Improving Assessment (and Ultimately Outcomes) of Permanent Prostate Implant Therapy
This study addresses three major sources of post-implant dosimetry inaccuracy for permanent
prostate implants: post-operative edema, prostate contour delineation, and dose calculation
method. It is hypothesized that a pragmatic edema model can minimize the first
uncertainty, co-registered CT + MR images the second, and an improved dose calculation
algorithm the third.
Detailed objectives are to:
- measure and model the effects of edema on dosimetry;
- evaluate CT + MR image registration methods;
- compare dosimetry for CT alone vs. CT + MRI using the contemporary TG-43 dose
calculation method;
- set up a Monte Carlo code that makes full use of the information in CT + MR images to
perform implant dose calculations;
- compare prostate dosimetry for the Monte Carlo vs. the simpler TG-43 method;
- develop an analytical post-implant dose calculation algorithm for routine clinical use
(Monte Carlo is too slow on a single-CPU brachytherapy planning computer); and finally
- assess the performance of the new algorithm.
Of the estimated 250,000 new cases of prostate cancer in North America in 2004, most are
early stage disease as a consequence of PSA testing. Permanent prostate implant therapy is
a major option for this group, as long-term clinical studies indicate a cure rate equal to
surgery and external beam radiotherapy, but with fewer complications. By dealing with
dosimetric inaccuracies, a proven treatment can reach its full potential.
Interventional
Endpoint Classification: Efficacy Study, Intervention Model: Single Group Assignment, Masking: Open Label, Primary Purpose: Treatment
implant dose coverage at 4 weeks, comparing CT and MRI versus CT alone
Ron Sloboda, PhD
Principal Investigator
Alberta Health Services
Canada: Health Canada
SP-14-0044 / 21694
NCT00127816
April 2005
December 2012
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