Re-resection for recurrent high-grade glioma in the setting of re-irradiation: more is not always better.

Published

Journal Article

The optimal treatment for patients with recurrent high grade glioma (HGG) remains controversial. Available therapies include surgery, re-irradiation, alternating electric fields or systemic therapy. Here we investigate whether re-resection will improve survival in patients receiving repeat radiotherapy for tumor recurrence. 231 consecutive patients with recurrent HGG treated with re-irradiation between 1994 and 2012 were analyzed. 105 patients underwent re-resection. Re-irradiation was delivered using daily fractions of 3.5 Gy to a median total dose of 35 Gy. Survival was then analyzed comparing patients with and without re-resection. Overall survival (OS) and survival from the first recurrence are reported. Univariate and cox-proportional hazard modeling was performed in a step-wise multivariate analysis using known prognostic factors. The median follow-up time from initial diagnosis was 25.7 months. The median OS from initial diagnosis of the entire group was 22.5 months. There was no significant difference in median overall survival between patients who received re-resection versus no re-resection, 23 versus 21.9 months respectively (p = 0.6). Additionally, there was no difference in median survival from the time of first recurrence 10.5 months without re-resection versus 11.1 months with re-resection (p = 0.09). After adjusting for known prognostic variables, only age remained significant. Re-irradiation is an effective salvage therapy for patients with localized, progressive high grade glioma, achieving a median survival of 10-11 months from re-irradiation. Our data reveals no significant improvement in survival with the addition of re-resection to re-irradiated patients with HGG.

Full Text

Duke Authors

Cited Authors

  • Palmer, JD; Siglin, J; Yamoah, K; Dan, T; Champ, CE; Bar-Ad, V; Werner-Wasik, M; Evans, JJ; Kim, L; Glass, J; Farrell, C; Andrews, DW; Shi, W

Published Date

  • September 2015

Published In

Volume / Issue

  • 124 / 2

Start / End Page

  • 215 - 221

PubMed ID

  • 26024653

Pubmed Central ID

  • 26024653

Electronic International Standard Serial Number (EISSN)

  • 1573-7373

Digital Object Identifier (DOI)

  • 10.1007/s11060-015-1825-y

Language

  • eng

Conference Location

  • United States