This trial is active, not recruiting.

Condition recurrent prostate cancer
Treatment high intensity focused ultrasound
Sponsor SonaCare Medical
Start date July 2008
End date December 2016
Trial size 117 participants
Trial identifier NCT00772317, FSI-003


For the treatment of locally recurrent prostate cancer following failed external beam radiation therapy (EBRT)

United States No locations recruiting
Other Countries No locations recruiting

Study Design

Endpoint classification safety/efficacy study
Intervention model single group assignment
Masking open label
Primary purpose treatment
High Intensity Focused Ultrasound
high intensity focused ultrasound Sonablate 450
High Intensity Focused Ultrasound

Primary Outcomes

absence of biochemical failure, defined as achieving a PSA nadir of ≤ 0.5 ng/mL within 12 months of treatment
time frame: 12 months post treatment

Secondary Outcomes

negative prostate biopsy at the 12 month time point
time frame: 12 months post treatment

Eligibility Criteria

Male participants from 40 years up to 85 years old.

Inclusion Criteria: - subjects with initial presentation of organ confined recurrent prostate cancer (Stages T1c and T2 only) who have been treated with EBRT (conventional, 3D conformal, or IMRT) or proton therapy, two or more years prior, and currently have biopsy proven local recurrence. Previous radiation therapy must be a documented therapeutic dose of 60 to 81Gy or GyE (gray equivalent) for proton therapy; - Negative bone scan within 6 months prior to enrollment to rule out possibility of metastases; - Negative CT scans of the chest, abdomen, and pelvis within 6 months prior to enrollment to rule out possibility of metastases; - age ≥40 years through ≤85 years of age; - prostate biopsy with ≥10 core biopsies demonstrating 1 or more cores positive for cancer cells, within 6 months prior to treatment; - prostate volume ≤ 40 gms(cc) (HIFU subject prostate volume will be initially calculated utilizing TRUS measurements during screening and verified with the use of the Sonablate before initiating the HIFU procedure. Patients with prostate volumes greater than 40 gm(cc) as determined by either measurement will not be enrolled in the study); - AP diameter of the prostate must be ≤4.0cm; - serum prostate specific antigen (PSA) ≥0.5 ng/mL and ≤10 ng/mL; - >90 days post hormone therapy usages, subjects who have or are currently undergoing hormone therapy (GnRH agonist/antagonist) must discontinue hormone therapy and go through a 90 day washout period prior to consideration for study participation, and must remain off hormone therapy throughout the duration of the follow-up period (5 years); - signed informed consent for the HIFU treatment study through the 12 month follow-up visit (7 visits) and then through the extended follow-up period of 5 years (4 additional visits); - life expectancy > 12 months. Exclusion Criteria: - American Society of Anesthesiologists (ASA) criteria of IV or higher; - intra-prostatic calcifications >1.0 cm (single or continuous grouping) on 2 or more consecutive images along the same plane by either the TRUS or Sonablate 500 measurement will not be enrolled; - active, uncorrected bleeding disorder as determined by abnormal prothrombin time, partial thromboplastin time, or INR at the time of HIFU (use international lab normal ranges for parameters); - use of coumadin or any other anticoagulant, unless anticoagulation can be temporarily reversed or stopped; - active urinary tract infection; - interest in future fertility; - body weight which would preclude proper suprapubic catheter functioning, per investigator's discretion - inability to visualize the prostatic tissue adequately on transrectal ultrasound imaging; - use of any 5ARI drugs within 3 months prior to enrollment such as Finasteride (Proscar) or Dutasteride (Avodart); - a debulking transurethral resection of the prostate (TURP) is not acceptable once the screening biopsy for patient selection has been conducted; - prior treatment for prostate cancer, other than EBRT or hormone therapy; - history of urethral stent or urethral surgery (urethral dilation, urethroplasty); a Uroflow exam may be conducted at the investigators discretion; - prior significant rectal surgery (hemorrhoidectomy is acceptable; rectal resection/fissure repair are excluded); - history of inflammatory bowel disease of the rectum; - history of any other malignancy treated within the last 5 years, other than squamous or basal cell skin cancer; - functional bladder problems defined as IPSS > 19; - current bladder cancer, urethral stricture, or bladder neck contracture; a cystoscopy my be performed at the investigator's discretion to rule out these conditions; - urinary tract or rectal fistula; - rectal fibrosis/stenosis; anoscopy or proctoscopy may be performed at the investigator's discretion; - anomaly of the rectal anatomy or mucus membrane; anoscopy or proctoscopy may be performed at the investigator's discretion; - prostate seroma/abscess; - current symptomatic radiation proctitis requiring creams; - participation in other investigational studies, unless approved in writing by the study sponsor.

Additional Information

Official title A Multicenter Clinical Study of the Sonablate® 450 (Sonablate) for the TreAtment of Locally Recurrent Prostate Cancer With HIFU (STAR Trial)
Description The proposed study is a non-randomized, prospective, single arm study. The safety and effectiveness of the Sonablate treatment in subjects with locally recurrent prostate cancer will be evaluated with regard to freedom from biochemical failure and disease recurrence following HIFU treatment. Men with histologically confirmed, locally recurrent, organ-confined, non-metastatic prostatic adenocarcinoma two or more years following EBRT, PSA ≥0.5 ng/mL and ≤10 ng/mL, 40 to 85 years of age, and with initial staging of T1c-T2 prior to radiation, who meet the criteria for salvage treatment, will be enrolled. This pivotal study will cover pre-treatment through the 12-month post-treatment follow-up visit (8 visits). A 5 year extended follow-up study will be conducted annually for the 2nd-5th years post treatment (4 additional visits).
Trial information was received from ClinicalTrials.gov and was last updated in January 2016.
Information provided to ClinicalTrials.gov by SonaCare Medical.
Location data was received from the National Cancer Institute and was last updated in April 2016.