Skip to content

Role of PET/CT With Fluorine-18 Tracers of Bone Metastases in Prostate Cancer

Role of PET/CT With Fluorine-18 Tracers and of Diffusion Weighted Whole-body MRI in the Early Detection of Bone Metastases in Prostate Cancer

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT01501630
Acronym
FLUPROSTIC
Enrollment
112
Registered
2011-12-29
Start date
2011-12-31
Completion date
2014-12-31
Last updated
2015-10-14

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

Conditions

Prostate Cancer

Keywords

Comparison of imaging modalities, Impact on patient management, Optimisation of cost of the diagnostic strategy

Brief summary

Compare PET/CT and MRI for the early detection of bone metastases of prostate cancer: diagnostic performance and impact on the patient management.Determine the lowest cost strategy according to the precise clinical circumstances.

Detailed description

In patients with high risk prostate cancer and high PSA levels, PET/CT with fluoride (18F) and FLUOROCHOLINE (18F) and whole-body MRI will be performed within one month. Data of a 6 month follow-up after those examination will be made available to a panel of independent experts. They will determine the standard of truth (SOT) concerning the invasion of the skeleton and also of soft tissue by prostate cancer tissue, the impact of each imaging modality on patient management and the adequacy of the decisions. In some cases (anti-hormone treatment without histology), it will not be possible to determine the SOT. By comparison of the results of blind readings for each imaging modality with the standard of truth, the diagnostic performance will be determined. By simulation, several strategies will be constructed concerning the best examinations to be performed and the sequence according to the precise clinical circumstances. Their cost and effectiveness will be evaluated.

Interventions

DEVICEperformance of PET/CT and whole-body MRI

For PET/CT radiopharmaceuticals, both registered in France:Fluoride (18F)FLUOROCHOLINE (18F)No contrast agent scheduled for MRI in the study RadiopharmaceuticalsSingle use, 2-4 MBq/kg body weight, IV infusion

Sponsors

Assistance Publique - Hôpitaux de Paris
Lead SponsorOTHER

Study design

Time perspective
PROSPECTIVE

Eligibility

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

Inclusion criteria

* Age \> 18 * Histologically proven prostate cancer. * Abnormal plasmatic level of prostate specific antigen dating less than 3 months, initial Gleason score available * Written informed consent.

Exclusion criteria

* Other active cancer or bone infection. * Chemotherapy or change in hormone therapy since the last PSA assay * Contraindication to MRI without contrast agent (claustrophobia, pace maker, metallic foreign body, some cardiac valves). Metallic joint prostheses are NOT a contraindication. * Allergic reaction to radiopharmaceuticals that will be used. * Patient who seems not capable of staying in the gantry of the machines during the examinations without moving.

Design outcomes

Primary

MeasureTime frameDescription
bone metastaseswithin 6 monthsFollow up data (histology, imaging, PSA levels) during 6 months to determine the standard of truth and the adequacy of the management decided on basis of imaging modalities.

Countries

France

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 28, 2026