RecruitingPhase 2NCT06475352

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

Dihydropyrimidine Dehydrogenase (DPD) Phenotype-guided Dose Individualization of Fluoropyrimidine-based Chemotherapy in DPD Deficient Patients With Gastrointestinal Cancers


Sponsor

UNICANCER

Enrollment

400 participants

Start Date

Jan 20, 2025

Study Type

INTERVENTIONAL

Conditions

Summary

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


Eligibility

Min Age: 18 Years

Inclusion Criteria13

  • 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.

Exclusion Criteria9

  • 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.

Interventions

DRUGFOLFOX regimen

Oxaliplatin will be administered at a fixed dose of 85 mg/m² by 2h intravenous (IV) infusion concurrently with folinic acid 400 mg/m² (or 200 mg/m² if L-folinic acid) as a 2 h IV infusion on day 1 of each 14-day cycle followed by 5-fluorouracil (5-FU) 400 mg/m² IV bolus on day 1, then continuous IV infusion of 1,200 mg/m² /day × 2 days (total 2400 mg/m² for 46-48 hours)

DRUGCAPOX regimen

Oxaliplatin will be administered at a fixed dose of 130 mg/m² by 2h IV infusion on day 1 of each 21-day cycle followed by capecitabine (1000 mg/m²) twice a day (BID) during 2 weeks, every 3 weeks


Locations(34)

CHU Amiens

Amiens, France

Institut du Cancer Avignon Provence

Avignon, France

CH Aunay Bayeux

Bayeux, France

CH Cote Basque

Bayonne, France

CHU Besançon

Besançon, France

Centre François Baclesse

Caen, France

Polyclinique du Parc - Centre d'Oncologie Maurice Tubiana

Caen, France

CHU Clermont Ferrand

Clermont-Ferrand, France

Hopital Beaujon

Clichy, France

Hopital Henri Mondor

Créteil, France

CHU Dijon

Dijon, France

GH Mutualiste de Grenoble

Grenoble, France

Hopital Privé Drome-Ardeche

Guilherand-Granges, France

CHU Dupuytren

Limoges, France

Hopital Privé Jean Mermoz

Lyon, France

Centre Léon Bérard

Lyon, France

Grand Hopital de l'Est Francilien

Meaux, France

Hopital Nord Franche Comté - Site du Mittan

Montbéliard, France

Centre Antoine Lacassagne

Nice, France

CHU d'Orléans

Orléans, France

Institut Curie

Paris, France

Hopital Saint Louis

Paris, France

Hopital Saint Antoine

Paris, France

GH Diaconesses Croix St Simon

Paris, France

CHU Bordeaux

Pessac, France

Hospices Civiles de Lyon

Pierre-Bénite, France

CHU Poitiers

Poitiers, France

Hopital Robert Debré

Reims, France

Institut Jean Godinot

Reims, France

CH de Saint Malo

St-Malo, France

Institut du Cancer de Strasbourg

Strasbourg, France

CHU de Toulouse

Toulouse, France

Hopital Bretonneau

Tours, France

Gustave Roussy Cancer Campus

Villejuif, France

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NCT06475352


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