drugset / Trial / NCT01390948

A Study of Bevacizumab (Avastin) in Combination With Temozolomide (TMZ) and Radiotherapy in Paediatric and Adolescent Participants With High-Grade Glioma

NCT01390948 ↗

Phase 2 Completed 124 enrolled Hoffmann-La Roche
RandomizedParallel-groupOpen-labelTreatment

Summary

This randomized, open-label, multicenter, 2-arm study will investigate the efficacy, safety, tolerability and pharmacokinetics of bevacizumab when added to postoperative radiotherapy with concomitant and adjuvant TMZ as compared to postoperative radiotherapy with concomitant and adjuvant TMZ alone in paediatric participants with newly diagnosed histologically confirmed World Health Organization (WHO) Grade III or IV localized supratentorial or infratentorial cerebellar or peduncular high grade glioma (HGG). Participants will be randomly assigned to one of two treatment arms. Upon approval by the Health Authorities/Ethics Committees in the participating countries, an additional young participant cohort (YPC) (children \>/= 6 months and \< 3 years of age with progressive or relapsed metastatic or localized, supra- or infratentorial, non-brain stem WHO Grade III or IV HGG) was included in the study. Children in the YPC will receive bevacizumab and TMZ without radiation therapy. The anticipated time on study treatment is over 1 year.

Timeline

Start
2011-10-18
Primary completion
2016-02-05
Completion
2020-01-29

Outcome

Missed primary endpoint

registry analysis (unspecified test); Chemoradiation + TMZ vs Chemoradiation + Bevacizumab + TMZ; p = 0.1292; Hazard Ratio (HR) 1.44 (95% CI 0.90 to 2.30); Log Rank NCT01390948 ↗

paper Adding BEV to RT+TMZ did not improve EFS in pediatric patients with newly diagnosed HGG. PMID 29412784 ↗

Publications

Drugs

EvaluationDrugModalityDoseRoute
Subject Bevacizumab Monoclonal antibody 10 mg/kg —
Background Temozolomide Small molecule 200 mg/m2 —

Indications