Minimal Residual Disease Assessment in Colorectal Cancer (MiRDA-C)
Summary
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.
Detailed description
PRIMARY OBJECTIVES: I. Demonstrate ability to monitor cancer-specific deoxyribonucleic acid (DNA), ribonucleic acid (RNA), and proteomic alterations from plasma. II. Improve detection of recurrences post completion of curative therapies through monitoring of plasma cancer-specific DNA, RNA and proteomic alterations. SECONDARY OBJECTIVES: I. Qualitative and quantitative changes in cancer-specific plasma alterations during neoadjuvant, adjuvant therapies and surveillance. II. Disease free survival (DFS) of patients with detectable cancer-specific plasma alterations. III. Overall survival (OS) of patients with detectable cancer-specific plasma alterations. EXPLORATORY OBJECTIVES: I. Optimal combination of cancer-specific plasma DNA, RNA and / or proteomic alterations for early detection of recurrences. II. Sensitivity, specificity, positive predictive and negative predictive values of cancer-specific plasma alterations in detecting recurrences. III. Correlation between cancer-specific alterations in plasma and tissue and either with outcomes including DFS \& OS. IV. Nature and frequency of detection of incidental non-colorectal cancer related DNA, RNA and / or proteomic alterations. OUTLINE: Patients undergo collection of blood samples at baseline, during each neoadjuvant therapy treatment, prior to surgical resection, and up to 4 times per year for up to 5 years. Patients also undergo collection of tissue sample at time of surgical resection. Patients' medical records may also be reviewed.
Arms & interventions
- ProcedureBiospecimen Collection
Undergo collection of blood and tissue samples
- OtherElectronic Health Record Review
Review of medical records
Outcome measures
Primary
Analysis of deoxyribonucleic (DNA), ribonucleic acid (RNA), and proteomic alterations from plasma
To detect circulating tumor DNA (ctDNA) in plasma samples from patients with colorectal cancer (CRC) who have completed curative therapies (i.e. minimal residual disease) towards predicting recurrence earlier than the current standard of care utilizing the CRC23 assay and the LUNAR assay from Guardant Health technology.
Time frame: Up to 5 years
Detection of recurrences post completion of curative therapies
To detect ctDNA in plasma samples from patients with CRC who have completed curative therapies (i.e. minimal residual disease) towards predicting recurrence earlier than the current standard of care utilizing the CRC23 assay and the LUNAR assay from Guardant Health technology.
Time frame: Up to 5 years
Secondary
Changes in cancer-specific plasma alterations during neoadjuvant, adjuvant therapies and surveillance
Time frame: Baseline up to 5 years
Disease free survival (DFS)
Time frame: Up to 5 years
Overall survival (OS)
Time frame: Up to 5 years
Eligibility criteria
Study locations (10)
Banner - MD Anderson Cancer Center
Gilbert, Arizona, 85234
Baptist- MD Anderson Cancer Center
Jacksonville, Florida, 32207
The Queen's Medical Center
Honolulu, Hawaii, 96813
St. Luke's Cancer Institute
Boise, Idaho, 83712
Cooper Hospital UNIV MED CTR.
Camden, New Jersey, 08103
UT Southwestern/Simmons Cancer Center-Dallas
Dallas, Texas, 75390
Houston Methodist Cancer Center
Houston, Texas, 77030
M D Anderson Cancer Center
Houston, Texas, 77030
UT Health San Antonio MD Anderson Cancer Center
San Antonio, Texas, 78229
Baylor Scott & White Research Institute
Temple, Texas, 76508