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Schnell, Oliver; Thorsteinsdottir, Jun; Fleischmann, Daniel Felix; Lenski, Markus; Abenhardt, Wolfgang; Giese, Armin; Tonn, Jörg-Christian; Belka, Claus; Kreth, Friedrich Wilhelm; Niyazi, Maximilian (2016): Re-irradiation strategies in combination with bevacizumab for recurrent malignant glioma. In: Journal of Neuro-Oncology, Vol. 130, No. 3: pp. 591-599
Full text not available from 'Open Access LMU'.

Abstract

The place of bevacizumab (BEV) in salvage re-irradiation (Re-RT) settings of malignant glioma is poorly defined. In the current study risk/benefit profiles of two BEV-based Re-RT protocols were analyzed and compared with that of salvage BEV plus irinotecan (BEV/IRI). According to interdisciplinary tumor board recommendations, patients were assigned to one of three BEV-based treatment protocols: (1) BEV/IRI, (2) Re-RT (36 Gy/18 fx) with concomitant BEV (Re-RT/BEV), and (3) Re-RT with concomitant/maintenance BEV (Re-RT/BEV -> BEV). Prognostic factors were obtained from proportional hazards models. Adverse events were classified according to the NCI CTCAE, v4.0. 105 consecutive patients were enrolled from 08/2008 to 05/2014. Patients undergoing Re-RT experienced longer time intervals from initial diagnosis to BEV treatment (median: 22.0 months vs. 13.7 months, p = 0.001);those assigned to Re-RT/BEV -> BEV rated better on the performance scale (median KPSREC: 90 vs. 70, p = 0.013). Post-recurrence survival after BEV-based treatment (PRS) was longest after Re-RT/BEV -> BEV (median: 13.1 months vs. 8 months, p = 0.006). PRS after Re-RT/BEV and BEV/IRI was similar. Multivariately, higher KPSREC and Re-RT/BEV -> BEV were associated with longer PRS. Treatment toxicity did not differ among groups. Re-RT/BEV -> BEV is safe, feasible and effective and deserves further prospective evaluation.