RecruitingNCT07114627

Impact of CES1 Genotype on Capecitabine Exposure in Cancer Patients

Exploratory Study of Capecitabine Pharmacokinetics and Hand-foot Syndrome in CES1 Variant Carriers: the ESCAPE Study


Sponsor

Erasmus Medical Center

Enrollment

66 participants

Start Date

Feb 18, 2025

Study Type

OBSERVATIONAL

Conditions

Summary

In this study, the drug capecitabine is investigated. Capecitabine is commonly used to treat breast, colon, and stomach cancers. Capecitabine is taken in tablet form. In the body, capecitabine is converted into the active molecule that has anti-cancer effects. This molecule is called 5-FU. The transformation of capecitabine to 5-FU occurs through specific proteins in the liver, also known as enzymes. Unfortunately, capecitabine can also cause side effects. One of the most common side effects is hand-foot syndrome. In hand-foot syndrome, the palms of the hands and soles of the feet become red and painful. Previous research has shown that patients in whom one of the enzymes responsible for converting capecitabine in the liver does not function properly experience an increase in side effects frequency, particularly severe hand-foot syndrome. This specific enzyme is called CES1. It is believed that side effects occur more frequently because capecitabine is transformed more slowly, eventually leading to a prolonged exposure to 5-FU in the body. In roughly one in three people, this enzyme functions less efficiently. To gain a better understanding of how this mechanism works, we aim to conduct this study. In this study, we will examine if patients with a less effective CES1 enzyme have higher amounts of 5-FU in their blood. We will also look into whether these patients develop side effects, such as hand-foot syndrome, more frequently. This information could eventually help us develop new strategies to reduce side effects for these patients in the future.


Eligibility

Min Age: 18 Years

Plain Language Summary

Simplified for easier understanding

This study is investigating how a gene variant in an enzyme called CES1 affects how the body processes capecitabine, a common oral chemotherapy drug used to treat various cancers. Understanding this may help doctors personalize chemotherapy dosing. **You may be eligible if...** - You are 18 or older - You are about to start standard treatment with capecitabine plus oxaliplatin (for a cancer such as colorectal) - Your doctor has confirmed you are fit to receive this chemotherapy combination **You may NOT be eligible if...** - You carry certain gene variants that affect how you break down capecitabine (DPYD variants *2A, *7, *13, etc.) - You have had stomach or bowel surgery that would affect drug absorption (such as gastric bypass) - You have previously been treated with fluoropyrimidine chemotherapy - You are currently taking medications that block the enzyme DPD - You are pregnant 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

DRUGBlood sampling for pharmacokinetics

Extra blood samples are collected for assement of the pharmacokinetics of capecitabine.


Locations(1)

Erasmus MC Cancer Institute

Rotterdam, Netherlands

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NCT07114627


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