AI for prognosis and treatment stratification in glioblastoma neurosurgery: a systematic review.
Clinical Snapshot
PICO Framework
| P — Population | Adult patients with glioblastoma (GBM) undergoing neurosurgical evaluation or treatment |
| I — Intervention | Artificial intelligence methods (machine learning, deep learning, radiomics) applied to MRI-derived and/or multimodal perioperative data |
| C — Comparator | Conventional clinical or imaging-based prognostic and stratification approaches (implicit comparator; not always explicitly stated across included studies) |
| O — Outcomes | Overall survival prediction, risk stratification, treatment-response assessment, post-treatment classification (pseudoprogression vs. true progression), recurrence/progression prediction, and molecular marker prediction |
Bottom Line
This PROSPERO-registered systematic review synthesises 30 studies examining AI applications for prognosis and treatment stratification in glioblastoma neurosurgery. The field is characterised by methodological diversity — radiomics combined with conventional machine learning dominates (43.3%), with deep learning and hybrid approaches also represented. Survival prediction is the most studied task (66.7% of studies). However, the evidence base has critical limitations: external validation is rare (16.7% of studies), heterogeneity across imaging protocols and outcome definitions is substantial, and no quantitative meta-analysis was feasible. Risk of bias was assessed using PROBAST-informed criteria, which is methodologically appropriate. The authors' conclusion that AI 'shows promise' but is not yet practice-ready is well-supported and appropriately conservative. For Australian neuro-oncologists and neurosurgeons, no TGA-approved AI prognostic tool currently exists for GBM, and this review reinforces that clinical adoption should await prospective, externally validated, and ideally multi-centre studies. This review serves as a useful landscape map for researchers designing future AI-GBM studies, but does not provide sufficient evidence to alter current surgical or oncological decision-making protocols.
Key Findings
P Value: Not reported at review level
Effect Size: No pooled effect size calculable; narrative synthesis only. Survival-focused tasks predominated (20/30 studies, 66.7%). Radiomics plus conventional ML was the most common model family (13/30, 43.3%), followed by deep learning (8/30, 26.7%) and hybrid DL+radiomics (4/30, 13.3%)
Primary Outcome: Descriptive synthesis of AI model performance across prognosis, risk stratification, treatment-response assessment, post-treatment classification, recurrence/progression prediction, and molecular prediction in GBM
Nnt Or Sensitivity: Individual study performance metrics (AUC, C-index, accuracy) not synthesised at review level; external validation achieved in only 5/30 studies (16.7%), limiting any estimate of real-world model sensitivity or specificity
Confidence Interval: Not applicable — no meta-analytic pooling performed
Clinical Application
Currently limited. AI tools for GBM prognosis and stratification are predominantly research-grade, lacking prospective validation, regulatory approval, and integration into clinical workflows. The 16.7% external validation rate indicates most models are not ready for clinical deployment. Implementation would require institutional MRI standardisation, prospective validation cohorts, and clinician training. In Australia, GBM management follows NHMRC-aligned and international guidelines, with standard-of-care comprising maximal safe surgical resection followed by Stupp protocol (temozolomide plus radiotherapy). No AI-based prognostic or stratification tools for GBM are currently TGA-approved or PBS-subsidised. The RACGP and relevant specialist colleges (RACS, RANZCR) have not yet issued guidance on AI integration in neuro-oncology. Australian neuro-oncology centres (e.g., Royal Melbourne Hospital, RBWH, RPAH) conducting GBM research may find this review useful for framing future prospective AI validation studies. The relatively small Australian GBM patient population (~1,500 new diagnoses annually) underscores the importance of multi-centre and international data sharing for adequate external validation. Adult patients with confirmed GBM (WHO Grade 4 IDH-wildtype glioma) being considered for or having undergone neurosurgical resection, where prognostic stratification, treatment planning, or post-treatment surveillance decisions are clinically relevant
Abstract
BACKGROUND: Glioblastoma (GBM) remains one of the most lethal adult primary brain tumors, and neurosurgical decision-making increasingly depends on integrating imaging, molecular, perioperative, and post-treatment data. Artificial intelligence (AI) methods have been proposed for several clinically relevant GBM tasks, but the literature remains heterogeneous and difficult to translate into practice. METHODS: We performed a PROSPERO-registered systematic review of AI, machine learning, and deep learning studies using MRI-derived and/or multimodal perioperative data in GBM for prognosis, risk stratification, treatment-response assessment, post-treatment classification, recurrence/progression prediction, and molecular prediction. Risk of bias was assessed using PROBAST-informed criteria. RESULTS: Thirty studies were included. Survival-focused tasks predominated (20/30, 66.7%), with radiomics plus conventional machine learning as the most common model family (13/30, 43.3%), followed by deep learning (8/30, 26.7%) and hybrid deep learning plus radiomics approaches (4/30, 13.3%). Validation was predominantly internal, and external validation was uncommon (5/30, 16.7%). CONCLUSIONS: AI shows promise for prognosis and treatment stratification in GBM neurosurgery, but current evidence is limited by heterogeneity, incomplete external validation, and inconsistent methodological reporting. CLINICAL TRIAL NUMBER: Not applicable.
References
- 1.Reyes, J. S., Snyder, M. H., Roguski, M., & Hadjipanayis, C. G. (2026). AI for prognosis and treatment stratification in glioblastoma neurosurgery: a systematic review. Journal of Neuro-Oncology. https://doi.org/10.3389/fonc.2026.1837357
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