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Evaluation of the Use of Radiomics in 18F-FDOPA PET Examinations for the Characterization of Gliomas

Evaluation of the Use of Radiomics in 18F-FDOPA PET Examinations for the Characterization of Gliomas

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT04469244
Acronym
RADDOPAG
Enrollment
1000
Registered
2020-07-14
Start date
2020-07-01
Completion date
2020-10-20
Last updated
2026-06-25

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Study on the Use of Radiomics in Gliomas of Initial Disgnosis

Keywords

18F-FDOPA, Glioma, Radiomics

Brief summary

The evaluation of gliomas in imaging represents a real challenge today, at the initial diagnosis, for therapeutic planning or follow-up treatment of these lesions. There is an urgent need for non-invasive imaging tools to evaluate a glioma throughout its management. At present, the diagnosis of certainty is only obtained through an anatomo-pathological analysis with sampling during an invasive procedure (surgery or biopsy). Magnetic resonance imaging, through perfusion, diffusion imaging or spectroscopy is developing in gliomas. However, it remains time-consuming and is not always available. At the same time, positron emission tomography (PET) with amino acids is an interesting alternative for these brain tumours. Amino acid PET has the advantage of being more specific than the abnormalities detected in MRI and the amino acid radiotracers cross the blood-brain barrier, even if not broken, unlike Gadolinium in MRI. Among these radiotracers, 18F-FDOPA can, among other things, assist in the non-invasive staging of gliomas at initial diagnosis.

Interventions

None listed

Sponsors

Central Hospital, Nancy, France
Lead SponsorOTHER

Study design

Observational model
CASE_ONLY
Time perspective
RETROSPECTIVE

Eligibility

Sex/Gender
ALL

Inclusion criteria

* Patient having performed a PET/CT examination at 18F-FDOPA for his glioma in the nuclear medicine department of the CHRU de Brabois for which the raw data are available; * Person who received full information on the organization of the research and did not object to the use of these data; * Patients affiliated to a social security scheme

Exclusion criteria

* \- Person who received full information on the organization of the research and who objected to the use of the data * Adult person subject to a legal protection measure (guardianship, curatorship, safeguard of justice). * A person of full age who is unable to give consent and who is not subject to a legal protection measure.

Design outcomes

Primary

MeasureTime frameDescription
Diagnostic performance (sensitivity, specificity, accuracy) of parameters extracted from radiomic analysis to predict the molecular characteristics of gliomas at initial diagnosis.1 yearEvaluating the performance of radiomics use in gliomas at initial diagnosis

Secondary

MeasureTime frameDescription
Diagnostic performance (sensitivity, specificity, accuracy) of parameters extracted from radiomic analysis to predict glioma recurrence1 yearAssessing the performance of radiomics use in the search for glioma recurrence
Diagnostic performance (sensitivity, specificity, accuracy) of parameters extracted from radiomic analysis to predict the response to glioma treatments.1 yearEvaluating the performance of the use of radiomics in the follow-up of glioma disease treatments
Comparison of dynamic parameters (time to peak, slope, area under curve) obtained with different reconstruction parameters versus dynamic parameters obtained on digital phantom from literature data6 monthsOptimization of dynamic analysis for the interpretation of the PET/CT examination at 18F-FDOPA

Countries

France

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Jun 26, 2026