RECRUITINGOBSERVATIONAL
Minimal Residual Disease Assessment in Patients With Colorectal Cancer, the MiRDA-C Study
Minimal Residual Disease Assessment in Colorectal Cancer (MiRDA-C)
About This Trial
This study investigates if circulating tumor DNA (ctDNA) and other tumor-related molecules/chemicals released in the blood can help doctors predict if colorectal cancer may come back or spread. Tumors shed DNA and other cancer related chemicals into the blood that can be identified and studied further to provide information about the cancer. Information gathered from this study may help researchers better understand if ctDNA found in the blood can predict whether colorectal cancer may come back or spread.
Who May Be Eligible (Plain English)
Who May Qualify:
1. Age ≥ 18 years.
2. Histological/cytological confirmation of colorectal adenocarcinoma.
3. Patients with any stage colorectal adenocarcinoma deemed potentially eligible for curative intent treatment. Patients with stages II-IV colorectal cancer post-R0 resection may also be enrolled onto the protocol any time before or up to 3 months post-surgery and prior to initiating adjuvant therapy.
4. Ability to understand and the willingness to sign a written willing to sign a consent form document.
5. Willing to pursue standard of care surveillance post completion of curative therapies.
6. Willing to provide blood samples for correlative research.
Who Should NOT Join This Trial:
1. Known active malignancies other than colorectal adenocarcinoma that may interfere with detection and / or interpretation of circulating plasma markers. Patients with known clonal hematopoiesis of indeterminate potential are eligible.
2. Co-morbid systemic illnesses or other severe concurrent disease which, in the judgment of the investigator, would make the patient inappropriate for entry into this study.
Always talk to your doctor about whether this trial is right for you.
Original Eligibility Criteria
View original clinical language
Inclusion Criteria:
1. Age ≥ 18 years.
2. Histological/cytological confirmation of colorectal adenocarcinoma.
3. Patients with any stage colorectal adenocarcinoma deemed potentially eligible for curative intent treatment. Patients with stages II-IV colorectal cancer post-R0 resection may also be enrolled onto the protocol any time before or up to 3 months post-surgery and prior to initiating adjuvant therapy.
4. Ability to understand and the willingness to sign a written informed consent document.
5. Willing to pursue standard of care surveillance post completion of curative therapies.
6. Willing to provide blood samples for correlative research.
Exclusion Criteria:
1. Known active malignancies other than colorectal adenocarcinoma that may interfere with detection and / or interpretation of circulating plasma markers. Patients with known clonal hematopoiesis of indeterminate potential are eligible.
2. Co-morbid systemic illnesses or other severe concurrent disease which, in the judgment of the investigator, would make the patient inappropriate for entry into this study.
Treatments Being Tested
PROCEDURE
Biospecimen Collection
Undergo collection of blood and tissue samples
OTHER
Electronic Health Record Review
Review of medical records
Locations (10)
Banner - MD Anderson Cancer Center
Gilbert, Arizona, United States
Baptist- MD Anderson Cancer Center
Jacksonville, Florida, United States
The Queen's Medical Center
Honolulu, Hawaii, United States
St. Luke's Cancer Institute
Boise, Idaho, United States
Cooper Hospital UNIV MED CTR.
Camden, New Jersey, United States
UT Southwestern/Simmons Cancer Center-Dallas
Dallas, Texas, United States
Houston Methodist Cancer Center
Houston, Texas, United States
M D Anderson Cancer Center
Houston, Texas, United States
UT Health San Antonio MD Anderson Cancer Center
San Antonio, Texas, United States
Baylor Scott & White Research Institute
Temple, Texas, United States