Unilateral Nerve-Sparing Cryoablation for Low-Risk, Clinically Localized, Unilateral Prostate Cancer (POTENT-C)

NYU Langone Health

Status and phase

Terminated

Phase 2

Conditions

Prostate Cancer

Treatments

Device: Precise Cryoablation System with IceRod Needles

Procedure: Unilateral Nerve-Sparing Cryoablation of the Prostate

Study type

Interventional

Funder types

Other

Identifiers

NCT02459912

15009

Details and patient eligibility

About

Men with low-risk, clinically localized, unilateral prostate cancer will be treated with unilateral nerve-sparing cryoablation and evaluated for the rate of potency, cancer control and health related quality of life outcomes after treatment.

Full description

This study is a clinical trial to determine and assess the change in the rate of potency in men with low-risk, localized, unilateral prostate cancer who have not received previous treatment. A total of 86 men between 40 to 69 years of age with biopsy proven, early stage localized prostate cancer will receive unilateral nerve-sparing cryoablation. The study includes a screening/pre-operative visit, a cryoablation procedure day, and 10 follow up visits over the course of 36 months. The first follow-up visit will occur within 2 weeks (±1 week) after cryoablation. Thereafter, follow-up visits will be scheduled, from the date of procedure, every 3 months (±3 weeks) for 18 months and every 6 months (±3 weeks) thereafter until the patient completes the protocol, 36 months after the cryoablation procedure.

Enrollment

1 patient

Sex

Male

Ages

40 to 69 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

Life expectancy >5 years
Willing and able to freely sign informed consent to enroll in the study
Willing to complete sexual function and HRQoL questionnaires
Sexually active and potent (able to achieve an EPIC questionnaire sexual domain score greater than or equal to 75 without the use of any devices or medicines to enhance erections)
Prostate gland volume greater than or equal to 20cc and less than or equal to 60cc
Does not have stress urinary incontinence defined as urinary leakage requiring the use of any protective pads
Most recent serum PSA <10 ng/mL taken at least 6 weeks after a previous biopsy and 3 months +/- 2 weeks prior to study cryoablation
Histologically proven, clinical stage T1c-T2b prostate cancer in the proposed treated side
Untreated contralateral side has no malignant elements demonstrated by biopsy
Patient does not have ASAP (Atypical Small Acinar Proliferation) in the untreated side
Patient has documented, biopsy proven unilateral disease (via a minimum of 6 biopsy cores taken on the cancerous side and a minimum of 12 negative cores on the non-cancerous side) using transrectal ultrasound (TRUS) guidance
A 12 core biopsy using transrectal ultrasound (TRUS) guidance taken within 3 months prior to enrollment from the non-cancerous side and each core was biopsied by a site investigator
Biopsied areas in the non-cancerous side include the following zones: L/R (left or right side) lateral base, L/R mid gland base, L/R medial base, L/R lateral middle, L/R mid gland middle, L/R medial middle, L/R lateral apex, L/R mid gland apex, L/R medial apex, L/R transitional base, L/R transitional mid, L/R anterior horn
Prostate biopsy Gleason Score (GS) is less than or equal to 7. Gleason Score 3+4=7 [but not 4+3=7] is allowed as long as the score is based upon no more than 2 cores with cancer involvement of 50% or less.
Does not have a biopsy GS 3+4=7 combined with clinical stage T2b
Either a nodule was not felt (T1c) OR the palpable nodule (T2a or T2b) is on the same side as the positive biopsy

Exclusion criteria

Previous treatment for prostate cancer including radiation, cryoablation, chemotherapy, surgery, high intensity focused ultrasound, and/or hormone therapy
Previous invasive or minimally invasive treatment for benign prostatic hypertrophy (BPH) (i.e., TURP, TUMPT, WIT, TUNA)
Inability to tolerate a transrectal ultrasound
Active urinary tract infection
Evidence of metastatic disease
Irreversible bleeding diathesis or other bleeding disorders
Anatomic penile abnormalities precluding cryoablation
Erectile dysfunction (EPIC Questionnaire sexual domain score <60) at baseline, including the use of any erectile aid (PDE-5, etc) to increase the EPIC Questionnaire (Appendix D) sexual domain score >75, without which the patient would not qualify for the study
Current or history within the past 6 months of alcohol and/or substance abuse which would impair participation in the study
Major medical disorder (i.e. uncontrolled diabetes, significant hepatic, renal, or hematological disorders, recent stroke or myocardial infarction), in the opinion of the urologist, is an illness or complication which is not consistent with the protocol requirements
Unwilling to undergo the necessary follow-up for the trial period
Bilateral prostate cancer disease
Significant median lobe of the prostate which would preclude an adequate cryoablation procedure (based on the discretion of the urologist)
Uncontrolled intercurrent illness including, but not limited to, ongoing or active infection, symptomatic congestive heart failure, unstable angina pectoris, cardiac arrythmia, or psychiatric illness/social situations which would limit compliance with study requirements
Known HIV or AIDS-related illness