Abstract Background Glioblastoma (GBM) is the most common and aggressive primary malignant brain tumor in adults, with a median overall survival (OS) rarely exceeding 15 months despite multimodal therapy. While established prognostic factors include age, Karnofsky Performance Status (KPS), and molecular features such as MGMT promoter methylation and IDH mutation status, increasing attention has focused on the role of treatment timing as a potentially modifiable prognostic determinant. In particular, Overall Treatment Time (OTT)—the number of calendar days from the first to the last radiotherapy fraction—may impact survival by enabling tumor repopulation when extended or interrupted. Methods We conducted a retrospective monocentric cohort study of 166 consecutive adult patients with histologically confirmed IDH-wild-type glioblastoma treated with standard concurrent chemoradiotherapy and adjuvant temozolomide between January 2016 and January 2024. OTT was defined as the total number of days from radiotherapy start to end, including all interruptions. A cutoff of 48 days was adopted based on prior evidence. Patients were stratified according to OTT, number and cause of radiotherapy interruptions, and molecular status (MGMT promoter methylation and EGFR amplification). The primary endpoints were OS and progression-free survival (PFS), analyzed with Kaplan–Meier and Cox regression models. Results Median OTT was 43 days (range: 40–65). Patients with OTT ≤ 48 days had a significantly longer median OS than those with OTT > 48 days (20 vs. 10 months, p = 0.003). Multivariable Cox regression confirmed OTT > 48 days as an independent negative prognostic factor (HR = 1.41, p = 0.009). Multiple interruptions, regardless of cause, further reduced OS, particularly in patients with MGMT-methylated tumors and low EGFR expression. Clinical interruptions—often due to toxicity—were associated with significantly worse outcomes than single technical interruptions. Notably, the negative impact of prolonged OTT was significantly more pronounced in the MGMT-methylated subgroup (p for interaction = 0.018), suggesting a biologically distinct vulnerability to treatment delays. Conclusions This study demonstrates that prolonged OTT and radiotherapy interruptions are independently associated with inferior survival in patients with IDH-wild-type glioblastoma, particularly in biologically favorable subgroups such as MGMT-methylated tumors. These findings underscore the importance of strict adherence to treatment schedules and minimizing avoidable delays. Molecular profiling may aid in identifying patients most vulnerable to the adverse effects of treatment prolongation, supporting a more personalized and time-sensitive approach to GBM management. Further prospective validation is warranted.
Tini et al. (Thu,) studied this question.
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