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The HALLMOUNT Score: Development of a Novel Multidimensional Prognostic Model for Solid Tumors, with Initial Clinical
Ahmet Unlu1, Asim Armagan Aydin1, Banu Ozturk1
1Department of Clinical Oncology, University of Health Sciences, Antalya Education and Research Hospital, 07100 Antalya, Turkey.
Medicina (Kaunas, Lithuania)
|December 31, 2025
Summary
The new HALLMOUNT score, integrating nine blood and clinical markers, effectively predicts survival in aggressive grade 4 diffuse gliomas. This simple index aids in risk stratification for patients with these challenging brain tumors.
Area of Science:
- Neuro-oncology
- Biomarker Discovery
- Clinical Prognostics
Background:
- Grade 4 adult-type diffuse gliomas are aggressive CNS malignancies with limited prognostic tools.
- Molecular classification is key, but integrating systemic host response is crucial for better prediction.
Purpose of the Study:
- To introduce and validate the HALLMOUNT score, a multidimensional prognostic index for grade 4 adult-type diffuse gliomas.
- To assess the score's ability to integrate tumor biology and host response for improved prognostication.
Main Methods:
- Retrospective analysis of 227 patients with grade 4 adult-type diffuse glioma.
- The HALLMOUNT score incorporates nine pretreatment variables: hemoglobin, albumin, LDH, lymphocyte, monocyte, ECOG, uric acid, neutrophil, and thrombocyte counts.
- ROC analyses and Cox regression models were used to evaluate prognostic performance for OS and PFS.
Main Results:
- High HALLMOUNT scores (≥2.5) correlated with older age, comorbidities, poor ECOG status, IDH-wild phenotype, lower resection rates, and reduced treatment response.
- The HALLMOUNT score demonstrated predictive accuracy comparable to existing markers (AUC = 0.650).
- High scores independently predicted significantly inferior overall survival (OS) and progression-free survival (PFS).
Conclusions:
- The HALLMOUNT score is a simple, cost-effective biomarker reflecting tumor aggressiveness and host vulnerability in diffuse gliomas.
- It allows for refined risk stratification and supports individualized therapeutic planning.
- Prospective validation in diverse cohorts is warranted.

