Jade Apolline Robert
Current Organizations / Institutes
The organizations/institutes from the scholar's latest article
Research Subjects
Research Interests
Jade Apolline Robert has a total of 5 co-authors. Here are the top co-authors by number of shared publications:
- Arthur Leclerc
CHU de Caen – Department of Neurosurgery, Service de Neurochirurgie, Caen, France
1 shared publication - Denis Agostini
Department of Nuclear Medicine, CHU Caen and Normandy University, EA 4650, Caen, France.
1 shared publication - Evelyne Emery
Department of Neurosurgery, Caen University Hospital, Caen, France
1 shared publication - Jonathan Vigne
Department of Nuclear Medicine, CHU de Caen Normandie, Normandie Université, UNICAEN, 14000 Caen, France
1 shared publication - Mathilde Ducloie
Department of Medical Oncology, François Baclesse Comprehensive Cancer Center, Caen, France
1 shared publication
Latest Publications
- Open Access
- 18 September 2024
- Published by MDPI AG in Pharmaceuticals
- Vol. 17 (9) , 1228
Contribution of [18F]FET PET in the Management of Gliomas, from Diagnosis to Follow-Up: A Review
Gliomas, the most common type of primary malignant brain tumors in adults, pose significant challenges in diagnosis and management due to their heterogeneity and potential aggressiveness. This review evaluates the utility of O-(2-[18F]fluoroethyl)-L-tyrosine ([18F]FET) positron emission tomography (PET), a promising imaging modality, to enhance the clinical management of gliomas. We reviewed 82 studies involving 4657 patients, focusing on the application of [18F]FET in several key areas: diagnosis, grading, identification of IDH status and presence of oligodendroglial component, guided resection or biopsy, detection of residual tumor, guided radiotherapy, detection of malignant transformation in low-grade glioma, differentiation of recurrence versus treatment-related changes and prognostic factors, and treatment response evaluation. Our findings confirm that [18F]FET helps delineate tumor tissue, improves diagnostic accuracy, and aids in therapeutic decision-making by providing crucial insights into tumor metabolism. This review underscores the need for standardized parameters and further multicentric studies to solidify the role of [18F]FET PET in routine clinical practice. By offering a comprehensive overview of current research and practical implications, this paper highlights the added value of [18F]FET PET in improving management of glioma patients from diagnosis to follow-up.
- 18 September 2024
- Published by MDPI AG in Pharmaceuticals
- Vol. 17 (9) , 1228
Open AccessContribution of [18F]FET PET in the Management of Gliomas, from Diagnosis to Follow-Up: A Review
Gliomas, the most common type of primary malignant brain tumors in adults, pose significant challenges in diagnosis and management due to their heterogeneity and potential aggressiveness. This review evaluates the utility of O-(2-[18F]fluoroethyl)-L-tyrosine ([18F]FET) positron emission tomography (PET), a promising imaging modality, to enhance the clinical management of gliomas. We reviewed 82 studies involving 4657 patients, focusing on the application of [18F]FET in several key areas: diagnosis, grading, identification of IDH status and presence of oligodendroglial component, guided resection or biopsy, detection of residual tumor, guided radiotherapy, detection of malignant transformation in low-grade glioma, differentiation of recurrence versus treatment-related changes and prognostic factors, and treatment response evaluation. Our findings confirm that [18F]FET helps delineate tumor tissue, improves diagnostic accuracy, and aids in therapeutic decision-making by providing crucial insights into tumor metabolism. This review underscores the need for standardized parameters and further multicentric studies to solidify the role of [18F]FET PET in routine clinical practice. By offering a comprehensive overview of current research and practical implications, this paper highlights the added value of [18F]FET PET in improving management of glioma patients from diagnosis to follow-up.