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RECRUITINGOBSERVATIONAL

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

Important: This information is not medical advice. Talk to your doctor about whether a clinical trial is right for you.

About This Trial

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.

Who May Be Eligible (Plain English)

Colorectal cancer stage III Who May Qualify: - Colorectal cancer, UICC stage III - Has received curative-intent resection and is a candidate for adjuvant chemotherapy - Patient able to understand and sign written willing to sign a consent form Who Should NOT Join This Trial: - Hereditary colorectal cancer linked to familial colonic polyposis or Lynch syndrome - Inflammatory bowel disease (Crohn's disease or ulcerative colitis) - Verified distant metastases - Not treated with adjuvant chemotherapy despite indication (incomplete treatment not included) - Treated with neoadjuvant chemo-radiation therapy - No tissue sample available for the project, or tumor content in the tissue sample is \<20% - Synchronous colorectal and non-colorectal cancer diagnosed per operative (except skin cancer other than melanoma) - Other cancers (excluding colorectal cancer or skin cancer other than melanoma) within 3 years from eligibility screening - Patients who are unlikely to comply with the protocol (e.g. uncooperative attitude), inability to return for subsequent visits) and/or otherwise considered by the Investigator to be unlikely to complete the study Colorectal cancer liver metastasis Who May Qualify: - Colorectal cancer liver metastasis - Planned for curative-intent treatment - Performance status 0-1 Who Should NOT Join This Trial: - Liver cirrhosis - Extrahepatic metastases - Other cancer within the last 5 years - Intervention not performed with curative intent - No tissue available from CRLM or primary tumor Always talk to your doctor about whether this trial is right for you.

Original Eligibility Criteria

View original clinical language
Colorectal cancer stage III Inclusion Criteria: * Colorectal cancer, UICC stage III * Has received curative-intent resection and is a candidate for adjuvant chemotherapy * Patient able to understand and sign written informed consent Exclusion Criteria: * Hereditary colorectal cancer linked to familial colonic polyposis or Lynch syndrome * Inflammatory bowel disease (Crohn's disease or ulcerative colitis) * Verified distant metastases * Not treated with adjuvant chemotherapy despite indication (incomplete treatment not included) * Treated with neoadjuvant chemo-radiation therapy * No tissue sample available for the project, or tumor content in the tissue sample is \<20% * Synchronous colorectal and non-colorectal cancer diagnosed per operative (except skin cancer other than melanoma) * Other cancers (excluding colorectal cancer or skin cancer other than melanoma) within 3 years from eligibility screening * Patients who are unlikely to comply with the protocol (e.g. uncooperative attitude), inability to return for subsequent visits) and/or otherwise considered by the Investigator to be unlikely to complete the study Colorectal cancer liver metastasis Inclusion Criteria: * Colorectal cancer liver metastasis * Planned for curative-intent treatment * Performance status 0-1 Exclusion Criteria: * Liver cirrhosis * Extrahepatic metastases * Other cancer within the last 5 years * Intervention not performed with curative intent * No tissue available from CRLM or primary tumor

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, Hamburg, Germany
Universitätsklinikum Hamburg-Eppendorf
Hamburg, Hamburg, Germany
Karolinska University Hospital
Huddinge, Stockholm County, Sweden