An Evidence-Based Focal Cryotherapy Protocol for Focal Ablation of Intermediate Risk Prostate Cancer
Study Details
Study Description
Brief Summary
To learn if using cryotherapy to treat only the part of the prostate known to contain cancer is effective in controlling prostate cancer
| Condition or Disease | Intervention/Treatment | Phase |
|---|---|---|
|
Phase 2 |
Detailed Description
Primary Objective:
• To determine the effectiveness of an evidence-based focal cryotherapy ablation by measuring negative in-field recurrence rate at 6-months post-ablation.
Secondary Objectives:
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To determine quality of life following focal prostate cancer ablation using validated questionnaires (EPIC-26, AUA symptoms score, SHIM).
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To establish PSA kinetics post-evidence-based focal cryotherapy ablation.
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To determine rates of out of field recurrence on 6-month biopsy following focal cryotherapy ablation.
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To determine MRI findings post-focal cryotherapy ablation, including those related to prostate and surrounding periprostatic fat volume.
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To determine rate of progression and re-intervention collected as part of standard of care treatment for 5-year following study treatment.
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To describe financial toxicity associated with focal prostate cancer treatment using cryotherapy.
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To describe the incidence and severity of complications within 30-days after the study focal ablation treatment.
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To describe imaging findings on PSMA PET MRI performed in a subset of men after standard of care focal cryotherapy prior to 6-month biopsy.
Study Design
Arms and Interventions
| Arm | Intervention/Treatment |
|---|---|
| Experimental: Focal therapy Treatment Cryoablation is a procedure in which special needles are inserted into the tumor site. |
Other: Focal Cryoablation
Participants will have the Focal cryoablation placed by the needles in such a way that the area of affected tissue is much smaller and focus just on the tumor tissue and surrounding area
Other: Standard of Care
Participants will receive a prostate biopsy.
Other: Quality-of-life Questionnaires
Participants will fill out questionnaires.
|
Outcome Measures
Primary Outcome Measures
- Quality-of-life Questionnaires [through completion an average of 1 year.]
Score scale ranges (0-5) 0-Not at all/5- Almost always
Eligibility Criteria
Criteria
Inclusion criteria:
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English-speaking adult males
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Life expectancy over 10 years as assessed by treating physician
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Prior to enrollment, MRI fusion biopsy of MRI-visible lesion required (as detailed below, which includes systematic biopsy cores)
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Single focus GG2 or GG3 (additional GG1 allowed up to 6mm, noting that a single focus of disease is defined as an area seen on MRI that may be biopsied multiple times using targeted biopsies and have systematic core biopsies directly adjacent to targeted cores; all of which being considered as from the same focus)
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Histologically confirmed adenocarcinoma of prostate
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Organ-confined prostate cancer, clinical stage ≤T2bN0M0
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Visible tumor on MRI
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No clear evidence or high suspicion of extraprostatic extension or seminal vesical invasion on MRI
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Biopsy via transperineal or transrectal approach with at least 2 cores of MRI visible lesions that are PIRADS 2 or higher and 12 core systematic biopsy template (exclusion of cores from systematic template that overlap with targeted cores allowed).
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Additional performance of microultrasound guided biopsy is allowed though not required. Please note that every effort will be made to correlate microultrasound findings with MRI, in order to determine if positive results are from the same MRIvisible focus. This determination will be made by the surgeon performing the biopsy.
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Note that GGG 1 disease at sites other than ablation zone are allowed provided these are 6mm or less in size. PSA ≤15 ng/mL, or PSAD <0.15 if PSA >15 ng/mL
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Physician can fully visualize the prostate on transrectal ultrasound on entry biopsy
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Lesion anatomically amenable to cryotherapy treatment based on treating physician's discretion
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Willing and able to read, understand and sign the study specific informed consent document
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Willing and agreeable to comply with study protocol requirements, including focal cryotherapy ablation and all follow up visit requirements
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Patients must consent to investigative laboratory protocol (such as, but not limited to, 2021- 0560)
Exclusion criteria:
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Gleason grade group 4 or 5 disease
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Medical history or concurrent disease, which in the opinion of the investigator, poses the patient at significant peri-operative risk of complication due to anesthesia or the procedure
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Active urinary tract infection
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Any previous treatment for prostate cancer, including radiation therapy, hormonal treatment, biologic therapy for prostate cancer, or chemotherapy
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Prior TURP or other prostate outlet procedure such as HoLEP, greenlight, microwave ablation, aquablation, UroLift, or simple prostatectomy.
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Previous rectal surgery (other than hemorrhoidectomy) or history of rectal disease
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Inability to obtain prostate MRI (ex. due to claustrophobia, pacemaker, or prohibitive implants)
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Unwilling to consent to laboratory investigative protocol (such as, but not limited to, 2021- 0560)
Contacts and Locations
Locations
| Site | City | State | Country | Postal Code | |
|---|---|---|---|---|---|
| 1 | MD Anderson Cancer Center | Houston | Texas | United States | 77030 |
Sponsors and Collaborators
- M.D. Anderson Cancer Center
- Philanthropic Sources
Investigators
- Principal Investigator: Justin Gregg, MD, jrgregg@mdanderson.org
Study Documents (Full-Text)
None provided.More Information
Additional Information:
Publications
None provided.- 2022-0165
- NCI-2022-05462