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A prospective clinical and biological database for pancreatic adenocarcinoma: the BACAP cohort

BACKGROUND: The prognosis for pancreatic cancer remains poor despite diagnostic advances and treatments with new chemotherapeutic regimens. The five year survival rate remains below 3%. Consequently, there is an urgent need for new treatments to significantly improve the prognosis. In addition, ther...

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Autores principales: Canivet, Cindy, Gourgou-Bourgade, Sophie, Napoléon, Bertrand, Palazzo, Laurent, Flori, Nicolas, Guibert, Pierre, Piessen, Guillaume, Farges-Bancel, Dominique, Seitz, Jean-François, Assenat, Eric, Vendrely, Véronique, Truant, Stéphanie, Vanbiervliet, Geoffroy, Berthelémy, Philippe, Garcia, Stéphane, Gomez-Brouchet, Anne, Buscail, Louis, Bournet, Barbara
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6191891/
https://www.ncbi.nlm.nih.gov/pubmed/30326968
http://dx.doi.org/10.1186/s12885-018-4906-4
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author Canivet, Cindy
Gourgou-Bourgade, Sophie
Napoléon, Bertrand
Palazzo, Laurent
Flori, Nicolas
Guibert, Pierre
Piessen, Guillaume
Farges-Bancel, Dominique
Seitz, Jean-François
Assenat, Eric
Vendrely, Véronique
Truant, Stéphanie
Vanbiervliet, Geoffroy
Berthelémy, Philippe
Garcia, Stéphane
Gomez-Brouchet, Anne
Buscail, Louis
Bournet, Barbara
author_facet Canivet, Cindy
Gourgou-Bourgade, Sophie
Napoléon, Bertrand
Palazzo, Laurent
Flori, Nicolas
Guibert, Pierre
Piessen, Guillaume
Farges-Bancel, Dominique
Seitz, Jean-François
Assenat, Eric
Vendrely, Véronique
Truant, Stéphanie
Vanbiervliet, Geoffroy
Berthelémy, Philippe
Garcia, Stéphane
Gomez-Brouchet, Anne
Buscail, Louis
Bournet, Barbara
author_sort Canivet, Cindy
collection PubMed
description BACKGROUND: The prognosis for pancreatic cancer remains poor despite diagnostic advances and treatments with new chemotherapeutic regimens. The five year survival rate remains below 3%. Consequently, there is an urgent need for new treatments to significantly improve the prognosis. In addition, there is a big gap in terms of the screening, early diagnosis and prevention of pancreatic cancer the incidence of which is increasing dramatically. METHODS: Design: the BACAP cohort is a prospective multicenter pancreatic cancer cohort (pancreatic ductal carcinoma) with clinical and multiple biological samples; Participating centers: 15 French academic and private hospitals; Study Population: any cytologically and/or histologically proven pancreatic carcinoma regardless of the stage (resectable, borderline, locally advanced or metastatic) or treatment (surgery, palliative chemotherapy, best supportive care). At least 1500 patients will be included. Clinical data collected include: disease presentation, epidemiological and social factors, baseline biology, radiology, endoscopic ultrasound, staging, pathology, treatments, follow-up (including biological and radiological), and survival. All these data are collected and stored through an e-observation system at a centralized data center. Biological samples and derived products (i.e. before any treatment): blood, saliva, endoscopic ultrasound-guided fine needle aspiration materials from the primary tumor, fine needle biopsy of metastases and surgically resected tissue. DNA and RNA are extracted from fine needle aspiration materials and are quantified and characterized for quality. Whole blood, plasma and serum are isolated from blood samples. Frozen tissues were specifically allocated to the cohort. All derived products and saliva are stored at − 80 °C. Main end-points: i) to centralize clinical data together with multiple biological samples that are harmonized in terms of sampling, the post sampling process and storage; ii) to identify new molecular markers for the diagnosis, prognosis and possibly the predictive response to pancreatic cancer surgery and or chemotherapy. DISCUSSION: The BACAP cohort is a unique prospective biological clinical database that provides the opportunity to identify correlations between the presence/expression of a broad panel of biomarkers (DNA, RNA, miRNA, proteins, etc.), epidemiological and social data, various clinical situations, various stages and the differentiation of the tumor, treatments and survival. TRIAL REGISTRATION: ClinicalTrials.gov Identifier: NCT02818829. Registration date: June 30, 2016.
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spelling pubmed-61918912018-10-23 A prospective clinical and biological database for pancreatic adenocarcinoma: the BACAP cohort Canivet, Cindy Gourgou-Bourgade, Sophie Napoléon, Bertrand Palazzo, Laurent Flori, Nicolas Guibert, Pierre Piessen, Guillaume Farges-Bancel, Dominique Seitz, Jean-François Assenat, Eric Vendrely, Véronique Truant, Stéphanie Vanbiervliet, Geoffroy Berthelémy, Philippe Garcia, Stéphane Gomez-Brouchet, Anne Buscail, Louis Bournet, Barbara BMC Cancer Study Protocol BACKGROUND: The prognosis for pancreatic cancer remains poor despite diagnostic advances and treatments with new chemotherapeutic regimens. The five year survival rate remains below 3%. Consequently, there is an urgent need for new treatments to significantly improve the prognosis. In addition, there is a big gap in terms of the screening, early diagnosis and prevention of pancreatic cancer the incidence of which is increasing dramatically. METHODS: Design: the BACAP cohort is a prospective multicenter pancreatic cancer cohort (pancreatic ductal carcinoma) with clinical and multiple biological samples; Participating centers: 15 French academic and private hospitals; Study Population: any cytologically and/or histologically proven pancreatic carcinoma regardless of the stage (resectable, borderline, locally advanced or metastatic) or treatment (surgery, palliative chemotherapy, best supportive care). At least 1500 patients will be included. Clinical data collected include: disease presentation, epidemiological and social factors, baseline biology, radiology, endoscopic ultrasound, staging, pathology, treatments, follow-up (including biological and radiological), and survival. All these data are collected and stored through an e-observation system at a centralized data center. Biological samples and derived products (i.e. before any treatment): blood, saliva, endoscopic ultrasound-guided fine needle aspiration materials from the primary tumor, fine needle biopsy of metastases and surgically resected tissue. DNA and RNA are extracted from fine needle aspiration materials and are quantified and characterized for quality. Whole blood, plasma and serum are isolated from blood samples. Frozen tissues were specifically allocated to the cohort. All derived products and saliva are stored at − 80 °C. Main end-points: i) to centralize clinical data together with multiple biological samples that are harmonized in terms of sampling, the post sampling process and storage; ii) to identify new molecular markers for the diagnosis, prognosis and possibly the predictive response to pancreatic cancer surgery and or chemotherapy. DISCUSSION: The BACAP cohort is a unique prospective biological clinical database that provides the opportunity to identify correlations between the presence/expression of a broad panel of biomarkers (DNA, RNA, miRNA, proteins, etc.), epidemiological and social data, various clinical situations, various stages and the differentiation of the tumor, treatments and survival. TRIAL REGISTRATION: ClinicalTrials.gov Identifier: NCT02818829. Registration date: June 30, 2016. BioMed Central 2018-10-16 /pmc/articles/PMC6191891/ /pubmed/30326968 http://dx.doi.org/10.1186/s12885-018-4906-4 Text en © The Author(s). 2018 Open Access This 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
Canivet, Cindy
Gourgou-Bourgade, Sophie
Napoléon, Bertrand
Palazzo, Laurent
Flori, Nicolas
Guibert, Pierre
Piessen, Guillaume
Farges-Bancel, Dominique
Seitz, Jean-François
Assenat, Eric
Vendrely, Véronique
Truant, Stéphanie
Vanbiervliet, Geoffroy
Berthelémy, Philippe
Garcia, Stéphane
Gomez-Brouchet, Anne
Buscail, Louis
Bournet, Barbara
A prospective clinical and biological database for pancreatic adenocarcinoma: the BACAP cohort
title A prospective clinical and biological database for pancreatic adenocarcinoma: the BACAP cohort
title_full A prospective clinical and biological database for pancreatic adenocarcinoma: the BACAP cohort
title_fullStr A prospective clinical and biological database for pancreatic adenocarcinoma: the BACAP cohort
title_full_unstemmed A prospective clinical and biological database for pancreatic adenocarcinoma: the BACAP cohort
title_short A prospective clinical and biological database for pancreatic adenocarcinoma: the BACAP cohort
title_sort prospective clinical and biological database for pancreatic adenocarcinoma: the bacap cohort
topic Study Protocol
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6191891/
https://www.ncbi.nlm.nih.gov/pubmed/30326968
http://dx.doi.org/10.1186/s12885-018-4906-4
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