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| Name | Class |
|---|---|
| Unité de Recherche Clinique Necker Cochin, Fr | UNKNOWN |
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The purpose of this study is to determine if trans-rectal microwave ablation of the index tumor of patients with low-risk prostate cancer is sufficiently precise and safe, using MRI-transrectal ultrasound image registration.
In men with low-risk prostate cancer, European and American guidelines recommend either active surveillance or whole-gland treatments, with significant induced morbidity and burden on quality of life. Focal treatments of the index tumor are currently under investigation to decrease morbidity while proposing active treatment.
The purpose of this study is to determine the feasibility, precision and safety of a novel ablation treatment using microwaves, delivered transrectally under real-time guidance with MRI-transrectal ultrasound image registration. The index tumor will be detected with prostate MRI and characterized with targeted biopsies using MRI-transrectal ultrasound image registration. It will then be ablated with microwaves using the same transrectal approach and guidance system (KOELIS).
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| Label | Type | Description | Intervention Names |
|---|---|---|---|
| Microwave | Experimental | Microwave trans rectal focal treatment |
|
| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| Microwave trans rectal focal treatment | Device | Microwave trans-rectal ablation of the prostatic index tumor using MRI-transrectal ultrasound image registration |
|
| Measure | Description | Time Frame |
|---|---|---|
| Complete necrosis of the index tumor on prostate MRI | 7 days |
| Measure | Description | Time Frame |
|---|---|---|
| Margins of necrosis around the index tumor on prostate MRI | 7 days | |
| Erectile and Ejaculatory function using the International Index Erectile Function (IIEF) self questionnaire | to assess sexual tolerance |
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Inclusion Criteria:
Patients aged from 45 to 76 years old ;
Life expectancy above 10 years ;
Diagnosis of prostate cancer confirmed on prostate biopsies ;
Low risk of progression, defined with D'Amico criteria :
Detection of the index tumor with prostate MRI, characterized with targeted biopsies using MRI-transrectal ultrasound image registration ;
Patient accepting to be followed after the procedure using active surveillance protocol standards ;
Patient affiliated to national health care insurance ;
Free consent, informed and written, dated and signed by the patient and the investigator before enrollment.
Exclusion Criteria:
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| Name | Affiliation | Role |
|---|---|---|
| Nicolas BARRY DELONGCHAMPS, MD, PhD | Assistance Publique - Hôpitaux de Paris | Principal Investigator |
| Facility | Status | City | State | ZIP | Country | Contacts |
|---|---|---|---|---|---|---|
| Assistance Publique - Hôpitaux de Paris | Paris | Paris | France |
| PubMed Identifier | Type | Citation | Retractions |
|---|---|---|---|
| 34260598 | Result | Barry Delongchamps N, Schull A, Anract J, Abecassis JP, Zerbib M, Sibony M, Jilet L, Abdoul H, Goffin V, Peyromaure M. Feasibility and safety of targeted focal microwave ablation of the index tumor in patients with low to intermediate risk prostate cancer: Results of the FOSTINE trial. PLoS One. 2021 Jul 14;16(7):e0252040. doi: 10.1371/journal.pone.0252040. eCollection 2021. |
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| ID | Term |
|---|---|
| D009369 | Neoplasms |
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|
| 7 days |
| Erectile and Ejaculatory function using the International Index Erectile Function (IIEF) self questionnaire | to assess sexual tolerance | 1 month |
| Erectile and Ejaculatory function using the International Index Erectile Function (IIEF) self questionnaire | to assess sexual tolerance | 3 months |
| Erectile and Ejaculatory function using the International Index Erectile Function (IIEF) self questionnaire | to assess sexual tolerance | 6 months |
| Urinary symptoms using IPSS | to assess urinary tolerance | 7 days |
| Urinary symptoms using IPSS | to assess urinary tolerance | 1 month |
| Urinary symptoms using IPSS | to assess urinary tolerance | 3 months |
| Urinary symptoms using IPSS | to assess urinary tolerance | 6 months |
| Number of cancer on targeted biopsies within the treated volume | to assess oncological efficacy | 6 months |