drugset / Trial / NCT01023633

OPTIMOX1 in Chinese mCRC Patients

NCT01023633

Phase 4 Unknown 300 enrolled Nanjing Medical University
RandomizedParallel-groupOpen-labelTreatment

Summary

Previous OPTIMOX1 study investigated the use of oxaliplatin discontinuation and reintroduction in a novel stop-and-go strategy. Previously untreated patients were randomly assigned to either FOLFOX4 administered every 2 weeks until progression (arm A) or FOLFOX7 for 6 cycles, maintenance without oxaliplatin for 12 cycles, and reintroduction of FOLFOX7 for another 6 cycles (arm B). Data showed that there was no significant difference in median progression-free survival (PFS) and overall survival (OS) between two arms. Furthermore, this study showed lower Grade 3 neurotoxicity rate in arm B (17.9% vs 13.3%, P = 0.12).In order to investigate the efficacy and feasibility of the novel "Stop and go" strategy in Chinese mCRC patients, Prof. Shu Yongqian in JiangShu Province Hospital plans to conduct a randomized controlled study to compare continuous FOLFOX4 vs. FOLFOX4 in a Stop-and-Go Fashion in 1st Line mCRC patients. To avoid the high oxaliplatin dosage related neurotoxicity, FOLFOX4 regimen is chosen in this study.

Timeline

Start
2009-10
Primary completion
2014-01
Completion
2015-07

Drugs

EvaluationDrugModalityDoseRoute
Subject Leucovorin Small molecule 200 mg/m2
Subject Oxaliplatin Small molecule 85 mg/m2
Subject fluorouracil Small molecule 400 mg Intravenous
Subject fluorouracil Small molecule 600 mg/m2 Intravenous

Indications