-risk NMIBC cases undergoing TURBT followed by BCG, BCG plus EMDA-MMC, or RC at two international tertiary referral centres between 2009 and 2024 were retrospectively reviewed. Recurrence-free survival (RFS), progression-free survival (PFS), and overall survival (OS) were estimated using Kaplan–Meier methods. Multivariable Cox regression models were applied to identify factors independently associated with survival outcomes. Results: A total of 1178 patients were included: 852 received BCG, 249 received BCG/EMDA-MMC, and 77 underwent upfront RC. Kaplan–Meier analysis revealed no significant differences in RFS or PFS between the BCG and BCG/EMDA-MMC groups, nor in OS between the three treatment strategies. According to multivariable analysis, concomitant carcinoma in situ (CIS) and increasing T stage at TURBT were independently associated with poorer RFS (HR 1.39; 95% CI 1.05–1.85), PFS (HR 1.95; 95% CI 1.36–2.82), and OS (HR 2.28; 95% CI 1.60–3.25). A second resection conferred a protective effect on PFS (HR 0.72; 95% CI 0.54–0.95). Treatment modality (BCG, BCG/EMDA-MMC, or upfront RC) was not significantly associated with any survival endpoint. Conclusions: In this large multicentre series of patients with high- and very high-risk NMIBC undergoing TURBT, survival outcomes were primarily influenced by clinical–pathological characteristics rather than the adjuvant treatment of choice.

## Linked entities

- **Chemicals:** mitomycin C (PubChem CID 5746)
- **Diseases:** carcinoma in situ (MONDO:0004647)

## Full-text entities

- **Diseases:** bladder cancer (MESH:D001749), Muscle Invasive Bladder Cancers (MESH:D000093284), CIS (MESH:D002278)
- **Chemicals:** EMDA (-), MMC (MESH:D016685)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Figures

3 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12896385/full.md

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Source: https://tomesphere.com/paper/PMC12896385