Phase
Condition
Prostate Cancer
Prostate Cancer, Early, Recurrent
Urologic Cancer
Treatment
HDR partial prostate brachytherapy
Clinical Study ID
Ages > 45 Male
Study Summary
Eligibility Criteria
Inclusion
Inclusion Criteria:
Age >45 and Life expectancy >10 years
Previous External Beam Radiotherapy (EBRT) dose up to 78Gray/39 fractions, 81Gray/45 fractions or 70 Gray/28 fractions or LDR brachytherapy with site ofrecurrence in an under-dosed or untreated site
> 3 year interval since EBRT
No late toxicity from prior EBRT > grade 2
Rising PSA post EBRT > nadir + 2 ng/ml but < 10 ng/ml
PSA Doubling time > 6 months
Negative staging with CT scan of the abdomen/pelvis and bone scan
Able to undergo multiparametric MRI with endorectal coil
Radiographic evidence of dominant intraprostatic lesion (DIL) as only area ofrecurrence (i.e unifocal recurrence) and corresponding to site of original disease
Biopsy confirmation of DIL with pathology review by British Columbia Cancer AgencyGenitoUrinary pathologist (TB)
Willing to provide informed consent
History and physical examination within 90 days of registration
ECOG performance status 0-1 prior to registration
IPSS < 16, or adequate voiding study (post void residual < 100cc and peak flow rate > 10 cc/second).
No prior trans urethral prostatic resection
Recurrence suitable for implant with HDR brachytherapy as assessed on ultrasoundsimulation (maximum PTV ideally < 65% of prostate volume)
No history of inflammatory bowel disease or previous rectal surgery
Suitable for procedure under anesthesia, spinal or general
INR <2.5 and platelet count >75 x 109/L
Androgen Deprivation Therapy may be initiated at the discretion of the treatingoncologist
Exclusion
Exclusion Criteria:
Not compliant with criteria above
Unable to give informed consent
Study Design
Study Description
Connect with a study center
BCCA Center for the Southern Interior
Kelowna, British Columbia V1Y 5L3
CanadaActive - Recruiting

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