Interest of Trimodality PET-CT Choline MRI Before Radiotherapy in High Risk Prostate Cancer
NCT ID: NCT03734757
Last Updated: 2026-01-02
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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COMPLETED
NA
20 participants
INTERVENTIONAL
2019-02-14
2020-12-10
Brief Summary
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For this type of cancer, reference treatment is radiotherapy combined with hormone therapy.
The added value of MRI in the delineation of volumes for radiotherapy is known, especially for the definition of extra-prostatic extensions and prostatic apex. However, its regular use is difficult. Indeed, acquisition of Magnetic Resonance Imaging parameters for diagnostic are not adapted to be fused with the planning Computed Tomography.
The literature shows that Positron Emission Tomography-Computed Tomography with Fluorocholine is better in terms of diagnostic performance compared to bone scan for bone metastases and to pelvic Magnetic Resonance Imaging for nodal extension.
It would therefore improve staging for these patients with a high risk of locoregional and metastatic invasion even if its use is currently not recommended in the initial staging.
Thanks to Magnetic Resonance Imaging acquisition parameters adapted to Radiotherapy and additional functional information, an acquisition in tri-modality Positron Emission Tomography/computed Tomography/ Magnetic Resonance Imaging could have an impact on the volumes definition for radiotherapy or even on the therapeutic strategy.
The aim of the study is to evaluate the volume modifications obtained on the trimodality evaluation, compared to the standard initial staging (geometric comparison).
In addition, it would be a preliminary study for a project using Prostate-specific membrane antigen (PSMA) in trimodality, and / or for a therapeutic interventional study.
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Detailed Description
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External radiotherapy combined with prolonged hormone therapy is the reference treatment for these cancers.
Radiotherapy requires a planning Computed Tomography. Magnetic Resonance Imaging is known to be better for definition of extra-prostatic extensions and prostatic apex. However, its regular use is difficult for the radiotherapy planning.
Moreover, Positron Emission Tomography-Computed Tomography with Fluorocholine detects earlier nodal and bone metastasis.
Hypothesis: A single planning acquisition in trimodality in radiotherapy position should improve simultaneously the initial staging and the volume delineation for radiotherapy.
Main objective: Main objective is to compare volumes delineation (prostatic target and organ at risk) thanks to geometric index (Jaccard, Dice and overlap), got by trimodality and by standard initial staging and planning Computed Tomography.
Expected results: Thanks to literature data, it can be expected that prostatic delineation target volume will significantly decrease with Magnetic Resonance Imaging.
Furthermore, thanks to Positron Emission Tomography-Computed Tomography with Fluorocholine, radiotherapy planning would be different, detecting 14% of nodal extension and 7% of bone metastasis.
Finally, with trimodality the investigators expect a smaller prostate volume and a higher detection of metastatic lymph node or bone metastasis.
Then, the investigators expect an improvement of the management of patients by:
* Detecting more nodal or bone metastasis and avoiding a useless local treatment by radiotherapy
* Improving prostatic target volume delineation and allowing a better protection of organ at risk.
Conditions
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Study Design
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NA
SINGLE_GROUP
OTHER
NONE
Study Groups
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Trimodality
PET-CT with fluorocholine and MRI
imaging in trimodality
PET-CT and MRI
Interventions
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imaging in trimodality
PET-CT and MRI
Eligibility Criteria
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Inclusion Criteria
* prostate cancer : High risk (according to D'Amico Classification)
* and/or Node positive on MRI
* T2c-T3 on MRI
* with staging assessment
* will receive radiotherapy
Exclusion Criteria
* contraindication to MRI
* participation in an another therapeutic trial
* patients under guardianship or curatorship
18 Years
MALE
No
Sponsors
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Centre Henri Becquerel
OTHER
Responsible Party
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Locations
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Centre Henri Becquerel
Rouen, , France
Countries
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Other Identifiers
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CHB18.02
Identifier Type: -
Identifier Source: org_study_id
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