drugset / Trial / NCT01989780

Bevacizumab Plus Paclitaxel Optimization Study With Interventional Aintenance Endocrine Therapy in Breast Cancer

NCT01989780 ↗

RandomizedParallel-groupOpen-labelTreatment

Summary

To compare continuing bevacizumab + paclitaxel or switching to bevacizumab + endocrine maintenance therapy followed by bevacizumab + paclitaxel, after 1st line induction therapy with bevacizumab + paclitaxel in ER+HER2- advanced or metastatic breast cancer.

Timeline

Start
2014-01
Primary completion
2018-06
Completion
2019-06

Outcome

Met primary endpoint

paper TFS was significantly longer in the endocrine therapy plus bevacizumab group than in the weekly paclitaxel plus bevacizumab group PMID 35405087 ↗

paper hazard ratio 0·51 [0·34-0·75]; p=0·0006 PMID 35405087 ↗

Drugs

EvaluationDrugModalityDoseRoute
Subject Anastrozole Other / unclassified — —
Subject Bevacizumab Monoclonal antibody 10 mg/kg Intravenous
Subject Exemestane Small molecule — —
Subject Fulvestrant Small molecule — —
Subject Goserelin Other / unclassified — —
Subject Letrozole Other / unclassified — —
Subject Leuprolide Other / unclassified — —
Subject Paclitaxel Small molecule 90 mg/m2 Intravenous

Indications