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An Evidence-Based Focal Cryotherapy Protocol for Focal Ablation of Intermediate Risk Prostate Cancer

Status: Recruiting
Location: See location...
Intervention Type: Other, Drug
Study Type: Interventional
Study Phase: Phase 2
SUMMARY

To learn if using cryotherapy to treat only the part of the prostate known to contain cancer is effective in controlling prostate cancer

Eligibility
Participation Requirements
Sex: Male
Minimum Age: 18
Healthy Volunteers: f
View:

• English-speaking adult males

• Life expectancy over 10 years as assessed by treating physician

• Prior to enrollment, MRI fusion biopsy of MRI-visible lesion required (as detailed below, which includes systematic biopsy cores)

• 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)

‣ Histologically confirmed adenocarcinoma of prostate

⁃ Organ-confined prostate cancer, clinical stage ≤T2bN0M0

⁃ Visible tumor on MRI

⁃ No clear evidence or high suspicion of extraprostatic extension or seminal vesical invasion on MRI

⁃ 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).

⁃ 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.

⁃ 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

• Physician can fully visualize the prostate on transrectal ultrasound on entry biopsy

• Lesion anatomically amenable to cryotherapy treatment based on treating physician's discretion

• Willing and able to read, understand and sign the study specific informed consent document

• Willing and agreeable to comply with study protocol requirements, including focal cryotherapy ablation and all follow up visit requirements

• Patients must consent to investigative laboratory protocol (such as, but not limited to, 2021- 0560)

Locations
United States
Texas
MD Anderson Cancer Center
RECRUITING
Houston
Contact Information
Primary
Justin Gregg, MD
jrgregg@mdanderson.org
713-792-3250
Time Frame
Start Date: 2022-07-25
Estimated Completion Date: 2028-01-31
Participants
Target number of participants: 30
Treatments
Experimental: Focal therapy Treatment
Cryoablation is a procedure in which special needles are inserted into the tumor site.
Related Therapeutic Areas
Sponsors
Leads: M.D. Anderson Cancer Center

This content was sourced from clinicaltrials.gov

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