Background Glioblastoma (GBM) is the most aggressive primary brain tumor in adults. Dexamethasone (DEX) is commonly used to manage peritumoral edema, but its impact on overall survival (OS) and progression-free survival (PFS) remains unclear across treatment phases. Methods In this retrospective single-center study, we analyzed data from 106 GBM patients treated between 2016 and 2020 at the University Hospital Halle. We examined the effects of DEX on OS and PFS during the preoperative, postoperative, and adjuvant therapy phases using Kaplan-Meier and Cox regression analyses. Cutoff analyses identified phase-specific DEX dose thresholds. Results Preoperatively, DEX had no significant effect on OS (HR: 0.998, p = 0.379) or PFS (HR: 0.998, p = 0.373), though a positive trend is possible. Postoperatively, DEX was associated with improved OS (HR: 0.995, p = 0.017) and PFS (HR: 0.995, p = 0.029). Conversely, during adjuvant therapy, higher DEX doses trended toward worse OS (HR: 1.001, p = 0.069) and PFS (p = 0.258). Patients not receiving DEX during adjuvant therapy had significantly longer OS (17.9 vs. 6.4 months, p < 0.001) and PFS (9 vs. 4.6 months, p = 0.007). Conclusion DEX influences survival outcomes differently across treatment phases. Higher doses may be beneficial pre- and postoperatively but detrimental during adjuvant therapy. These findings underscore the importance of phase-specific DEX dosing and support further research into optimal corticosteroid strategies in GBM care.
Göbel et al. (Thu,) studied this question.