university Hospital Grenoble
Grenoble, 38043, France
NCT Number: NCT07355504
The rationale of the PROCEDE trial is to explore a novel early detection strategy in which biopsy decision does not rely on one single MRI examination, but on the progression of the MRI lesion between 2 consecutive exams, with the objective of reducing the number of unnecessary biopsies, detection of non-clinically prostate cancer and, ultimately, overtreatment.
Trial opening soon.
Get Notified18 year and older
Male
Interventional
Not applicable
Grenoble, 38043, France
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
Patients randomized to the experimental arm will proceed with MRI surveillance. A follow-up visit is planned at 6 months with the result of a PSA test, and it is possible at each investigator's discretion, to prescribe the follow-up MRI at 6 months in case of rising PSA. Otherwise, the repeat MRI will be scheduled one year after the initial MRI. Images will also be sent to the coordinating center for central reviewing of the new MRI exam and assessment of progression.
Time frame: at 2 years
To evaluate the impact of a novel early detection strategy based on serial MRI exams, compared to the standard of care, on the rate of definitive treatment for localized prostate cancer
Time frame: at 5 years.
Time to the first event among (i) definitive treatment for localized prostate cancer, defined as one of the following procedures: radical prostatectomy, radiotherapy, brachytherapy, focal therapy; (ii) occurrence of prostate cancer metastases; (iii) all-cause death, occurring between randomization and 5-year follow-up.
Time frame: at 2 years and 5 years.
Number of biopsy procedures performed.
Time frame: at 2 years and 5 years.
Choice of definitive treatment, if applicable, among the following options: (i) brachytherapy, (ii) focal therapy, and (iii) unimodal therapy.
Time frame: at 2 years and 5 years.
Adverse pathological criteria (pT3, pN1, detectable PSA) in patients treated with radical prostatectomy.
Time frame: at 2 years and 5 years.
Biochemical recurrence-free survival, disease-specific survival (i.e., censoring non-disease-related deaths), and overall survival.
Time frame: at 5 years
HADS scale, MAX-PC questionnaire, EPIC-26 questionnaire, EQ-5D-5L questionnaire.
The combination of these questionnaires will allow us to assess the level of anxiety and the quality of life of patients treated with the new strategy; we have decided to use them together for a combined evaluation.
Time frame: at 5 years.
ICUR. The incremental cost-utility ratio (ICUR) will be calculated by dividing the mean difference in costs by the mean difference in QALYs (estimated from the EQ-5D-5L). The ratio will be expressed as cost per healthy life-year gained.
Time frame: at 5 years
Database collecting all MRI examinations in DICOM format, along with oncologic outcomes (progression/no progression).
Contact information is provided by the study sponsor or research team.
Assilah AB bouzit
CONTACT
0476767971 ext. +33
Gaelle GF FIARD, Professor
CONTACT
0476767971 ext. +33
University Hospital, Grenoble
Other
Acronym: PROCEDE
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