MedPath

Prostate Interstitial Brachytherapy With I125 Implant With Target Dose Supplementation in the Tumor Volume Guided by TRINITY® PERINE 3D System

Not Applicable
Recruiting
Conditions
Prostate Cancer
Interventions
Other: Interstitial Brachytherapy of the Prostate With Iodine 125 Implant With Target Dose Supplementation in the Tumor Volume Guided by the TRINITY® PERINE 3D
Registration Number
NCT05322356
Lead Sponsor
University Hospital, Grenoble
Brief Summary

The objective of the FOCUS-Boost project is to implant for the first time with a 3D ultrasound image fusion registration system (3D echo) implant of iodine 125 with precision in a target volume determined by positive biopsies.

Detailed Description

The interstitial brachytherapy procedure for the prostate does not allow for a robust focal treatment to accurately deliver additional dose to the tumour volume. FOCUS BOOST allows the precise implantation of 125 iodine implant with greater accuracy (using a 3D ultrasound image fusion registration system) in a target volume.

For this purpose, positive biopsies, performed in this research protocol, will be used prior to surgery. Prostate brachytherapy will be optimised thanks to the TRINITY® system and its guidance quality, by increasing the dose of the intra-prostate tumour volume (BOOST) without increasing the total dose delivered to the prostate. Increasing the dose to the tumour target volume could improve disease control and decrease the risk of recurrence.

Recruitment & Eligibility

Status
RECRUITING
Sex
Male
Target Recruitment
15
Inclusion Criteria
  • At least 18 years
  • Patient to be treated with brachytherapy
  • Patient with low or favorable intermediate risk prostate adenocarcinoma ISUP 1 and 2, G6 (3+3) or G7 (3+4)
  • Life expectancy of more than 10 years
  • PSA (prostate-specific antigen) < 15 ng/ml
  • cT1c or cT2a or cT2b
  • Prostate volume ≤ 60 cc
  • ECOG Performance status 0-2
  • Patient is affiliated to a health insurance system
  • Patient who has signed consent form
Exclusion Criteria
  • Patient with urinary function disorders IPSS> 14
  • Prostate volume > 60cc.
  • Gleason 7(4+3) or Gleason score ≥8
  • PSA ≥ 15 ng/ml
  • Patient with metastases
  • Hormone therapy with antiandrogen or LHRH analogue
  • History of abdominopelvic irradiation
  • Inflammatory digestive disease (haemorrhagic rectocolitis, Crohn's disease)
  • Interventional study in progress that may interfere with the present study
  • Protected persons (patient concerned by articles L1121-5, L1121-6, L1121-8 of the French public health code)

Study & Design

Study Type
INTERVENTIONAL
Study Design
SINGLE_GROUP
Arm && Interventions
GroupInterventionDescription
InterventionInterstitial Brachytherapy of the Prostate With Iodine 125 Implant With Target Dose Supplementation in the Tumor Volume Guided by the TRINITY® PERINE 3DInterstitial Brachytherapy of the Prostate With Iodine 125 Implant With Target Dose Supplementation in the Tumor Volume Guided by the TRINITY® PERINE 3D system
Primary Outcome Measures
NameTimeMethod
Implant for the first time, in a clinical situation, iodine 125 implants in a planned target volume, using a 3D echo-mapping fusion guidance system of positive biopsies.24 hours

To evaluate the number of successful/failed iodine 125 implants (BOOST implants) implanted in the CTV-boost (Clinical Target Volume) defined from the mapping of positive biopsies.

The maximum number of BOOST implant implanted will be 4 implants, depending on the size of the target:

10 mm\< target ≤ 15 mm = 2 implants; 15 mm \< target ≤ 20mm = 3 implants; 20 mm \< target ≤ 30 mm = 4 implants; Success is defined as "the centre of the implant is in the target volume". Failure is defined as "the centre of the implant is outside the target volume". The primary endpoint is evaluated on the ultrasound acquisition performed with the Trinity® Perine probe, at the end of the BOOST implant insertion procedure

Secondary Outcome Measures
NameTimeMethod
Assess toxicity (pre brachytherapy visit, M1, M3, M6, M12) with CTCAE score12 months

Assessment of toxicity by classification of toxicities according to CTCAE score (Common Terminology Criteria for Adverse Events: Grade 1 Mild / Grade 2 Moderate / Grade 3 Severe or medically significant but not immediately life-threatening / Grade 4 Life-threatening consequences / Grade 5 Death related to A

To check the absence of overdose in the prostate at D0 and M1.1 month

V150% \< 60% of prostate volume on CT dosimetry at D0 and 1 month

Assess toxicity (pre brachytherapy visit, M1, M12) with flowmetry12 months

Assessment of toxicity by urinary flowmetry

To assess the efficacy of the treatment at M6 and M12.12 months

PSA (Prostate Specific Antigen) test

Assess quality of life (inclusion, M1, M3, M6, M12).12 months

QLQ-C30 (Quality of Life Questionnaire) score

To check the absence of overdose in organs at risk (bladder, urethra, rectum) at D0 and M1.1 month

Absence of overdose in organs at risk on scanner dosimetry

Assess sexual health (inclusion, M1, M3, M6, M12).12 months

IIEF5 questionnaire score (Erectile dysfunction severe (score 5-10), moderate (11-15), mild (16-20), normal erectile function (21-25) and uninterpretable (1-4)).

Measure the duration of the complete procedure, the additional act (BOOST) and the final ultrasound acquisition performed at the end of the procedure (when performed).24 hours

Duration of the entire procedure, the additional procedure (BOOST), and the final ultrasound acquisition at the end of the procedure (when performed)

(For the last 5 patients): Estimate the quality of the registration after insertion of the implants.24 hours

(For the last 5 patients): Final ultrasound acquisition performed at the end of the procedure with the Trinity® Perine system

Assess toxicity (pre brachytherapy visit, M1, M3, M6, M12), with questionnaires12 months

Assessment of toxicity by questionnaires (IPSS score + urinary symptom quality of life).

IPSS:: International Prostate Score Symptom (0 to 35: Score 20-35: severely symptomatic. Score 8-19: moderately symptomatic)

Dose to CTV-dosi at 150%1 month

V150% \> 95% for CTV-dosi (on Variseed dosimetry) at J0

Trial Locations

Locations (1)

Isabelle Boudry

🇫🇷

Grenoble, France

© Copyright 2025. All Rights Reserved by MedPath