Re-irradiation for recurrent high-grade glioma: an analysis of prognostic factors for survival and predictors of radiation necrosis.

Abstract

Recurrent high-grade glioma (rHGG) is a heterogeneous population, and the ideal patient selection for re-irradiation (re-RT) has yet to be established. This study aims to identify prognostic factors for rHGG patients treated with re-RT. We retrospectively reviewed consecutive adults with rHGG who underwent re-RT from 2009 to 2020 from our institutional database. The primary objective was overall survival (OS). Secondary endpoints included prognostic factors for early death (< 6months after re-RT) and predictors of radiation necrosis (RN). For the 79 patients identified, the median OS after re-RT was 9.9months (95% CI 8.3-11.6). On multivariate analyses, re-resection at progression (HR 0.56, p = 0.027), interval from primary treatment to first progression ≥ 16.3months (HR 0.61, p = 0.034), interval from primary treatment to re-RT ≥ 23.9months (HR 0.35, p < 0.001), and re-RT PTV volume < 112cc (HR 0.27, p < 0.001) were prognostic for improved OS. Patients who had unmethylated-MGMT tumours (OR 12.4, p = 0.034), ≥ 3 prior systemic treatment lines (OR 29.1, p = 0.022), interval to re-RT < 23.9months (OR 9.0, p = 0.039), and re-RT PTV volume ≥ 112cc (OR 17.8, p = 0.003) were more likely to die within 6months of re-RT. The cumulative incidence of RN was 11.4% (95% CI 4.3-18.5) at 12months. Concurrent bevacizumab use (HR < 0.001, p < 0.001) and cumulative equivalent dose in 2Gy fractions (EQD2, α/β = 2) < 99 Gy2 (HR < 0.001, p < 0.001) were independent protective factors against RN. Re-RT allowed for less corticosteroid dependency. Sixty-six percent of failures after re-RTwere in-field. We observe favorable OS rates following re-RT and identified prognostic factors, including methylation status, that can assist in patient selection and clinical trial design. Concurrent use of bevacizumab mitigated the risk of RN.