drugset / Trial / NCT00778102

A Study of Avastin (Bevacizumab) in Combination With mFOLFOX-6 or FOLFOXIRI in Patients With Metastatic Colorectal Cancer.

NCT00778102 ↗

Phase 2 Completed 80 enrolled Hoffmann-La Roche
RandomizedParallel-groupOpen-labelTreatment

Summary

This 2 arm study will compare the resection rate of liver metastases and safety of surgery in patients with metastatic colorectal cancer and primarily unresectable liver metastases receiving treatment with Avastin in combination with 5-FU, leucovorin and oxaliplatin with irinotecan (FOLFOXIRI) or without irinotecan (mFOLFOX-6) as first line treatment. Patients will be randomized to receive Avastin (5mg/kg iv every 2 weeks) in combination with each of these two standard neoadjuvant chemotherapy regimens. The anticipated time on study treatment is until surgery, disease progression, unacceptable toxicity or patient refusal, and the target sample size is \<100 individuals.

Timeline

Start
2008-10
Primary completion
2013-10
Completion
2013-10

Outcome

Missed primary endpoint

registry p = 0.2707; Difference in Resection Rate 12.3 (95% CI -11.0 to 35.5) NCT00778102 ↗

Drugs

EvaluationDrugModalityDoseRoute
Comparator Irinotecan Small molecule 165 mg/m2 Intravenous
Comparator Leucovorin Small molecule 200 mg/m2 Intravenous
Comparator Leucovorin Small molecule 400 mg/m2 Intravenous
Subject fluorouracil Small molecule 400 mg/m2 Intravenous
Subject fluorouracil Small molecule 2400 mg/m2 Intravenous
Subject fluorouracil Small molecule 3200 mg/m2 Intravenous
Background Bevacizumab Monoclonal antibody 5 mg/kg Intravenous
Background Oxaliplatin Small molecule 85 mg/m2 Intravenous

Indications