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Study protocol of a phase II clinical trial of oral metformin for the intravesical treatment of non-muscle invasive bladder cancer

BACKGROUND: Non-muscle-invasive bladder cancer (NMIBC) is the most common neoplasm of the urinary tract and requires life-long invasive surveillance to detect disease recurrence. Currently, there are no effective oral therapies that delay disease recurrence or progression. We recently demonstrated t...

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Autores principales: Molenaar, Remco J., van Hattum, Jons W., Brummelhuis, Iris S., Oddens, Jorg R., Savci-Heijink, C. Dilara, Boevé, Egbert R., van der Meer, Saskia A., Witjes, J. Fred, Pollak, Michael N., de Reijke, Theo M., Wilmink, Johanna W.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6873510/
https://www.ncbi.nlm.nih.gov/pubmed/31752752
http://dx.doi.org/10.1186/s12885-019-6346-1
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author Molenaar, Remco J.
van Hattum, Jons W.
Brummelhuis, Iris S.
Oddens, Jorg R.
Savci-Heijink, C. Dilara
Boevé, Egbert R.
van der Meer, Saskia A.
Witjes, J. Fred
Pollak, Michael N.
de Reijke, Theo M.
Wilmink, Johanna W.
author_facet Molenaar, Remco J.
van Hattum, Jons W.
Brummelhuis, Iris S.
Oddens, Jorg R.
Savci-Heijink, C. Dilara
Boevé, Egbert R.
van der Meer, Saskia A.
Witjes, J. Fred
Pollak, Michael N.
de Reijke, Theo M.
Wilmink, Johanna W.
author_sort Molenaar, Remco J.
collection PubMed
description BACKGROUND: Non-muscle-invasive bladder cancer (NMIBC) is the most common neoplasm of the urinary tract and requires life-long invasive surveillance to detect disease recurrence. Currently, there are no effective oral therapies that delay disease recurrence or progression. We recently demonstrated that in mice, metformin accumulates unchanged in the urine. Urothelial cells are exposed to metformin concentrations ~ 240-fold higher than in serum. This was effective in the treatment of mouse bladder cancer models. METHODS: We describe the protocol of a multi-centre, open-label, phase II clinical trial of metformin in up to 49 evaluable patients with intermediate-risk NMIBC with the aim to determine the overall response to administration of oral metformin for 3 months on a marker tumour deliberately left following transurethral resection of multiple, papillary NMIBC tumours. All patients will receive metformin orally at doses up to 3000 mg per day. Metformin treatment will start within 2 weeks following transurethral resection of all tumours except one marker lesion. After 3 months of metformin treatment, the effect of metformin on the marker lesion is evaluated by cystoscopy and biopsy under anaesthesia. Residual tumour, if present at this evaluation, will be resected. In case of complete disappearance of the marker lesion, the former tumour area will be biopsied. The primary outcome is the complete response rate of the marker lesion, as determined by decentralised scoring of pre- and post-treatment cystoscopy images by expert independent urologists. Secondary outcomes are the partial response rate, overall safety of metformin and the duration of the time to recurrence. DISCUSSION: Preclinical studies show the potential role of oral metformin treatment in the management of NMIBC. It could offer an alternative to current adjuvant intravesical treatment. If positive, the reported results of this study could warrant further phase III trials to compare the efficacy of metformin against current treatments of intravesical installations with chemotherapy or Bacillus Calmette-Guérin (BCG). TRIAL REGISTRATION: This trial is registered in ClinicalTrials.gov under NCT03379909.
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spelling pubmed-68735102019-12-12 Study protocol of a phase II clinical trial of oral metformin for the intravesical treatment of non-muscle invasive bladder cancer Molenaar, Remco J. van Hattum, Jons W. Brummelhuis, Iris S. Oddens, Jorg R. Savci-Heijink, C. Dilara Boevé, Egbert R. van der Meer, Saskia A. Witjes, J. Fred Pollak, Michael N. de Reijke, Theo M. Wilmink, Johanna W. BMC Cancer Study Protocol BACKGROUND: Non-muscle-invasive bladder cancer (NMIBC) is the most common neoplasm of the urinary tract and requires life-long invasive surveillance to detect disease recurrence. Currently, there are no effective oral therapies that delay disease recurrence or progression. We recently demonstrated that in mice, metformin accumulates unchanged in the urine. Urothelial cells are exposed to metformin concentrations ~ 240-fold higher than in serum. This was effective in the treatment of mouse bladder cancer models. METHODS: We describe the protocol of a multi-centre, open-label, phase II clinical trial of metformin in up to 49 evaluable patients with intermediate-risk NMIBC with the aim to determine the overall response to administration of oral metformin for 3 months on a marker tumour deliberately left following transurethral resection of multiple, papillary NMIBC tumours. All patients will receive metformin orally at doses up to 3000 mg per day. Metformin treatment will start within 2 weeks following transurethral resection of all tumours except one marker lesion. After 3 months of metformin treatment, the effect of metformin on the marker lesion is evaluated by cystoscopy and biopsy under anaesthesia. Residual tumour, if present at this evaluation, will be resected. In case of complete disappearance of the marker lesion, the former tumour area will be biopsied. The primary outcome is the complete response rate of the marker lesion, as determined by decentralised scoring of pre- and post-treatment cystoscopy images by expert independent urologists. Secondary outcomes are the partial response rate, overall safety of metformin and the duration of the time to recurrence. DISCUSSION: Preclinical studies show the potential role of oral metformin treatment in the management of NMIBC. It could offer an alternative to current adjuvant intravesical treatment. If positive, the reported results of this study could warrant further phase III trials to compare the efficacy of metformin against current treatments of intravesical installations with chemotherapy or Bacillus Calmette-Guérin (BCG). TRIAL REGISTRATION: This trial is registered in ClinicalTrials.gov under NCT03379909. BioMed Central 2019-11-21 /pmc/articles/PMC6873510/ /pubmed/31752752 http://dx.doi.org/10.1186/s12885-019-6346-1 Text en © The Author(s). 2019 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Study Protocol
Molenaar, Remco J.
van Hattum, Jons W.
Brummelhuis, Iris S.
Oddens, Jorg R.
Savci-Heijink, C. Dilara
Boevé, Egbert R.
van der Meer, Saskia A.
Witjes, J. Fred
Pollak, Michael N.
de Reijke, Theo M.
Wilmink, Johanna W.
Study protocol of a phase II clinical trial of oral metformin for the intravesical treatment of non-muscle invasive bladder cancer
title Study protocol of a phase II clinical trial of oral metformin for the intravesical treatment of non-muscle invasive bladder cancer
title_full Study protocol of a phase II clinical trial of oral metformin for the intravesical treatment of non-muscle invasive bladder cancer
title_fullStr Study protocol of a phase II clinical trial of oral metformin for the intravesical treatment of non-muscle invasive bladder cancer
title_full_unstemmed Study protocol of a phase II clinical trial of oral metformin for the intravesical treatment of non-muscle invasive bladder cancer
title_short Study protocol of a phase II clinical trial of oral metformin for the intravesical treatment of non-muscle invasive bladder cancer
title_sort study protocol of a phase ii clinical trial of oral metformin for the intravesical treatment of non-muscle invasive bladder cancer
topic Study Protocol
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6873510/
https://www.ncbi.nlm.nih.gov/pubmed/31752752
http://dx.doi.org/10.1186/s12885-019-6346-1
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