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18F-DOPA-PET in Non-tumoral and Tumoral Brain Lesions

18F-DOPA-PET in Non-tumoral and Tumoral Brain Lesions

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT04306484
Acronym
FDOPA
Enrollment
74
Registered
2020-03-13
Start date
2020-01-01
Completion date
2020-12-31
Last updated
2025-12-04

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

Conditions

Brain Tumor

Keywords

tumor, tumoral, non-tumoral, pseudotumoral, 3,4-dihydroxy-6-[18F]-fluoro-L-phenylalanine, FDOPA, positron emission tomography, PET

Brief summary

Background: 3,4-dihydroxy-6-\[18F\]-fluoro-L-phenylalanine (FDOPA) positron emission tomography (PET) can identify well low and high grade brain tumors. However, increased FDOPA uptake has been reported in non-tumoral brain lesions. The aim was to analyse FDOPA-PET in patients with non-tumoral brain lesions and to compare them with patients with (low and high grade) brain tumors. Methods: retrospective analyse. Patients consecutively recruited with suspected primary brain tumor (based on clinical and MRI findings) referred for FDOPA-PET at Nimes university Hospital between June 2015 and June 2019. FDOPA-PET parameters (maximum and mean lesion standardized uptake values \[SUV\] and ratios comparing lesion with different background uptake SUV) and thresholds were analysed in search for those offering optimal discrimination between non-tumoral and tumoral lesions.

Interventions

DIAGNOSTIC_TESTFDOPA-TEP

FDOPA-TEP performed as part of the normal management of a suspected brain tumour

Sponsors

Centre Hospitalier Universitaire de Nīmes
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
RETROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* presence of defined tumor (histology was required) or non-tumor (diagnosed by histological or other analyses) diagnosis, * clinical and MRI follow-up of \>24 months, * FDOPA-PET scan \<2 months before surgery or stereotactic biopsy (when performed)

Design outcomes

Primary

MeasureTime frameDescription
FDOPA-TEPDay 1analyse of FDOPA-PET parameters (maximum and mean lesion standardized uptake values \[SUV\] and ratios comparing lesion with different background uptake SUV)

Countries

France

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 25, 2026