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RecruitingObservational

Minimal Residual Disease Assessment in Colorectal Cancer (MiRDA-C)

NCT ID: NCT04739072Sponsor: M.D. Anderson Cancer CenterLast updated: 2026-05-29

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

Sex: AllAge: 18 Years and olderHealthy volunteers: No
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.

Study locations (10)

Banner - MD Anderson Cancer Center

Gilbert, Arizona, 85234

Terminated

Baptist- MD Anderson Cancer Center

Jacksonville, Florida, 32207

Terminated

The Queen's Medical Center

Honolulu, Hawaii, 96813

Terminated

St. Luke's Cancer Institute

Boise, Idaho, 83712

Terminated

Cooper Hospital UNIV MED CTR.

Camden, New Jersey, 08103

Terminated

UT Southwestern/Simmons Cancer Center-Dallas

Dallas, Texas, 75390

Terminated

Houston Methodist Cancer Center

Houston, Texas, 77030

Terminated

M D Anderson Cancer Center

Houston, Texas, 77030

Recruiting
Arvind Dasari · Contact
Arvind Dasari · Principal Investigator

UT Health San Antonio MD Anderson Cancer Center

San Antonio, Texas, 78229

Terminated

Baylor Scott & White Research Institute

Temple, Texas, 76508

Terminated
Minimal Residual Disease Assessment in Patients With Colorectal Cancer, the MiRDA-C Study | Cancerify