BIOM-82. GLIOBLASTOMA BEYOND THE ENHANCING TUMOR MARGINS: A LONGITUDINAL CASE STUDY COMPARING FET PET WITH MRI-BASED AI INFILTRATION MAPS

Abstract BACKGROUND Glioblastoma is the most common malignant brain tumor, with rapid proliferation, diffuse infiltration, and poor prognosis. Imaging plays a central role in its diagnosis, treatment planning, and disease monitoring. Positron Emission Tomography with O-(2-[18F]fluoroethyl)-L-tyrosine (FET PET) depicts metabolically active tumor irrespective of the blood-brain barrier integrity. Here, we compare FET PET with AI-generated infiltration maps (AI-InfM) derived from multiparametric MRI (mpMRI - T1, T1Gd, T2, T2-FLAIR, DSC) to identify viable tumor beyond the enhancing tumor, potentially corresponding to early recurrence sites. METHODS We identified a patient with a newly-diagnosed glioblastoma in a non resectable eloquent area. Pre-operative scans were acquired at baseline and two follow-up timepoints, during and post-treatment, at six-month intervals. Each scanning session comprised a 50-minute dynamic FET PET scan and mpMRI performed at Research Center Juelich, Germany. AI-InfM, based on Support Vector Machines, were trained following within-patient, self-normalized measures of heterogeneity across pre-operative mpMRI of treatment-naïve glioblastoma in a subset of the public UPENN-GBM dataset. AI-InfM were then generated for the identified patient and compared with FET PET visually and quantitatively using clinically-established measures, e.g., tumor-to-brain ratios (TBR). RESULTS Although FET PET showed no increased tracer uptake at baseline, the AI-InfM identified a region with elevated signal. This region exhibited increased uptake of FET in the first follow-up scan (TBRmax from 1.9 at baseline to 2.2 at follow-up), supporting the AI-InfM’s early prediction. After completion of adjuvant temozolomide therapy, the third scan denoted the predicted high-risk area with reduced tumor activity across FET PET, AI-InfM, and mpMRI. CONCLUSIONS Our findings indicate potential complementary value of FET PET and mpMRI-derived AI-InfM, for early recurrence identification. This case study underscores the potential to enhance early detection of tumor progression, by virtue of the infiltrative spread in glioblastoma, and warrants continued development and evaluation in a larger multi-institutional cohort.

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Journal
Neuro-Oncology
Published
2025-11-01
DOI
https://doi.org/10.1093/neuonc/noaf201.0170
Primary Topic
Glioma Diagnosis and Treatment
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article
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article

BIOM-82. GLIOBLASTOMA BEYOND THE ENHANCING TUMOR MARGINS: A LONGITUDINAL CASE STUDY COMPARING FET PET WITH MRI-BASED AI INFILTRATION MAPS

Na Tosha Gatson, Matthew Pease, Peter S. LaViolette, Christos A. Davatzikos et al.
Neuro-Oncology
Glioma Diagnosis and Treatment
article

BIOM-82. GLIOBLASTOMA BEYOND THE ENHANCING TUMOR MARGINS: A LONGITUDINAL CASE STUDY COMPARING FET PET WITH MRI-BASED AI INFILTRATION MAPS

Na Tosha Gatson, Matthew Pease, Peter S. LaViolette, Christos A. Davatzikos, Spyridon Bakas, Norbert Galldiks, Karl‐Josef Langen, N. Jon Shah, Hamed Akbari, Jason G. Parker, Philipp Lohmann, Sanyukta Adap, Carla Pitarch-Abaigar, Alexandra Flinn
article en

Abstract

Abstract BACKGROUND Glioblastoma is the most common malignant brain tumor, with rapid proliferation, diffuse infiltration, and poor prognosis. Imaging plays a central role in its diagnosis, treatment planning, and disease monitoring. Positron Emission Tomography with O-(2-[18F]fluoroethyl)-L-tyrosine (FET PET) depicts metabolically active tumor irrespective of the blood-brain barrier integrity. Here, we compare FET PET with AI-generated infiltration maps (AI-InfM) derived from multiparametric MRI (mpMRI - T1, T1Gd, T2, T2-FLAIR, DSC) to identify viable tumor beyond the enhancing tumor, potentially corresponding to early recurrence sites. METHODS We identified a patient with a newly-diagnosed glioblastoma in a non resectable eloquent area. Pre-operative scans were acquired at baseline and two follow-up timepoints, during and post-treatment, at six-month intervals. Each scanning session comprised a 50-minute dynamic FET PET scan and mpMRI performed at Research Center Juelich, Germany. AI-InfM, based on Support Vector Machines, were trained following within-patient, self-normalized measures of heterogeneity across pre-operative mpMRI of treatment-naïve glioblastoma in a subset of the public UPENN-GBM dataset. AI-InfM were then generated for the identified patient and compared with FET PET visually and quantitatively using clinically-established measures, e.g., tumor-to-brain ratios (TBR). RESULTS Although FET PET showed no increased tracer uptake at baseline, the AI-InfM identified a region with elevated signal. This region exhibited increased uptake of FET in the first follow-up scan (TBRmax from 1.9 at baseline to 2.2 at follow-up), supporting the AI-InfM’s early prediction. After completion of adjuvant temozolomide therapy, the third scan denoted the predicted high-risk area with reduced tumor activity across FET PET, AI-InfM, and mpMRI. CONCLUSIONS Our findings indicate potential complementary value of FET PET and mpMRI-derived AI-InfM, for early recurrence identification. This case study underscores the potential to enhance early detection of tumor progression, by virtue of the infiltrative spread in glioblastoma, and warrants continued development and evaluation in a larger multi-institutional cohort.

Neuro-OncologyVol. 27(Supplement_5)
Indiana University Health (US), Santa Clara University (US), Forschungszentrum Jülich (DE), University of Cologne (DE), Medical College of Wisconsin (US), Indiana Cancer Consortium (US), Laboratoire d’Imagerie Biomédicale (FR), Universitätsklinikum Aachen (DE), University Hospital Cologne (DE), Neurological Surgery (US), Indiana University Melvin and Bren Simon Comprehensive Cancer Center, Indiana University School of Medicine, Indiana University – Purdue University Indianapolis (US), University of Pennsylvania (US), RWTH Aachen University (DE)
Openalex Percentile: Top 51%
Glioma Diagnosis and Treatment
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