Colorectal Cancer Clinical Trial
Official title:
DAILY: Vitamin D, Aspirin, ExercIse, Low Saturated Fat Foods StudY in Colorectal Cancer Patients With Minimal Residual Disease
To learn if lifestyle changes (such as diet and exercise) combined with daily aspirin and vitamin D can affect the likelihood of advanced colorectal cancer coming back (recurring)
Status | Recruiting |
Enrollment | 19 |
Est. completion date | April 30, 2025 |
Est. primary completion date | April 30, 2025 |
Accepts healthy volunteers | No |
Gender | All |
Age group | 18 Years and older |
Eligibility | Inclusion Criteria: - Age = 18 years at the time of study entry - ECOG 0-1 - Histologically documented high-risk stage II, stage III, or stage IV colorectal adenocarcinoma with no evidence of disease following definitive local therapy (including surgical resection or ablation) - No radiographic evidence of disease by contrast enhanced CT chest/abdomen/pelvis - Presence of detectable ctDNA mutation that matches mutations found in tumor tissue - Completion of all standard of care adjuvant therapy - Platelet count >50,000 - Ability to give informed consent - Ability to complete all questionnaires involved in study Exclusion Criteria: - Concurrent malignancy under active treatment - Known active gastrointestinal bleeding or peptic ulcer disease - Known hypersensitivity to vitamin D or aspirin - CrCl<30 mL/min within 30 days of starting the intervention - Current usage of therapeutic anticoagulation (warfarin, Eliquis, Xarelto) - Inability to safely participate in physical activity in the opinion of the treating oncologist - Pregnant or nursing women. N.B.: urine pregnancy test will be administered as part of the screening process. - Persistent hypercalcemia or conditions predisposing to hypercalcemia (i.e., hyperparathyroidism) - Known symptomatic genitourinary stones |
Country | Name | City | State |
---|---|---|---|
United States | M D Anderson Cancer Center | Houston | Texas |
Lead Sponsor | Collaborator |
---|---|
M.D. Anderson Cancer Center |
United States,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | To estimate the ctDNA clearance rate of colorectal cancer patients with minimal residual disease | through study completion, an average of 1 year |
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