30 patients (median age 74 years) were enrolled in the study. Median follow up from salvage HDR was 33 months (12-60). At initial presentation, there were 3, 18 and 9 low-, intermediate- and high-risk disease. The initial XRT dose was 70-78Gy with conventional fractionation in 28 patients and alternate fractionation in 2 patients (35Gy/5F and 50Gy/15F). The Gleason score of the local recurrence was 6, 7 and 8-10 in 2, 19 and 9, respectively. The pre-HDR median PSA was 3.67ng/mL (0.63–11.01). The median of the prostate was 33.8 mL (15.9-86.0) and TV was 4.7mL (1.5-15.5). The median dosimetric endpoints per implant were: prostate V10.5Gy 96.5% (94.1-98.7), prostate D90 11.4Gy (10.9-12.0), TV V13.5Gy 94.2% (63.3-100), TV D90 18.1Gy (15.0-22.2), urethral D10% 12.0Gy (11.5-12.6), urethral Dmax 12.6Gy (12.2-13.5) and rectal V8.4Gy 0mL (0-0.8). Four patients (13%) required temporary urinary catheterization. There were no acute/late GU/GI grade 3-5 toxicities. The most common acute toxicity was frequency, dysuria and urgency. Mean IPSS at baseline, 1.5-, 3-, 6-, 9-, 12-, 18-, 24-, 30- and 36-months was 6, 15, 10, 11, 10, 12, 10, 10, 9 and 7, respectively (p=0.03). Three-year PSA progression-free survival and freedom from ADT rate was 67% and 93%, respectively. Of the 26 patients who had a post-HDR MRI (median 415 days), 18 (69%) patients had a complete response and 8 had persistent disease in the TV. No patients recurred elsewhere in the prostate.