Spots Global Cancer Trial Database for MRI/Ultrasound Fusion Guided Prostate Cryotherapy

Study Description

Brief Summary: Registration of Prostate Cancer patients undergoing Prostate Cryotherapy guided by Mutiparametric-MRI (MP-MRI) highlighting biopsy confirmed regions. The primary outcome measure is 5 year oncological control. Secondary aim is lack of progression beyond the prostate gland. The aim of intervention is to eradicate prostate cancer disease in the treated area while imposing no or minimal deleterious effects in quality of life.

Detailed Description: CLINICAL TRIAL OF OBSERVATION NATURE PRIMARY OUTCOME Cancer control of treated areas 5, 10, 15 years after intervention based on prostate biopsy of initial treated area, progression requiring conversion to radical prostate surgery or radiation or other forms of whole gland treatment (ej, HIFU), Metastatic Free survival: CT Scan and Bone Scans, Cancer-Specific and Overall Survival SECONDARY OUTCOMES Secondary Interventions focal interventions due to de-novo lesions. Focal or target therapy rescue with other technologies (ej HIFU); Short, Intermediate and Long-Term Urinary and Sexual Function changes in quality of life measured by validated inventories; Anxiety related to cancer and cancer control. Treatment tolerance to local anesthesia. Patient App compliance and activity to monitor care DATA COLLECTION * Complete H\&P, family history, past medical and surgical history, social history, allergies, and medications * As of July 2016, voluntary measurement thru Focalyx App for smartphones and tablets * Imaging Specifics Assessing Prostate, Seminal Vesicles and Urethral Contouring by Multi-parametric-MRI. Dominant lesions and secondary lesions contouring my MP-MRI. * Procedure specific Co-Registration quality with ultrasound denoting quality * Specific ablative description and digitalization of critical measures such as: ablation type (ej cryotherapy, equipment used) procedure, cryoprobes used, freeze/thaw cycles timing, temperatures at neurovascular bundles, denonvilliers fascia. Urethral warmer requirements * Follow up information: 30 day perioperative outcomes (incidence of UTI, urinary retention, failure of local anesthetic, pain measures). 6 week, 3,6,9,12 month and then every 6 month measures of PSA, Testosterone levels, Urinary Function and Sexual Function inventories, Overall anxiety and regret related to diagnosis and treatment * Uroflow and PVR measurements by 3 to 6 month of treatment * MP MRI on a yearly basis, for years 2,3,4 after treatment, biopsy driven by new suspicious MRI findings * MP MRI triggered by elevation in PSA velocity or PSA level 10% above diagnosis * Transperineal Fusion Guided Prostate biopsy at 1st year - emphasis on treated areas, suspicious MRI areas * Transperineal Fusion Guided Prostate biopsy at 5th year - emphasis on treated areas, suspicious MRI areas * 5, 10, 15 Yr CT Scans, PET Scan/Bone Scan SAFETY MEASURES * Periodic evaluation of registry to ensure consistency in follow up * Patient remainders of tests required

Keywords

Eligibility

Minimum Age: 55 Years

Eligible Ages: ADULT, OLDER_ADULT

Sex: MALE

Healthy Volunteers: No

Locations

Contact Details

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