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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.
Afiliação
  • Canivet C; The Department of Gastroenterology and Pancreatology, CHU - Rangueil and the University of Toulouse, 1 avenue Jean Poulhès, TSA 50032, 31059, Toulouse Cedex 9, France.
  • Gourgou-Bourgade S; The Biometrics Unit - CTD Inca, the Cancer Institute and the University of Montpellier, Montpellier, France.
  • Napoléon B; The Department of Gastroenterology, Jean Mermoz Hospital, Ramsay Générale de Santé, Lyon, France.
  • Palazzo L; The Department of Endoscopy, Trocadéro Clinic, Paris, France.
  • Flori N; The Department of Oncology, the Cancer Institute and the University of Montpellier, Montpellier, France.
  • Guibert P; The Department of Oncology, Leon Bérard Institute, Lyon, France.
  • Piessen G; Univ. Lille, Department of Digestive and Oncological Surgery, Claude Huriez University Hospital, F-59000, Lille, France.
  • Farges-Bancel D; The Department of Internal Medicine, Saint-Louis Hospital and Paris 7 Diderot University, Paris, France.
  • Seitz JF; The Department of Oncology, CHU - La Timone and the University of Marseille, Marseille, France.
  • Assenat E; The Department of Oncology, CHU - ST-Eloi and the University of Montpellier, Montpellier, France.
  • Vendrely V; The Department of Oncology and Radiotherapy, CHU - Haut-Levêque and the University of Bordeaux, Bordeaux, France.
  • Truant S; The Department of Digestive Surgery and Transplantation, the CHU and the University of Lille, Lille, France.
  • Vanbiervliet G; The Department of Gastroenterology, CHU - L'Archet and the University of Nice, Nice, France.
  • Berthelémy P; The Department of Gastroenterology, Pau Hospital, Pau, France.
  • Garcia S; The Department of Pathology, CHU - Nord and the University of Marseille, Marseille, France.
  • Gomez-Brouchet A; The Biobank, the Cancer Institute and the University of Toulouse, Toulouse, France.
  • Buscail L; The Department of Gastroenterology and Pancreatology, CHU - Rangueil and the University of Toulouse, 1 avenue Jean Poulhès, TSA 50032, 31059, Toulouse Cedex 9, France.
  • Bournet B; The Department of Gastroenterology and Pancreatology, CHU - Rangueil and the University of Toulouse, 1 avenue Jean Poulhès, TSA 50032, 31059, Toulouse Cedex 9, France. Bournet.b@chu-toulouse.fr.
BMC Cancer ; 18(1): 986, 2018 Oct 16.
Article em En | MEDLINE | ID: mdl-30326968
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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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Neoplasias Pancreáticas / Bases de Dados como Assunto / Carcinoma Ductal Pancreático Idioma: En Ano de publicação: 2018 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Neoplasias Pancreáticas / Bases de Dados como Assunto / Carcinoma Ductal Pancreático Idioma: En Ano de publicação: 2018 Tipo de documento: Article