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Updated: Jan 16, 2026

Digital Spatial Profiling for Characterization of the Microenvironment in Adult-Type Diffusely Infiltrating Glioma
Published on: September 13, 2022
CMRO2 (DSC-PW) perfusion parameter helps to distinguish between progression and pseudoprogression in patients with
Emanuele Tommasino1, François Ducray2, Antoine Seyve2
1Department of Neuroradiology, Pierre Wertheimer Hospital, Hospices Civils de Lyon, Lyon, France. Emanuele.tommasino@gmail.com.
Objective:
To evaluate the diagnostic accuracy of CMRO2 (cerebral metabolic rate of oxygen) in differentiating between pseudoprogression and true tumour progression in patients with glioblastoma (GB) following chemoradiotherapy and to compare its performance with rCBV (relative cerebral blood volume).
Materials And Methods:
This diagnostic accuracy study included two cohorts: an analysis group (32 patients, 19 progression, 13 pseudoprogression) and a validation group (52 patients, 35 progression, 17 pseudoprogression). Patients underwent MRI (magnetic resonance imaging) with DSC (dynamic susceptibility contrast) and DCE (dynamic contrast-enhanced) perfusion imaging. CMRO2 and rCBV thresholds were evaluated to calculate sensitivity, specificity, and area under the curve (AUC). Inclusion criteria were GB diagnosis, standard chemoradiotherapy, and new or enlarged enhancing lesions on MRI within one year.
Results:
In the analysis group (mean age, 60.8 ± 8 years), CMRO2 showed superior performance with an AUC of 0.89 (95% CI 0.77-0.98), sensitivity of 84.2%, and specificity of 83.3%. rCBV achieved an AUC of 0.63 (95% CI 0.42-0.88). In the validation group (mean age, 63 ± 7 years), CMRO2 maintained an AUC of 0.91 (95% CI 0.82-0.98), while rCBV reached an AUC of 0.79 (95% CI 0.65-0.91). The DeLong test confirmed CMRO2's significantly higher performance (p = 0.04).
Conclusion:
CMRO2 demonstrates higher diagnostic performance than rCBV in distinguishing pseudoprogression from true progression in GB patients. Despite limitations, CMRO2 shows promise as a non-invasive biomarker, warranting further multicentre validation.

