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A prospective multicenter study on bladder cancer: the COBLAnCE cohort

BACKGROUND: Bladder cancer is a very heterogeneous disease as regards natural history. Environmental exposures, constitutional genetic and/or epigenetic background may affect not only the likelihood of bladder tumor occurrence, but also the histologic type of cancer and its outcome. Currently, only...

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Autores principales: Benhamou, Simone, Bonastre, Julia, Groussard, Karine, Radvanyi, François, Allory, Yves, Lebret, Thierry
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5094141/
https://www.ncbi.nlm.nih.gov/pubmed/27809812
http://dx.doi.org/10.1186/s12885-016-2877-x
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author Benhamou, Simone
Bonastre, Julia
Groussard, Karine
Radvanyi, François
Allory, Yves
Lebret, Thierry
author_facet Benhamou, Simone
Bonastre, Julia
Groussard, Karine
Radvanyi, François
Allory, Yves
Lebret, Thierry
author_sort Benhamou, Simone
collection PubMed
description BACKGROUND: Bladder cancer is a very heterogeneous disease as regards natural history. Environmental exposures, constitutional genetic and/or epigenetic background may affect not only the likelihood of bladder tumor occurrence, but also the histologic type of cancer and its outcome. Currently, only a few data are available to study the prognostic role of genetic and environmental factors. Likewise, data on the economic burden of bladder cancer and the longitudinal impact of the disease and the treatments on patient quality of life are scarce. METHODS: COBLAnCE is a large French-based clinical cohort study on bladder cancer. Newly diagnosed patients are enrolled prospectively in 12 public hospitals and 5 private for profits hospitals. The target sample size is 2,000 patients. All patients are to be followed for 6 years. Information on patient characteristics and lifestyle is collected during a face-to-face interview at enrollment. Clinical information on disease presentation, diagnosis, and treatment is extracted from medical records for the primary tumor and for all subsequent local and distant recurrences. Quality of life and resource use is collected at recruitment and during follow-up. In parallel, 4 types of biological samples (blood, tumor tissue, urine and nail) are collected, at baseline and during follow-up. DNA, RNA and PBMLs are extracted from blood samples, DNA and RNA from stabilized urine, proteins from frozen urine, DNA, RNA and proteins from frozen tumor tissues, and DNA and RNA from formalin-fixed paraffin-embedded tumor tissues. All derived products are stored at −80 °C or in liquid nitrogen. Main endpoints are gene-environment interactions, molecular classification, biomarker discovery, therapeutic innovation, treatment patterns, healthcare resource use, bladder cancer outcomes and quality of life. DISCUSSION: The COBLAnCE cohort will provide considerable insight into the biology of bladder cancer and the mechanisms through which genetic and environmental factors may influence the prognosis. It may allow the discovery of emerging biomarkers. Finally, economic data will be useful for future cost-effectiveness studies of immunotherapy drugs or other therapeutics in bladder cancer.
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spelling pubmed-50941412016-11-07 A prospective multicenter study on bladder cancer: the COBLAnCE cohort Benhamou, Simone Bonastre, Julia Groussard, Karine Radvanyi, François Allory, Yves Lebret, Thierry BMC Cancer Study Protocol BACKGROUND: Bladder cancer is a very heterogeneous disease as regards natural history. Environmental exposures, constitutional genetic and/or epigenetic background may affect not only the likelihood of bladder tumor occurrence, but also the histologic type of cancer and its outcome. Currently, only a few data are available to study the prognostic role of genetic and environmental factors. Likewise, data on the economic burden of bladder cancer and the longitudinal impact of the disease and the treatments on patient quality of life are scarce. METHODS: COBLAnCE is a large French-based clinical cohort study on bladder cancer. Newly diagnosed patients are enrolled prospectively in 12 public hospitals and 5 private for profits hospitals. The target sample size is 2,000 patients. All patients are to be followed for 6 years. Information on patient characteristics and lifestyle is collected during a face-to-face interview at enrollment. Clinical information on disease presentation, diagnosis, and treatment is extracted from medical records for the primary tumor and for all subsequent local and distant recurrences. Quality of life and resource use is collected at recruitment and during follow-up. In parallel, 4 types of biological samples (blood, tumor tissue, urine and nail) are collected, at baseline and during follow-up. DNA, RNA and PBMLs are extracted from blood samples, DNA and RNA from stabilized urine, proteins from frozen urine, DNA, RNA and proteins from frozen tumor tissues, and DNA and RNA from formalin-fixed paraffin-embedded tumor tissues. All derived products are stored at −80 °C or in liquid nitrogen. Main endpoints are gene-environment interactions, molecular classification, biomarker discovery, therapeutic innovation, treatment patterns, healthcare resource use, bladder cancer outcomes and quality of life. DISCUSSION: The COBLAnCE cohort will provide considerable insight into the biology of bladder cancer and the mechanisms through which genetic and environmental factors may influence the prognosis. It may allow the discovery of emerging biomarkers. Finally, economic data will be useful for future cost-effectiveness studies of immunotherapy drugs or other therapeutics in bladder cancer. BioMed Central 2016-11-03 /pmc/articles/PMC5094141/ /pubmed/27809812 http://dx.doi.org/10.1186/s12885-016-2877-x Text en © The Author(s). 2016 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
Benhamou, Simone
Bonastre, Julia
Groussard, Karine
Radvanyi, François
Allory, Yves
Lebret, Thierry
A prospective multicenter study on bladder cancer: the COBLAnCE cohort
title A prospective multicenter study on bladder cancer: the COBLAnCE cohort
title_full A prospective multicenter study on bladder cancer: the COBLAnCE cohort
title_fullStr A prospective multicenter study on bladder cancer: the COBLAnCE cohort
title_full_unstemmed A prospective multicenter study on bladder cancer: the COBLAnCE cohort
title_short A prospective multicenter study on bladder cancer: the COBLAnCE cohort
title_sort prospective multicenter study on bladder cancer: the coblance cohort
topic Study Protocol
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5094141/
https://www.ncbi.nlm.nih.gov/pubmed/27809812
http://dx.doi.org/10.1186/s12885-016-2877-x
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