Gemcitabine and Oxaliplatin Chemotherapy or Surveillance in Resected Biliary Tract Cancer (PRODIGE 12-ACCORD 18-UNICANCER GI): A Randomized Phase III Study

Julien Edeline(Centre Eugène Marquis), M. Benabdelghani, Aurélie Bertaut(Centre Georges François Leclerc), J. Watelet(Centre Hospitalier Régional et Universitaire de Nancy), Pascal Hammel(Hôpital Beaujon), Jean‐Paul Joly(Centre Hospitalier Universitaire Amiens-Picardie), Karim Boudjéma(Centre Hospitalier Universitaire de Rennes), Lætitia Fartoux(Sorbonne Université), Karine Bouhier‐Leporrier(Centre Hospitalier Universitaire de Caen Normandie), Jean–Louis Jouve, Roger Faroux(Centre Hospitalier Départemental Vendée), Véronique Guerin‐Meyer(Institut de Cancérologie de l'Ouest), Jean‐Emmanuel Kurtz(Hôpital d'Hautepierre), Eric Assénat(Hôpital Saint Eloi), J. F. Seitz(Hôpital de la Timone), Isabelle Baumgaertner(Assistance Publique – Hôpitaux de Paris), David Tougeron(Centre Hospitalier Universitaire de Poitiers), Christelle de la Fouchardière(Centre Léon Bérard), Catherine Lombard‐Bohas, Éveline Boucher(Centre Eugène Marquis), Trevor Stanbury(UniCancer Group), Christophe Louvet(Institute Mutualiste Montsouris), David Malka(Institut Gustave Roussy), Jean-Marc Phelip(Centre Hospitalier Universitaire de Saint-Étienne)
Journal of Clinical Oncology
February 1, 2019
Cited by 521

Abstract

PURPOSE: No standard adjuvant treatment currently is recommended in localized biliary tract cancer (BTC) after surgical resection. We aimed to assess whether gemcitabine and oxaliplatin chemotherapy (GEMOX) would increase relapse-free survival (RFS) while maintaining health-related quality of life (HRQOL) in patients who undergo resection. PATIENTS AND METHODS: infused on day 2 of a 2-week cycle) for 12 cycles (experimental arm A) or surveillance (standard arm B). Primary end points were RFS and HRQOL. RESULTS: Between July 2009 and February 2014, 196 patients were included. Baseline characteristics were balanced between the two arms. After a median follow-up of 46.5 months (95% CI, 42.6 to 49.3 months), 126 RFS events and 82 deaths were recorded. There was no significant difference in RFS between the two arms (median, 30.4 months in arm A v 18.5 months in arm B; hazard ratio [HR], 0.88; 95% CI, 0.62 to 1.25; P = .48). There was no difference in time to definitive deterioration of global HRQOL (median, 31.8 months in arm A v 32.1 months in arm B; HR, 1.28; 95% CI, 0.73 to 2.26; log-rank P = .39). Overall survival was not different (median, 75.8 months in arm A v 50.8 months in arm B; HR, 1.08; 95% CI, 0.70 to 1.66; log-rank P = .74). Maximal adverse events were grade 3 in 62% (arm A) versus 18% (arm B) and grade 4 in 11% versus 3% ( P < .001). CONCLUSION: There was no benefit of adjuvant GEMOX in resected BTC despite adequate tolerance and delivery of the regimen.


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