Recurrent Prostate Cancer
Conditions
Keywords
prostate cancer, magnetic resonance imaging, guided imagery
Brief summary
In this study we will test a new procedure to guide needle biopsies into the prostate gland based on MRI. This study will be conducted in patients who may have recurrence of their cancer in the prostate gland after radiation therapy in order to map out the location of the recurrence. Using this technique, we will be able to measure the accuracy of MR images in identifying the site of tumour recurrence.
Detailed description
This study involves the technical development and clinical testing of a novel technique for magnetic resonance imaging (MRI) guided prostate biopsy in a 1.5T horizontal bore scanner using a dedicated interventional table. We primarily hypothesize that the integration of diagnostic and interventional MRI enables needle biopsy targeting to foci of tumor recurrence after radiotherapy, and will enable a determination of the diagnostic accuracy of MRI in mapping sub-sites of tumor recurrence after radiotherapy. RELEVANCE TO PUBLIC HEALTH: Patients with recurrence of their prostate cancer after radiotherapy currently face difficult choices. Standard second line treatments target the entire prostate gland and are associated many side effects. This study will directly improve the detection, spatial delineation, and characterization of prostate cancer persistence after radiotherapy. If anatomic patterns of disease persistence are found across patients, radiation delivery techniques will be suitably modified, which may translate to improved cure rates. Importantly, this study will establish a procedural platform for MRI-guidance of minimally invasive local salvage therapies. By precisely focusing salvage therapy to sites of tumor persistence within the prostate gland, side effects may be reduced in the future.
Interventions
PROCEDUREMRI-Guided Biopsy
Technical development and clinical testing of a novel technique for magnetic resonance imaging (MRI) guided prostate biopsy in a 1.5T horizontal bore scanner using a dedicated interventional table.
Sponsors
U.S. Army Medical Research and Development Command
Princess Margaret Hospital, Canada
University Health Network, Toronto
Study design
Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
DIAGNOSTIC
Masking
NONE
Eligibility
Sex/Gender
MALE
Age
18 Years to No maximum
Healthy volunteers
No
Inclusion criteria
* Biochemical failure \> 18 months after definitive external beam radiotherapy (ASTRO definition - revised version 2006: rise by 2 ng/mL or more above the nadir PSA) * PSA \<20 prior to initial course of external beam radiotherapy * PSADT \>3 months at failure * Age ≥ 18 years * ECOG performance status 0 or 1 with \>10 year life expectancy * Fit for local anaesthesia * Informed consent:
Exclusion criteria
* Contraindications to MRI * Severe claustrophobia * Bleeding diathesis and anti-coagulative therapy that cannot be temporarily ceased precluding brachytherapy * Previous brachytherapy * Active hormonal therapy * Radiologic evidence of LN or distant metastases * Other urinary or medical conditions deemed by the PI or associates to make the patient ineligible for MRI-guided prostate biopsy. * Contraindications to endorectal coil, surgically absent rectum, severe hemorrhoids or previous colorectal surgery * Contraindications to conscious sedation * Contraindication to IV Gadolinium administration * latex allergy
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| The primary endpoint is a preliminary estimate of the diagnostic accuracy of MRI in identifying sites of recurrent tumor after radiotherapy for prostate cancer. | at the end of the evaluation phase |
Countries
Canada
Outcome results
None listed