Plain-English translation of NCT07114627 on ClinicalTrials.gov ↗ · Source last updated · Translation generated · How we translate trials
This research study is investigating how capecitabine, a commonly used tablet for treating breast, colon, stomach, and esophageal cancers, affects different people based on their genes. Specifically, researchers want to understand whether people who have a genetic variation in an enzyme called CES1 experience more side effects—particularly a painful condition called hand-foot syndrome—when taking this medication. By studying blood levels of the active cancer-fighting ingredient in the medication, the study aims to help doctors eventually personalize treatment and reduce these side effects.
Hand-foot syndrome is a common and painful side effect for some patients taking this medication, and researchers have noticed that people with certain genetic variations in the CES1 enzyme seem to experience it more often. This study exists to confirm that connection and understand the biological reason behind it, so doctors can eventually develop better strategies to prevent or manage these side effects.
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As a participant, you would continue receiving your standard cancer treatment with capecitabine and oxaliplatin (possibly combined with other medications) exactly as your doctor planned. The research part involves having your blood drawn at specific times so researchers can measure how much of the active cancer-fighting ingredient is in your bloodstream and monitor for side effects. You would be grouped based on your genetic CES1 type—either a variation or the standard version—so researchers can compare how the medication affects people with different genes.
AI-generated summary from trial data · Jun 4, 2026 · Not medical advice
Netherlands