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Updated: Aug 5, 2026

Quantitative Immunohistochemistry of the Cellular Microenvironment in Patient Glioblastoma Resections
Published on: July 31, 2017
Beyond morphology: imaging the glioblastoma microenvironment in the era of quantitative neuro-oncology
Lorenzo Arena1, Giuseppe Espa2, Giovanni Bertalot1
1Centre for Medical Sciences (CISMed), University of Trento, Trento, Italy.
Abstract:
Glioblastoma (GBM) is the most aggressive primary brain tumor in adults and is characterized by rapid progression, marked spatial and molecular heterogeneity, and poor prognosis despite multimodal treatment strategies. Tumor behavior is not determined solely by intrinsic genetic alterations but also by dynamic interactions within the tumor microenvironment, including hypoxia, aberrant angiogenesis, immune modulation, and metabolic reprogramming, which are major drivers of treatment resistance and disease recurrence. Magnetic resonance imaging (MRI) remains the cornerstone of diagnosis and treatment planning; advanced quantitative techniques have expanded its role beyond structural assessment, enabling in vivo characterization of tissue cellularity, vascular architecture, perfusion, and microenvironmental dynamics. Positron Emission Tomography (PET) provides complementary metabolic and molecular information, improving tumor delineation, detection of infiltrative disease, and assessment of hypoxia and treatment response. PET-MRI integration within a multimodal framework enables spatially resolved mapping of tumor heterogeneity and microenvironmental niches that cannot be adequately assessed by either modality alone. Radiomics and radiogenomics approaches further enhance this paradigm by extracting quantitative imaging features that reflect underlying biological processes and linking imaging phenotypes with molecular and clinical outcomes. Artificial Intelligence enables automated feature extraction, multimodal data integration, and predictive modeling for diagnosis, prognosis, and treatment response assessment. Despite these advances, clinical translation remains limited by methodological heterogeneity, lack of standardized acquisition protocols, and insufficient prospective validation. Future research should prioritize harmonized multicenter studies and biologically informed multimodal analytical frameworks to enable the routine implementation of microenvironment-oriented precision imaging in GBM management.
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