A Multicenter Clinical Study of the Sonablate®450 for the TreAtment of Locally Recurrent Prostate Cancer With HIFU (STAR Trial)
Basic Trial Information
|No phase specified||Treatment||Active||40 to 80||Other||FSI-003|
For the treatment of locally recurrent prostate cancer following failed external beam radiation therapy (EBRT)
Further Study Information
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).
- 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.
- 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.
Trial Contact Information
Trial Lead Organizations/Sponsors
High Intensity Focused Ultrasound
District of Columbia
Walter Reed National Military Medical Center
Judith Travis, CCRC
COL. David G. McLeod, M.C., M.D.
Link to the current ClinicalTrials.gov record.
NLM Identifier NCT00772317
ClinicalTrials.gov processed this data on April 14, 2015
Note: Information about this trial is from the ClinicalTrials.gov database. The versions designated for health professionals and patients contain the same text. Minor changes may be made to the ClinicalTrials.gov record to standardize the names of study sponsors, sites, and contacts. Cancer.gov only lists sites that are recruiting patients for active trials, whereas ClinicalTrials.gov lists all sites for all trials. Questions and comments regarding the presented information should be directed to ClinicalTrials.gov.