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Updated: May 25, 2026

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Published on: February 17, 2023
Imaging modalities in high-grade gliomas: pseudoprogression, recurrence, or necrosis?
1Department of Medical Oncology, Royal Melbourne Hospital, Grattan Street, Parkville, Victoria 3050, Australia.
Detecting high-grade glioma (HGG) recurrence is difficult due to therapy-related changes. Conventional MRI and (18)F-FDG PET show sensitivity, while thallium SPECT offers specificity in distinguishing progressive disease from pseudoprogression or radiation necrosis.
Area of Science:
- Neuro-oncology
- Radiology
- Nuclear Medicine
Background:
- High-grade gliomas (HGG) often recur post-treatment, posing diagnostic challenges.
- Therapy-induced changes like pseudoprogression (PP) and radiation necrosis (RN) can mimic progressive disease (PD) on imaging.
- Accurate differentiation is crucial for appropriate patient management.
Purpose of the Study:
- To review existing literature on imaging modalities for differentiating HGG progressive disease (PD) from pseudoprogression (PP) and radiation necrosis (RN).
- To assess the sensitivity and specificity of various imaging techniques in this differentiation.
Main Methods:
- A comprehensive literature review was conducted, analyzing 26 articles.
- Studies compared the diagnostic value of different imaging modalities, including MRI, PET, and SPECT.
Main Results:
- Conventional MRI and (18)fluorine-fluorodeoxyglucose positron emission tomography ((18)F-FDG PET) demonstrated higher sensitivity in differentiating PD from PP and RN.
- (18)F-FDG PET showed promise in detecting metabolic changes associated with tumor activity.
- Thallium single photon emission CT (SPECT) exhibited greater specificity in distinguishing PD from PP and RN.
Conclusions:
- Both MRI and (18)F-FDG PET are sensitive tools for detecting potential HGG progression.
- Thallium SPECT provides higher specificity for differentiating true progression from treatment effects.
- Further prospective studies are essential to determine the optimal diagnostic imaging strategy for HGG recurrence.
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