Abstract

BackgroundIn case of high grade non-muscle invasive bladder cancer (HG-NMIBC), intravesical BCG represents the first-line treatment; despite the “gold” standard therapy, up to 50% of patients relapse, needing radical cystectomy. Hence, alternative therapeutic strategies have been developed. The aim of the study was to evaluate a first-line salvage treatment with EMDA®-MMC in patients with HGNMIBC unresponsive to BCG.MethodsWe carried out a prospective, single-center, single-arm Phase II study in order to evaluate the efficacy (in terms of recurrence and progression) and the safety of the EMDA®-MMC treatment in 26 (21 male, 5 female) consecutive patients with “BCG refractory” HGNMIBC on a 3 years follow-up.EMDA®-MMC treatment consisted of 40 mg of MMC diluted in 100 ml of sterile water retained in the bladder for 30 min with 20 mA pulsed electric current.EMDA®-MMC regimen consisted of an induction course of 6 weekly instillations followed by a maintenance course of 6 monthly instillations.Follow-up was performed with systematic mapping biopsies of the bladder (with sampling in the prostatic urethra for men), voiding and washing urinary cytology, radiological study of the upper urinary tract.We performed Survival Kaplan-Meier curves and Log-rank test in order to analyze high grade disease-free survival.ResultsAt the end of follow-up, 16 patients (61.5%) preserved their native bladder; 10 patients (38.4%) underwent radical cystectomy, in 6 patients (23.1%) for recurrent HGNMIBC and in 4 patients (15.4%) for progression to muscle-invasive disease.At the end of follow-up, stratifying patients based on TNM classification (TaG3, T1G3, Cis, TaT1G3 + Cis), disease-free rates were 75, 71.4, 50 and 25%, respectively; survival curves showed statistically significant differences (p value < 0.05).Regarding toxicity, we reported severe adverse systemic event of hypersensitivity to the MMC in 3 patients (11.5%), and local side effects in 6 patients (26.1%).ConclusionsIn the field of alternative strategies to radical cystectomy, the EMDA®-MMC could be considered safe and effective in high-risk NMIBC unresponsive to BCG, as a “bladder sparing” therapy in selected patients. Multicenter studies with a larger number of patients and a longer follow-up might confirm our preliminary results.Trial registrationEudraCT2017-002585-43. 17 June 2017 (retrospectively registered).

Highlights

  • In case of high grade non-muscle invasive bladder cancer (HG-NMIBC), intravesical Bacillus of Calmette Guerin (BCG) represents the first-line treatment; despite the “gold” standard therapy, up to 50% of patients relapse, needing radical cystectomy

  • Three out of 26 patients had early systemic adverse events due to ElectroMotive Drug Administration (EMDA)®-Mitomycin C (MMC) treatment leading to discontinuation of therapy; all of these 3 patients had recurrent papillary tumor at the enrollment and they had persistent high-grade disease at the endoscopic control after the discontinuation of the treatment, they underwent radical cystectomy

  • At the end of the induction course, 3 patients (11.5%) had a low-grade tumor recurrence and we considered this partial response as a success of the induction EMDA®-MMC course

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Summary

Introduction

In case of high grade non-muscle invasive bladder cancer (HG-NMIBC), intravesical BCG represents the first-line treatment; despite the “gold” standard therapy, up to 50% of patients relapse, needing radical cystectomy. Intravesical Bacillus of Calmette Guerin (BCG) represents the first-line treatment in case of high grade non muscle invasive bladder cancer (HG-NMIBC), following trans-urethral resection of bladder tumor (TURBT) [1, 2]. With the aim to preserve the bladder (new) alternative therapeutic strategies to early radical cystectomy have been developed, always taking into account the aggressiveness of HG-NMIBC [8,9,10,11,12,13,14,15]

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