Prostate Cancer Clinical Trial
Official title:
Phase II Study of Focused Dose Painted I-125 Brachytherapy for Low to Intermediate Risk Prostate Cancer Using Deformable Registration of Multi-parametric MRI (Magnetic Resonance Imaging) to Intra-operative TRUS (Trans Rectal Ultrasound)
Objective:
To focus the high dose radiation to the gross tumor in the prostate while maintaining
adequate dose for control of microscopic disease elsewhere in the prostate.
In order to test the incorporation of the robust MRI and TRUS fusion algorithm in the
clinical setting the investigators planned a study of Focused therapy with a primary
endpoint of accurate localization of the high risk region. This is a pilot study of dose
painted permanent I-125 seed implant to verify absence of tumor cells outside a high risk
region using multi-parametric MRI and deformable TRUS registration. The high risk region
will be dose painted to 160 Gy and the rest of the prostate will receive the normal
prescription dose.
Primary end-point:
Feasibility of dose painting will be determined by the absence of tumor outside the
high-risk region on an intra-operative trans-perineal biopsy.
Frozen sections will not be obtained, however on receipt of the final pathology 2-4 weeks
after the procedure 2 possible scenarios arise:
1. There is no evidence of cancer: this confirms the accuracy of the TRUS MRI
registration.
2. There is evidence of tumor on the stereotactic biopsy: In this case a regular
dosimetric check (this is performed in the Standard of care procedure and is known as
post-operative dosimetry) will be performed to determine whether adequate dose was
delivered. If not, as the involved needle position was recorded in the treatment plan
and labeled with co-ordinates, the regular possibility of accurately adding radioactive
seeds is possible.
;
Observational Model: Case-Only, Time Perspective: Prospective
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