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The first multi-cancer liquid biopsy test for detection of early-stage cancer and minimal residual disease from a blood draw

Project description

Early detection of cancer with a single blood sample

Early and equitable detection and treatment are essential for cancer patients. For many types of cancer, no early, equal-access detection methods exist, posing a growing burden on healthcare systems and society. The EU-funded DeteCTCs project aims to provide a fast-track market introduction for the CellMate® innovation, aiming to improve the standard of care for cancer patient diagnosis and treatment. Combining the advanced universal circulating cancer cell capture and recognition technology, DNA sequencing and AI-powered bioinformatics, CellMate® detects multiple types of cancer at an early stage with just one blood draw. The human and economic value of the technology has been demonstrated in studies on breast, ovarian and pancreatic cancer.

Objective

With over 10M deaths and an annual cost of €199B, cancer poses an immense burden on individuals, healthcare, and society. To reduce cancer deaths, improve patients’ quality of life, and lower the economic cost, both early detection and treatment are key. Current methods for early cancer screening and minimal residual disease (MRD) testing include inconvenient and costly procedures such as mammograms, Pap smears, colonoscopies. Unfortunately, for the majority of cancers, no early detection method exists. Blood-based tests offer an attractive opportunity and receive major interest from the industry. Yet, no FDA-approved test for blood-based early cancer detection and MRD testing exists. The novel tests in development, focus on circulating tumor DNA detection. This is limited by low sensitivity, thus lacking clinical validity and utility.

The breakthrough CellMate® innovation, fast-tracked to market entry in this FTI project, will fundamentally transform the standard of care for cancer detection. Incorporating the advanced IsoPic™ universal circulating tumor cell capturing, staining technology, and AI-powered bioinformatics workflow, CellMate® detects multiple types of early-stage cancer and MRD with 90% sensitivity. Additionally, the AI-driven decision support functionality enables informed clinical decisions, including personalized treatment suggestions. Based on only a single blood draw, the molecular details of the cancer are provided in 4 days. Technology partners iCellate and QIAGEN (global leader in bioinformatic analysis) team-up with UKSH, a leading oncology institute in Europe. Together we demonstrate CellMate®’s clinical and economic value in a study with breast, ovarian, and pancreatic patients. The extensive network of our consortium ensures a broad outreach to patients, clinicians, healthcare organizations. CellMate® benefits from a multi-billion-euro (>€2.2B) market opportunity that is growing with the cancer screening market rising to ~9B by 2030.

Fields of science (EuroSciVoc)

Keywords

Programme(s)

Topic(s)

Funding Scheme

IA - Innovation action

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Call for proposal

(opens in new window) H2020-EIC-FTI-2018-2020

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Coordinator

UNIVERSITATSKLINIKUM SCHLESWIG-HOLSTEIN
Net EU contribution
€ 872 337,50
Address
Ratzeburger Allee 160
23562 Lübeck
Germany
Region
Schleswig-Holstein Schleswig-Holstein Lübeck, Kreisfreie Stadt
Activity type
Higher or Secondary Education Establishments
Links
Total cost
€ 877 337,50

Participants (3)