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Deformable Registration of Multi-parametric MRI to Intra-operative Transrectal Ultrasound for Prostate Brachytherapy

Phase II Study of Focused Dose Painted I-125 Brachytherapy for Low to Intermediate Risk Prostate Cancer Using Deformable Registration of Multi-parametric MRI (Magnetic Resonance Imaging) to Intra-operative TRUS (Trans Rectal Ultrasound)

Status
UNKNOWN
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT02790216
Enrollment
24
Registered
2016-06-03
Start date
2016-06-30
Completion date
2020-06-30
Last updated
2016-06-03

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

Conditions

Prostate Cancer

Keywords

Image guided brachytherapy

Brief summary

Objective: To focus the high dose radiation to the gross tumor in the prostate while maintaining adequate dose for control of microscopic disease elsewhere in the prostate. In order to test the incorporation of the robust MRI and TRUS fusion algorithm in the clinical setting the investigators planned a study of Focused therapy with a primary endpoint of accurate localization of the high risk region. This is a pilot study of dose painted permanent I-125 seed implant to verify absence of tumor cells outside a high risk region using multi-parametric MRI and deformable TRUS registration. The high risk region will be dose painted to 160 Gy and the rest of the prostate will receive the normal prescription dose.

Detailed description

Primary end-point: Feasibility of dose painting will be determined by the absence of tumor outside the high-risk region on an intra-operative trans-perineal biopsy. Frozen sections will not be obtained, however on receipt of the final pathology 2-4 weeks after the procedure 2 possible scenarios arise: 1. There is no evidence of cancer: this confirms the accuracy of the TRUS MRI registration. 2. There is evidence of tumor on the stereotactic biopsy: In this case a regular dosimetric check (this is performed in the Standard of care procedure and is known as post-operative dosimetry) will be performed to determine whether adequate dose was delivered. If not, as the involved needle position was recorded in the treatment plan and labeled with co-ordinates, the regular possibility of accurately adding radioactive seeds is possible.

Interventions

PROCEDUREBrachytherapy

Biopsies will be obtained after intraoperative plan to rule out significant cancer outside a high risk planning target volume

Sponsors

Sheba Medical Center
Lead SponsorOTHER_GOV

Study design

Observational model
CASE_ONLY
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
MALE
Age
50 Years to 90 Years
Healthy volunteers
No

Inclusion criteria

* Men suitable for monotherapy with permanent Iodine 125 implant * Age \> 50 yrs * PS 0-2 (WHO) * Histologic diagnosis of prostate adenocarcinoma made on transrectal guided prostate biopsy with no fewer than 12 cores taken * No more than 50% of cores involved (summary) * MRI of Prostate with Diffusion Weighted Imaging and Dynamic Contrast Enhancement with demonstrable lesion compatible with biopsy result * Gleason sum no greater than 3+4 =7 in any core * Clinical T stage no higher than T T (tumor) 2A * Prostate volume ≤60 cc * Serum prostate-specific antigen (PSA) no higher than 15 ng/mL * No prior history of malignancy except non-melanoma skin cancer * Must be suitable for general or spinal anesthesia

Exclusion criteria

Have anesthesia surgical assignment category IV or greater * Cannot cease anti-coagulant therapy * Had a malignancy, other than prostate or skin cancer (except malignant melanoma), within 5 years * urethral stricture * Prior prostate cancer therapies

Design outcomes

Primary

MeasureTime frameDescription
Percentage of patients with a positive biopsy outside the defined High risk Planning Target VolumePathological report due one month after brachytherapy implantNegative biopsy outside the high risk planning target volume will confirm the accuracy of the MRI TRUS elastic fusion algorithm to locate the tumor

Secondary

MeasureTime frameDescription
Biochemical failure as determined by Prostate specific antigen greater than nadir+2 ng/ml3 years
Urinary , Sexual ,Bowel and Vitality function domains6 months and then at years one , two and threeExpanded Prostate Inventory Composite (EPIC)

Countries

Israel

Contacts

Primary ContactZvi Symon, MD
symonz@sheba.health.gov.il97235308175

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026