Identification of prognostically relevant residual tumor burden in glioblastoma after surgery: A comparative analysis of MR-based RANO resect classes vs [ <sup>18</sup> F]FET PET.
Abstract
2068 Background: Accurate assessment of postoperative residual tumor burden is critical in IDH -wildtype glioblastoma. The MRI-based RANO resect classification stratifies patients according to postoperative contrast-enhancing and non-contrast enhancing tumor volume but may underestimate metabolically active residual disease. The additional prognostic value of postoperative [¹⁸F]FET PET beyond MRI is yet unclear. Methods: This retrospective bicentric study included 140 patients with newly diagnosed IDH -wildtype glioblastoma and evaluable postoperative MRI and [¹⁸F]FET PET. Residual tumor volumes were segmented on MRI and classified according to the RANO resect system. PET-derived residual metabolic tumor volumes were defined using PET RANO 1.0 criteria. Spatial agreement between MRI- and PET-based volumes was quantified using Dice coefficients. Associations with overall survival were analyzed using Cox regression. Incremental prognostic value of PET was assessed using an imaging-only model (contrast-enhanced T1 (T1CE) vs. T1CE + PET) and a fully adjusted model including clinical covariates. Results: PET-derived residual tumor volumes exceeded MRI-defined volumes and showed low spatial concordance with MRI (Dice coefficient: 0.01–0.25) across all RANO resect classes. Postoperative PET-, T1CE-, and T2/FLAIR-derived tumor volumes were each associated with overall survival. Increasing PET-derived residual tumor burden was associated with a continuous increase in mortality risk. In multivariable Cox regression, PET-derived residual tumor volume remained independently associated with overall survival (adjusted hazard ratio 1.021 per cm³, 95% CI 1.008–1.033; ** p = 0.0024). In the imaging-only model, addition of PET improved time-dependent discrimination between 6 and 24 months (ΔAUC(t) 0.03–0.07) and increased Harrell’s C (ΔC ≈ 0.03). In the fully adjusted model, PET provided significant non-redundant prognostic information (likelihood ratio test, * p = 0.0049). Conclusions: Postoperative [¹⁸F]FET PET identifies metabolically active residual tumor not adequately captured by MRI and provides additional prognostic information beyond MRI-based assessment. Integration of PET into postoperative evaluation may refine prognostic stratification in IDH-wildtype glioblastoma.
Article Details
Journal Info
Journal of Clinical Oncology
Lippincott Williams & Wilkins
Authors (15)
Jens Blobner
Department of Neurosurgery LMU, Munich, Germany
Katharina Müller
Department of Pathology, University Medical Center Hamburg-Eppendorf, Hamburg, Germany
Michael Muether
Department of Neurosurgery, University Hospital Münster, Münster, Germany
Wolfgang Roll
Jonas Reis
Institute for Neuroradiology, LMU University Hospital, LMU Munich, Munich, Germany
Maximilian Mair
Division of Oncology, Department of Medicine I, Medical University of Vienna, Vienna, Austria
Niklas Thon
Department of Neurosurgery, Knappschaft University Hospital Bochum, Bochum, Germany
Stephan Schoenecker
Department of Radiation Oncology, LMU University Hospital, Munich, Germany
Patrick Harter
Center of Neuropathology and Prion Research, Faculty of Medicine, LMU Munich, Munich, Germany
Darius Kalasauskas
Department of Neurosurgery, LMU University Hospita, Munich, Germany
Louisa von Baumgarten
12Department of Neurosurgery, Ludwig Maximilian University, Munich, Germany
Florian Ringel
Joerg Tonn
Department of Neurosurgery, LMU University Hospital, Munich, Germany
Philipp Karschnia
Nathalie Lisa Albert
Department of Nuclear Medicine, LMU University Hospital, LMU Munich, Munich, Germany