Dose Individualization of Chemotherapy in Patients With Gastrointestinal Cancers Lacking a Specific Liver Enzyme

Recruiting now · Phase 2

Conditions studied: Digestive Cancer, Colorectal Cancer

In brief

The goal of this clinical trial is to establish guidelines for fluoropyrimidine dose reduction according to uracilemia in patients with DPD deficiency in the treatment of digestive cancers. The main question it aims to answer is: \- Which reduction dose of fluoropyrimidine is needed for patient with DPD deficiency? Participants will: * Take the treatment with the reduction of dose stated by the protocol * Visit the clinic once every 2-3 weeks for checkups and tests for collection of adverse events

Key facts

Study ID

NCT06475352

Run by

UNICANCER

People needed

400

Starts

2025-01-20

Expected to finish

2030-01-01

Last updated by the study team

2026-04-23

Who can join

Age: 18 and older. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

• Patients with pre-treatment screening based on [U] value according to INCa/HAS recommendations.
• Eastern Cooperative Oncology Group performance status (ECOG PS) ≤2
• Fluoropyrimidine-naïve patients with gastrointestinal cancer starting chemotherapy combining fluoropyrimidine (5-FU or capecitabine) and oxaliplatin whatever the context (adjuvant, neoadjuvant, palliative) including the following regimens (the most frequently prescribed in gastrointestinal cancers):
• biweekly 5-FU and oxaliplatin (FOLFOX) +/- targeted therapy (TT)
• three-weekly capecitabine and oxaliplatin (CAPOX) +/- TT
• Age ≥ 18 years
• Patients eligible for full standard fluoropyrimidine and oxaliplatin doses regardless of DPD deficiency
• Adequate bone marrow function (cell blood count (CBC)), estimated glomerular filtration rate (DFG) ≥ 50 ml/min, alkaline phosphatase (ALP) / aspartate aminotransferase (ASAT) / alanine aminotransferase (ALAT) ≤ 5 upper limit of normal (ULN), and bilirubin ≤ 50 micromol/L
• Patient must have signed and dated a written informed consent form prior to any trial specific procedures. When the patient is physically unable to give their written consent, a trusted person of their choice, independent from the investigator or the sponsor, can confirm in writing the patient's consent.
• Women of childbearing potential must have a negative serum or urine pregnancy test.
• Patients must agree to remain abstinent or use contraceptive methods with a failure rate of < 1% per year for the duration of study treatment and within 6 months after completing treatment.
• Patients must be affiliated to a Social Security System (or equivalent).
• Patient is willing and able to comply with the protocol for the duration of the trial including undergoing treatment and scheduled visits, and examinations including follow-up.

You may not qualify if…

• Patients with complete DPD deficiency based on [U] ≥150 ng/mL
• Any prior treatment including a fluoropyrimidine
• Patients with any contraindication to treatment with fluoropyrimidine or oxaliplatin regardless of DPD deficiency
• Patients not eligible for full standard dose fluoropyrimidine and oxaliplatin for clinical reasons including older age and/or comorbidity regardless of a DPD deficiency
• Patients unwilling or unable to comply with trial obligations for geographic, social, or physical reasons, or who are unable to understand the purpose and procedures of the trial
• Recent or concomitant treatment with brivudine
• Pregnant or breastfeeding woman.
• Participation in another therapeutic trial within 30 days prior to inclusion.
• Persons deprived of their liberty or under protective custody or guardianship.

Where it is running

• Gustave Roussy Cancer Campus — Villejuif, France (enrolling)
• Hopital Henri Mondor — Aurillac, France (enrolling)
• Institut du Cancer Avignon Provence — Avignon, France (enrolling)
• CH Aunay Bayeux — Bayeux, France (enrolling)
• CH Cote Basque — Bayonne, France (enrolling)
• CHU Besançon — Besançon, France (enrolling)
• Centre François Baclesse — Caen, France (enrolling)
• Polyclinique du Parc - Centre d'Oncologie Maurice Tubiana — Caen, France (enrolling)
• CH de Saint Malo — St-Malo, France (enrolling)
• Institut du Cancer de Strasbourg — Strasbourg, France (enrolling)
• CHU de Toulouse — Toulouse, France (enrolling)
• Hopital Bretonneau — Tours, France (enrolling)
• CHU Amiens — Amiens, France (enrolling)
• Hopital Beaujon — Clichy, France (enrolling)
• Hopital Henri Mondor — Créteil, France (enrolling)
• CHU Dijon — Dijon, France (enrolling)
• GH Mutualiste de Grenoble — Grenoble, France (enrolling)
• Hopital Privé Drome-Ardeche — Guilherand-Granges, France (enrolling)
• Centre Oscar Lambret — Lille, France (enrolling)
• CHU Dupuytren — Limoges, France (enrolling)
• Hopital Privé Jean Mermoz — Lyon, France (enrolling)
• Centre Léon Bérard — Lyon, France (enrolling)
• Grand Hopital de l'Est Francilien — Meaux, France (enrolling)
• Hopital Nord Franche Comté - Site du Mittan — Montbéliard, France (enrolling)
• Centre Antoine Lacassagne — Nice, France (enrolling)

Full record on ClinicalTrials.gov

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