FOLFIRINOX or Gemcitabine as Adjuvant Therapy for Pancreatic Cancer
- Creators
- Conroy, Thierry
- Hammel, Pascal
- Hebbar, Mohamed
- Ben Abdelghani, Meher
- Wei, Alice
- Raoul, Jean-Luc
- Choné, Laurence
- Francois, Eric
- Artru, Pascal
- Biagi, James
- Lecomte, Thierry
- Assenat, Eric
- Faroux, Roger
- Ychou, Marc
- Volet, Julien
- Sauvanet, Alain
- Breysacher, Gilles
- Di Fiore, Frédéric
- Cripps, Christine
- Kavan, Petr
- Texereau, Patrick
- Bouhier-Leporrier, Karine
- Khemissa-Akouz, Faiza
- Legoux, Jean-Louis
- Juzyna, Beata
- Gourgou, Sophie
- O'Callaghan, Christopher
- Jouffroy-Zeller, Claire
- Rat, Patrick
- Malka, David
- Castan, Florence
- Bachet, Jean-Baptiste
- Trials Group, Canadian Cancer
- Group, Unicancer-Gi–prodige
- Others:
- Institut de Cancérologie de Lorraine - Alexis Vautrin [Nancy] (UNICANCER/ICL) ; UNICANCER
- Hôpital Beaujon ; Assistance publique - Hôpitaux de Paris (AP-HP) (AP-HP)-Université Paris Diderot - Paris 7 (UPD7)-Hôpital Beaujon [AP-HP] ; Assistance publique - Hôpitaux de Paris (AP-HP) (AP-HP)
- Hôpital Claude Huriez [Lille] ; CHU Lille
- CRLCC Paul Strauss
- Institut Paoli-Calmettes ; Fédération nationale des Centres de lutte contre le Cancer (FNCLCC)
- Service d'Hépato-gastro-entérologie [CHRU Nancy] ; Centre Hospitalier Régional Universitaire de Nancy (CHRU Nancy)
- Centre de Lutte contre le Cancer Antoine Lacassagne [Nice] (UNICANCER/CAL) ; UNICANCER-Université Côte d'Azur (UCA)
- Hôpital privé Jean Mermoz
- CHU Trousseau [Tours] ; Centre Hospitalier Régional Universitaire de Tours (CHRU Tours)
- Centre Hospitalier Régional Universitaire [Montpellier] (CHRU Montpellier)
- Institut de Génétique Moléculaire de Montpellier (IGMM) ; Université de Montpellier (UM)-Centre National de la Recherche Scientifique (CNRS)
- Centre Hospitalier Départemental - Hôpital de La Roche-sur-Yon (CHD Vendée)
- Institut de Recherche en Cancérologie de Montpellier (IRCM - U1194 Inserm - UM) ; CRLCC Val d'Aurelle - Paul Lamarque-Institut National de la Santé et de la Recherche Médicale (INSERM)-Université de Montpellier (UM)
- Centre Hospitalier Universitaire de Reims (CHU Reims)
- Service de chirurgie hepato-pancreato-biliaire ; Assistance publique - Hôpitaux de Paris (AP-HP) (AP-HP)-Université Paris Diderot - Paris 7 (UPD7)-Hôpital Beaujon [AP-HP] ; Assistance publique - Hôpitaux de Paris (AP-HP) (AP-HP)
- Hôpital Louis Pasteur [Colmar] (CH Colmar)
- CHU Rouen ; Normandie Université (NU)
- CHU Mont de Marsan
- Hôpital Côte de Nacre [CHU Caen] ; CHU Caen ; Normandie Université (NU)-Tumorothèque de Caen Basse-Normandie (TCBN)-Normandie Université (NU)-Tumorothèque de Caen Basse-Normandie (TCBN)
- Centre Hospitalier Saint Jean de Perpignan
- Centre Hospitalier Régional d'Orléans (CHRO)
- R&D UNICANCER ; Fédération Nationale des Centres de Lutte Contre le Cancer (FNCLCL/UNICANCER) ; UNICANCER-UNICANCER
- Centre Hospitalier Universitaire de Dijon - Hôpital François Mitterrand (CHU Dijon)
- Oncologie digestive ; Département de médecine oncologique [Gustave Roussy] ; Institut Gustave Roussy (IGR)-Institut Gustave Roussy (IGR)
- Service d'Hépato-Gastro-Entérologie [CHU Pitié-Salpêtrière] ; CHU Pitié-Salpêtrière [AP-HP] ; Assistance publique - Hôpitaux de Paris (AP-HP) (AP-HP)-Sorbonne Université (SU)-Assistance publique - Hôpitaux de Paris (AP-HP) (AP-HP)-Sorbonne Université (SU)
Description
BACKGROUND:Among patients with metastatic pancreatic cancer, combination chemotherapy with fluorouracil, leucovorin, irinotecan, and oxaliplatin (FOLFIRINOX) leads to longer overall survival than gemcitabine therapy. We compared the efficacy and safety of a modified FOLFIRINOX regimen with gemcitabine as adjuvant therapy in patients with resected pancreatic cancer.METHODS:We randomly assigned 493 patients with resected pancreatic ductal adenocarcinoma to receive a modified FOLFIRINOX regimen (oxaliplatin [85 mg per square meter of body-surface area], irinotecan [180 mg per square meter, reduced to 150 mg per square meter after a protocol-specified safety analysis], leucovorin [400 mg per square meter], and fluorouracil [2400 mg per square meter] every 2 weeks) or gemcitabine (1000 mg per square meter on days 1, 8, and 15 every 4 weeks) for 24 weeks. The primary end point was disease-free survival. Secondary end points included overall survival and safety.RESULTS:At a median follow-up of 33.6 months, the median disease-free survival was 21.6 months in the modified-FOLFIRINOX group and 12.8 months in the gemcitabine group (stratified hazard ratio for cancer-related event, second cancer, or death, 0.58; 95% confidence interval [CI], 0.46 to 0.73; P<0.001). The disease-free survival rate at 3 years was 39.7% in the modified-FOLFIRINOX group and 21.4% in the gemcitabine group. The median overall survival was 54.4 months in the modified-FOLFIRINOX group and 35.0 months in the gemcitabine group (stratified hazard ratio for death, 0.64; 95% CI, 0.48 to 0.86; P=0.003). The overall survival rate at 3 years was 63.4% in the modified-FOLFIRINOX group and 48.6% in the gemcitabine group. Adverse events of grade 3 or 4 occurred in 75.9% of the patients in the modified-FOLFIRINOX group and in 52.9% of those in the gemcitabine group. One patient in the gemcitabine group died from toxic effects (interstitial pneumonitis).CONCLUSIONS:Adjuvant therapy with a modified FOLFIRINOX regimen led to significantly longer survival than gemcitabine among patients with resected pancreatic cancer, at the expense of a higher incidence of toxic effects. (Funded by R&D Unicancer and others; ClinicalTrials.gov number, NCT01526135 ; EudraCT number, 2011-002026-52 .).
Abstract
International audience
Additional details
- URL
- https://hal.umontpellier.fr/hal-02281628
- URN
- urn:oai:HAL:hal-02281628v1
- Origin repository
- UNICA