Reintroduction of Oxaliplatin Is Associated With Improved Survival in Advanced Colorectal Cancer

Author:

de Gramont Aimery1,Buyse Marc1,Abrahantes Jose Cortinas1,Burzykowski Tomasz1,Quinaux Emmanuel1,Cervantes Andres1,Figer Arie1,Lledo Gérard1,Flesch Michel1,Mineur Laurent1,Carola Elisabeth1,Etienne Pierre-Luc1,Rivera Fernando1,Chirivella Isabel1,Perez-Staub Nathalie1,Louvet Christophe1,André Thierry1,Tabah-Fisch Isabelle1,Tournigand Christophe1

Affiliation:

1. From the Hôpital Saint Antoine; Hôpital Tenon; Sanofi-aventis, Paris; Clinique Saint Jean, Lyon; Hôpital Devron, Dijon; Clinique Sainte Catherine, Avignon; Hôpital de Senlis, Senlis; and Clinique Radiologique Armoricaine, Saint Brieuc, France; International Drug Development Institute, Louvain-la-Neuve; Hasselt University, Hasselt, Belgium; Hospital Clínico Universitario, Valencia; Hospital Universitario Marques de Valdecilla, Santander, Spain; and Tel Aviv Sourasky Medical Centre, Tel Aviv, Israel

Abstract

Purpose In the OPTIMOX1 trial, previously untreated patients with advanced colorectal cancer were randomly assigned to two different schedules of leucovorin, fluorouracil, and oxaliplatin that were administered until progression in the control arm or in a stop-and-go fashion in the experimental arm. The randomly assigned treatment groups did not differ significantly in terms of response rate, progression-free survival, and overall survival (OS). However, the impact of oxaliplatin reintroduction on OS was potentially masked by the fact that a large number of patients did not receive the planned oxaliplatin reintroduction or received oxaliplatin after second-line therapy in both treatment groups. Patients and Methods A Cox model was fitted with all significant baseline factors plus time-dependent variables reflecting tumor progression, reintroduction of oxaliplatin, and use of second-line irinotecan. A shared frailty model was fitted with all significant baseline factors plus the number of lines of chemotherapy received by the patient and the percentage of patients with oxaliplatin reintroduction in the center. An adjusted hazard ratio (HR) was calculated for three reintroduction classes (1% to 20%, 21% to 40%, and > 40%), using centers with no reintroduction (0%) as the reference group. Results Oxaliplatin reintroduction had an independent and significant impact on OS (HR = 0.56, P = .009). The percentage of patients with oxaliplatin reintroductions also had a significant impact on OS. Centers in which more than 40% of the patients were reintroduced had an adjusted HR for OS of 0.59 compared with centers in which no patient was reintroduced. Conclusion Oxaliplatin reintroduction is associated with improved survival in patients with advanced colorectal cancer.

Publisher

American Society of Clinical Oncology (ASCO)

Subject

Cancer Research,Oncology

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