Recent studies have significantly advanced our understanding of glioblastoma (GBM) biology and treatment strategies. One notable finding is the identification of a unique population of tumor-associated neutrophils (TANs) that exhibit dendritic-like features, which have been shown to accumulate within tumors and suppress tumor growth in vivo. This 'hybrid' phenotype, distinct from traditional cytotoxic TANs, suggests a potential role for these cells in modulating immune responses against GBM (ref: Lad doi.org/10.1016/j.ccell.2024.08.008/). In contrast, research on anti-CSF-1R therapy indicates that while targeting tumor-associated macrophages can initially regress tumors and improve survival, a fibrotic response may lead to recurrence in approximately 50% of cases, highlighting the complexity of GBM treatment (ref: Watson doi.org/10.1016/j.ccell.2024.08.012/). Furthermore, a high-throughput screening of neuroactive drugs has revealed promising candidates with potent anti-GBM activity, emphasizing the need for innovative therapeutic approaches beyond conventional DNA-alkylating agents (ref: Lee doi.org/10.1038/s41591-024-03224-y/). Additionally, the exploration of GABAergic neuronal lineage in diffuse hemispheric gliomas has uncovered potential actionable targets, suggesting that understanding tumor origin may inform future therapies (ref: Liu doi.org/10.1016/j.ccell.2024.08.006/). Overall, these findings underscore the multifaceted nature of glioblastoma and the necessity for a diverse therapeutic arsenal to combat its recurrence and resistance.