drugset / Trial / NCT02633189

Study Comparing Bevacizumab + Erlotinib vs Erlotinib Alone as First Line Treatment of Patients With EGFR Mutated Advanced Non Squamous Non Small Cell Lung Cancer

NCT02633189 ↗

Phase 3 Unknown 200 enrolled National Cancer Institute, Naples
RandomizedParallel-groupOpen-labelTreatment

Summary

The purpose of this study is to test whether the combination of bevacizumab and erlotinib can prolong progression free survival as compared with erlotinib alone as first-line treatment in patients with non small cell lung cancer (NSCLC) with activating mutation of EGFR.

Timeline

Start
2016-04
Primary completion
2023-12
Completion
2024-07

Outcome

Met primary endpoint

paper The addition of bevacizumab to first-line erlotinib prolonged PFS in Italian patients with EGFR-mutated NSCLC PMID 35659580 ↗

paper hazard ratio = 0.66, 95% CI: 0.47-0.92 PMID 35659580 ↗

paper Blinded independent centrally reviewed PFS analysis confirmed this result. PMID 35659580 ↗

Drugs

EvaluationDrugModalityDoseRoute
Subject Bevacizumab Monoclonal antibody 15 mg/kg Intravenous
Subject Erlotinib Small molecule 150 mg Oral