drugset / Trial / NCT00528567

BEATRICE Study: A Study of Bevacizumab (Avastin) Adjuvant Therapy in Triple Negative Breast Cancer

NCT00528567 ↗

Phase 3 Completed 2591 enrolled Hoffmann-La Roche
RandomizedParallel-groupOpen-labelTreatment

Summary

The main objective of the trial is to compare Invasive Disease-Free Survival (IDFS) of patients randomised to treatment with adjuvant chemotherapy alone or to adjuvant chemotherapy with 1 year of bevacizumab. The secondary objectives of this trial are to: * compare Overall Survival (OS), Breast Cancer-Free Interval (BCFI), Disease- Free Survival (DFS) and Distant Disease-Free Survival (DDFS) of patients randomised to treatment with adjuvant chemotherapy alone or to adjuvant chemotherapy in combination with 1 year of bevacizumab * evaluate the safety and tolerability of bevacizumab An exploratory sub-study (not reported here) was to identify biomarkers (from tumour or serum) predictive of toxicity and for the level of benefit from the addition of bevacizumab to standard adjuvant systemic treatment.

Timeline

Start
2007-12
Primary completion
2012-02
Completion
2014-06

Outcome

Missed primary endpoint

registry Bevacizumab and Chemotherapy vs Chemotherapy; p = 0.1810; Hazard Ratio (HR) 0.87 (95% CI 0.72 to 1.07); Log Rank NCT00528567 ↗

registry Bevacizumab and Chemotherapy vs Chemotherapy; p = 0.1966; Hazard Ratio (HR) 0.87 (95% CI 0.71 to 1.07); Log Rank NCT00528567 ↗

Drugs

EvaluationDrugModalityDoseRoute
Subject Bevacizumab Monoclonal antibody 5 mg/kg —

Indications