RecruitingPhase 2NCT05343013

TAS-102 With or Without Celecoxib in ctDNA-defined Minimal Residual Disease in Colorectal Cancer After Completion of Adjuvant Chemotherapy


Sponsor

M.D. Anderson Cancer Center

Enrollment

25 participants

Start Date

Jun 6, 2022

Study Type

INTERVENTIONAL

Conditions

Summary

To measure the level of circulating tumor DNA (ctDNA) in the blood of colorectal cancer patients after 6 months of receiving TAS-102 therapy. ctDNA is genetic material from tumor cells that can be found and measured in the blood.


Eligibility

Min Age: 18 Years

Plain Language Summary

Simplified for easier understanding

This study is testing whether adding celecoxib (an anti-inflammatory drug) to TAS-102 (an oral chemotherapy) can clear residual cancer signals — detected by a blood test called ctDNA — in colorectal cancer patients who finished their standard chemotherapy but still show signs of microscopic remaining disease. **You may be eligible if...** - You have been diagnosed with colorectal cancer (stage II, III, or IV) - You had successful surgery to remove all visible cancer (R0 resection) - You completed at least 3 months of oxaliplatin-based chemotherapy - A blood test (ctDNA assay) shows minimal residual disease - No cancer is visible on imaging **You may NOT be eligible if...** - You have visible cancer on imaging - You have not completed your planned curative-intent treatment - You have health conditions that prevent the use of TAS-102 or celecoxib Talk to your doctor to see if this trial is right for you.

This summary was AI-generated to explain the trial in plain language. It is not medical advice. Always discuss eligibility with your doctor before enrolling in a clinical trial.

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Interventions

DRUGTAS-102

GIven by PO


Locations(1)

MD Anderson Cancer Center

Houston, Texas, United States

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NCT05343013


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