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Active HORIZON European Commission

PANcreatic CAncer Initial Detection via liquid biopsy

€9.85M EUR

Funder European Commission
Recipient Organization Universitaetsklinikum Hamburg-Eppendorf
Country Germany
Start Date Jan 01, 2023
End Date Dec 31, 2027
Duration 1,825 days
Number of Grantees 19
Roles Participant; Associated Partner; Third Party; Coordinator
Data Source European Commission
Grant ID 101096309
Grant Description

Pancreatic cancer (PDAC) is usually detected at late stages and most patients die within one year after diagnosis. In PANCAID we will therefore develop a blood test for early detection of PDAC.

Despite tremendous technological advances in Liquid Biopsy Diagnostics (LBx), this goal is very ambitious because small tumors release only minute amounts of cells or cellular products (e.g., DNA, RNA, protein, metabolites) into the circulation.

Thus, tests with a high sensitivity are required but increases in sensitivity are usually achieved on the expenses of reduced specificity which can lead to significant overdiagnosis leading to unnecessary stress for the individuals with a false-positive blood test and high costs for the health system.

In PANCAID, we will therefore establish a blood test with high accuracy by analyzing large cohorts of patients with PDAC and its precursor lesions, individuals at risk to develop PDAC and appropriate age-matched control groups (healthy and non-cancer diseases frequent in the targeted population).

Ambitious objectives of PANCAID include (1) establishment of a unique resource of blood samples of early PDAC and risk groups (WP1); (2) Establishment of a breakthrough blood test for early diagnosis of PDAC (WP2); (3) Identification of the best composite biomarker panel by integrating multimodal features in an AI-assisted computational analysis; (4) Analysis of the socio-economic impact of early PDAC diagnosis (WP4); and (5) Definition of the ethics parameters relevant to early PDAC detection (WP5).

A robust multi-biomarker panel will be determined during the training period (year 1-3) and subsequently validated on bio-banked blood samples (year 4-5).

Depending on the outcome of this comprehensive analysis, PANCAID will provide the design of a future prospective study for validation of the developed composite blood test in an international multi-center setting required to introduce LBx into screening programs for high-risk individuals. This action is part of the Cancer Mission cluster of projects on Prevention, including Screening.

All Grantees

Fundacion Sector Publico Estatal Centro Nacional Investigaciones Oncologicas Carlos Iii; Maccabi Sheirutei Briut Foundation; The Chancellor Masters and Scholars of the University of Cambridge; Medizinische Universitat Graz; Pancreatic Cancer Europe; Universitatsklinikum Schleswig-Holstein; Uppsala Universitet; Fundacion Para la Investigacion Biomedica Del Hospital Universitario Ramon Y Cajal; Christian-Albrechts-Universitaet Zu Kiel; Collective Minds Radiology Ab; Umea Universitet; Centre Hospitalier Universitaire Montpellier; Universitaetsklinikum Hamburg-Eppendorf; Universitatsklinikum Heidelberg; Karolinska Institutet; Zava Global Gmbh; The Hebrew University of Jerusalem; Region Stockholm; Concentris Research Management Gmbh

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