RecruitingNCT06111105

GUIDE.MRD-01-CRC: Clinical Validation and Benchmarking of Top Performing CtDNA Diagnostics - Colorectal Cancer

GUIding Multi-moDal ThErapies Against MRD by Liquid Biopsies in Colorectal Cancer - GUIDE.MRD-01-CRC


Sponsor

Claus Lindbjerg Andersen

Enrollment

590 participants

Start Date

Aug 1, 2023

Study Type

OBSERVATIONAL

Conditions

Summary

Improving personalized cancer treatments and finding the best strategies to treat each patient relies on using new diagnostic technologies. Currently, for colorectal cancer, the methods used to decide who gets additional post-surgery treatment are suboptimal. Some patients get too much treatment, while others do not get enough. There is a new way to explore if there is any cancer left in a patient's body using circulating tumor DNA (ctDNA) detected in blood samples. This can help decide who needs more treatment after surgery. Even though many tests have been developed, it has yet to be determined which test performs best at relevant time points. The GUIDE.MRD consortium is a group of experts, including scientists, technology, and pharmaceutical companies. The consortium is working on creating a reliable standard for the ctDNA tests, validating their clinical utility, and collecting data to help decide on the best treatment for each patient. GUIDE.MRD-01-CRC is a part of the GUIDE.MRD project.


Eligibility

Min Age: 18 Years

Plain Language Summary

Simplified for easier understanding

This study validates and compares the best available blood tests for detecting circulating tumor DNA (ctDNA) — tiny fragments of cancer DNA shed into the bloodstream — in patients with stage III colorectal cancer or colorectal cancer that has spread to the liver. ctDNA tests may help detect cancer recurrence earlier than standard imaging. **You may be eligible if...** - You have stage III colorectal cancer and have undergone curative surgery and are a candidate for follow-up chemotherapy, OR - You have colorectal cancer that has spread to the liver and are planned for curative-intent treatment - You are able to understand and sign informed consent **You may NOT be eligible if...** - You have hereditary colorectal cancer conditions (familial polyposis or Lynch syndrome) - You have confirmed spread to distant organs (other than liver for the liver metastasis group) - You have had another cancer (other than colorectal or skin) in the last 3–5 years - Sufficient tumor tissue is not available for testing - You have liver cirrhosis (for the liver metastasis group) Talk to your doctor to see if this trial is right for you.

This summary was AI-generated to explain the trial in plain language. It is not medical advice. Always discuss eligibility with your doctor before enrolling in a clinical trial.

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Locations(15)

Abteilung für Onkologie, Medizinische Universität Graz

Graz, Styria, Austria

Ordenskrankenhaus Graz Mitte

Graz, Styria, Austria

Bispebjerg Hospital

Copenhagen, Capital Region of Denmark, Denmark

Herlev Hospital

Herlev, Capital Region of Denmark, Denmark

Aarhus University Hospital

Aarhus, Central Jutland, Denmark

Gødstrup Hospital

Herning, Central Jutland, Denmark

Regional Hospital Horsens

Horsens, Central Jutland, Denmark

Regional Hospital Randers

Randers, Central Jutland, Denmark

Regional Hospital Viborg

Viborg, Central Jutland, Denmark

Aalborg University Hospital

Aalborg, North Denmark, Denmark

Odense University Hospital

Odense, The Region of Southern Denmark, Denmark

LCCRH (Laboratoire Cellules Circulantes Rares Humaines) - CHU de Montpellier

Montpellier, France

Department of General-, Visceral- and Thoracic Surgery, University Medical Center Hamburg-Eppendorf

Hamburg, Free and Hanseatic City of Hamburg, Germany

Universitätsklinikum Hamburg-Eppendorf

Hamburg, Free and Hanseatic City of Hamburg, Germany

Karolinska University Hospital

Huddinge, Stockholm County, Sweden

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NCT06111105


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