A phase II trial of single-agent bevacizumab in patients with recurrent anaplastic glioma Article

Kreisl, TN, Zhang, W, Odia, Y et al. (2011). A phase II trial of single-agent bevacizumab in patients with recurrent anaplastic glioma . NEURO-ONCOLOGY, 13(10), 1143-1150. 10.1093/neuonc/nor091

cited authors

  • Kreisl, TN; Zhang, W; Odia, Y; Shih, JH; Butman, JA; Hammoud, D; Iwamoto, FM; Sul, J; Fine, HA

authors

abstract

  • The purpose of this study was to evaluate the activity of single-agent bevacizumab in patients with recurrent anaplastic glioma and assess correlative advanced imaging parameters. Patients with recurrent anaplastic glioma were treated with bevacizumab 10 mg/kg every 2 weeks. Complete patient evaluations were repeated every 4 weeks. Correlative dynamic contrast-enhanced MR and 18fluorodeoxyglucose PET imaging studies were obtained to evaluate physiologic changes in tumor and tumor vasculature at time points including baseline, 96 h after the first dose, and after the first 4 weeks of therapy. Median overall survival was 12 months (95% confidence interval [CI]: 6.08-22.8). Median progression-free survival was 2.93 months (95% CI: 2.01-4.93), and 6-month progression-free survival was 20.9% (95% CI: 10.3%-42.5%). Thirteen (43%) patients achieved a partial response. The most common grade ≥3 treatment-related toxicities were hypertension, hypophosphatemia, and thromboembolism. Singleagent bevacizumab produces significant radiographic response in patients with recurrent anaplastic glioma but did not meet the 6-month progression-free survival endpoint. Early change in enhancing tumor volume at 4 days after start of therapy was the most significant prognostic factor for overall and progression-free survival. © The Author(s) 2011.

publication date

  • October 1, 2011

published in

Digital Object Identifier (DOI)

start page

  • 1143

end page

  • 1150

volume

  • 13

issue

  • 10