drugset / Trial / NCT06813976

PRODIGE 98 : Randomized, Multicenter Phase 3 Trial of Adjuvant Chemotherapy With Modified FOLFIRINOX Versus Capecitabine or Gemcitabine in Patients With Resected Ampullary Adenocarcinoma

NCT06813976

Phase 3 Recruiting 294 enrolled Centre Hospitalier Universitaire Dijon
RandomizedParallel-groupOpen-labelTreatment

Summary

Ampullary adenocarcinoma (AMPAC) is a rare cancer (0.2% of digestive cancers) affecting the ampulla of Vater. The only curative treatment is surgery, but around 4% of patients recur within 2 years of surgical resection. The aim of adjuvant chemotherapy is to reduce the risk of disease recurrence, and the only chemotherapies that can be considered standard to date are capecitabine and gemcitabine. In this trial, an alternative experimental treatment strategy using modified FOLFORINOX (mFOLFORINOX) is proposed. It consists of 3 chemotherapies with complementary actions: 5-fluorouracil, irinotecan and oxaliplatin, combined with folic acid a vitamin that enhances the efficacy of 5-fluorouracil. This study proposes 2 treatment schemes: * Group A: mFOLFIRINOX: oxaliplatin, irinotecan, 5-fluorouracil, with folinic acid, * group B: mono-chemotherapy with capecitabine or gemcitabine.

Timeline

Start
2025-07-02
Primary completion
2033-07
Completion
2033-07

Drugs

EvaluationDrugModalityDoseRoute
Comparator Capecitabine Small molecule 1250 mg/m2
Comparator Gemcitabine Small molecule 1000 mg/m2
Subject Irinotecan Small molecule 150 mg/m2
Subject Leucovorin Small molecule 400 mg/m2
Subject Oxaliplatin Small molecule 85 mg/m2
Subject fluorouracil Small molecule 2400 mg/m2