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Salvage fractionated stereotactic re-irradiation (FSRT) for patients with recurrent high grade gliomas progressed after bevacizumab treatment.

Wenyin ShiErik S BlomainJoshua SiglinJoshua D PalmerTu DanYang WangMaria Werner-WasikJon GlassLyndon KimVoichita Bar AdDeepak BhamidipatiJames J EvansKevin JudyChristopher J FarrellDavid W Andrews
Published in: Journal of neuro-oncology (2017)
Bevacizumab failure is a major clinical problem in the management of high grade gliomas (HGG), with a median overall survival (OS) of < 4 months. This study evaluated the feasibility and efficacy of fractionated stereotactic re-irradiation (FSRT) for patients progressed after Bevacizumab treatment. Retrospective review was conducted of 36 patients treated with FSRT after progression on bevacizumab. FSRT was most commonly delivered in 3.5 Gy fractions to a total dose of 35 Gy. Survival from initial diagnosis, as well as from recurrence and re-irradiation, were utilized as study endpoints. Univariate and multivariate analysis was performed. The median time from initial bevacizumab treatment to FSRT was 8.5 months. The median plan target volume for FSRT was 27.5 cc. The median OS from FSRT was 4.8 months. FSRT treatment was well tolerated with no grade 3 or higher toxicity. Favorable outcomes were observed in patients with recurrent HGG who received salvage FSRT after bevacizumab failure. The treatment was well tolerated. Prospective study is warranted to further evaluate the efficacy of salvage FSRT for selected patients with recurrent HGG amenable to FSRT, who had failed bevacizumab treatment.
Keyphrases
  • high grade
  • small cell lung cancer
  • metabolic syndrome
  • chronic kidney disease
  • low grade
  • newly diagnosed
  • adipose tissue
  • ejection fraction
  • metastatic colorectal cancer
  • brain metastases