Primary Malignant Neoplasm of Prostate (Diagnosis)
Conditions
Brief summary
The purpose of this research is to collect data about the MRI cryoablation procedure your doctor(s) would normally perform in order to treat the participants focal prostate cancer and to evaluate the participants condition after the participants treatment is performed. Participants have been asked to take part in this research because the participants have been diagnosed with prostate cancer and scheduled to have an ablation procedure.
Detailed description
The purpose of this study is to evaluate MR-guided cryoablation of biopsy proven prostate tumors using the Galil MRI-compatible cryoablation system. The system has been approved by the United States Food and Drug Administration (FDA) for soft tissue ablation and has been utilized successfully at Mayo. All procedures will be performed according to approved indications. the investigators wish to monitor the technique and collect data at the participants follow-up visits. The study only collects data about the MRI-guided cryoablation procedure the participants doctor(s) would normally perform in order to treat the participants focal prostate cancer and to evaluate the participants condition after there treatment is performed. The participants doctor will advise the participants when the participants should return for follow-up visits. These visits will be according to the participants doctor's standard of care; usually return visits are at 3-6months, 12 months, 24 months, 36 months, 48 months and 60 months after the procedure, although the participants doctor may ask that the participants return for more frequent visits.
Interventions
PROCEDUREMR guided cryoablation
MR guided cryoablation of focal biopsy proven prostate cancer
Sponsors
Mayo Clinic
Study design
Observational model
COHORT
Time perspective
PROSPECTIVE
Eligibility
Sex/Gender
MALE
Age
30 Years to 100 Years
Healthy volunteers
No
Inclusion criteria
* Patients with "biopsy proven" Gleason7 prostate cancer referred to Urology and/or Interventional Radiology for treatment * Surgery and/or Radiation is not a desirable alternative therapy at the time of enrollment * Tumor size is \< 2 cm at its largest diameter * Tumor does not encompass the rectal wall or external urethral sphincter * Patient is able to undergo MRI
Exclusion criteria
•
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| Technical success of the MR-guided cryoablation | Will assess for 5 years with interval assessment each year | Determine the technical success of the MR-guided cryoablation as measured by complete target lesion ablation. |
| Safety of the MR-guided cryoablation | Will assess for 5 years with interval assessment each year | Determine safety of the MR-guided cryoablation using continuous MR imaging during the procedure. |
| Examine short term tumor recurrence | Will assess for 5 years with interval assessment each year | Examine short term tumor recurrence over 6 months with contrast enhanced MRI and as required MR or U/S guided biopsy of prostate bed if PSA biochemical recurrence. |
Secondary
| Measure | Time frame | Description |
|---|---|---|
| MR procedure time. | Will assess for 5 years with interval assessment each year | We will examine the time for each step in the process to create a stream-lined process and minimize MR procedure time. |
Countries
United States
Contacts
CONTACTDesirae Howe-Clayton
Outcome results
None listed