Two phase I/II clinical trials for the treatment of urinary incontinence with autologous mesenchymal stem cells

Author:

Garcia-Arranz Mariano12,Alonso-Gregorio Sergio3,Fontana-Portella Pamela4,Bravo Elena5,Diez Sebastian Jesus6,Fernandez-Santos María Eugenia7,Garcia-Olmo Damian12

Affiliation:

1. New Therapies Laboratory Health Research Institute-Fundación Jiménez Díaz University Hospital (IIS-FJD), Madrid, Spain

2. Surgery Department Autonoma University of Madrid, Madrid, Spain

3. Department of Urology Hospital De la Cruz Roja San José y Santa Adela, Madrid, Spain

4. Department of Urology La Paz University Hospital, Madrid, Spain

5. Department of Plastic Surgery La Paz University Hospital, Madrid, Spain

6. Statistics Department La Paz University Hospital, Madrid, Spain

7. GMP-Cell Production Unit Instituto de Investigación Sanitaria Gregorio Marañón (IiSGM), Madrid, Spain

Abstract

Abstract We evaluated the safety and feasibility of adipose-derived mesenchymal stem cells to treat endoscopically urinary incontinence after radical prostatectomy in men or female stress urinary. We designed two prospective, nonrandomized phase I-IIa clinical trials of urinary incontinence involving 9 men (8 treated) and 10 women to test the feasibility and safety of autologous mesenchymal stem cells for this use. Cells were obtained from liposuction containing 150 to 200 g of fat performed on every patient. After 4 to 6 weeks and under sedation, endoscopic intraurethral injection of the cells was performed. On each visit (baseline, 1, 3, 6, and 12 months), clinical parameters were measured, and blood samples, urine culture, and uroflowmetry were performed. Every patient underwent an urethrocystoscopy and urodynamic studies on the first and last visit. Data from pad test, quality-of-life and incontinence questionnaires, and pads used per day were collected at every visit. Statistical analysis was done by Wilcoxon signed-rank test. No adverse effects were observed. Three men (37.5%) and five women (50%) showed an objective improvement of >50% (P < .05) and a subjective improvement of 70% to 80% from baseline. In conclusion, intraurethral application of stem cells derived from adipose tissue is a safe and feasible procedure to treat urinary incontinence after radical prostatectomy or in female stress urinary incontinence. A statistically significant difference was obtained for pad-test improvement in 3/8 men and 5/10 women. Our results encourage studies to confirm safety and to analyze efficacy. Lessons learned • This safety clinical trial made use of mesenchymal stem cells for the treatment of urinary incontinence.• Intraurethral application of stem cells derived from adipose tissue is a safe and feasible procedure to treat urinary incontinence.  Significance statementThis article reports the results of two clinical trials that studied safety of the treatment of urinary incontinence in men and women through the use of mesenchymal stem cells derived from adipose tissue obtained from the patient or cultured ex vivo.

Funder

European Regional Development Fund

European Social Fund

Comunidad de Madrid

RETIC Program of ISCIII-FEDER

Spanish Ministry of Health and Consumer Affairs

Publisher

Oxford University Press (OUP)

Subject

Cell Biology,Developmental Biology,General Medicine

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