Long-Term Outcomes of a Prospective Study on Magnetic Resonance Imaging-Guided Whole-Gland Salvage High-Dose-Rate Prostate Brachytherapy for Locally Recurrent Prostate Cancer
7 affiliations
- 1Department of Radiation Oncology, Sunnybrook Odette Cancer Centre, Toronto, Ontario, Canada
- 2Department of Radiation Oncology, University of Toronto, Toronto, Ontario, Canada
- 3Department of Oncology and Nuclear Medicine, Sestre Milosrdnice University Hospital Center, Zagreb, Croatia
- 4Croatian Catholic University School of Medicine, Zagreb, Croatia
- 5Department of Radiation Oncology, BC Cancer Kelowna, Kelowna, British Columbia, Canada
- 6Department of Medical Imaging, Sunnybrook Health Sciences Centre, Toronto, Ontario, Canada
- 7Department of Medical Imaging, University of Toronto, Toronto, Ontario, Canada
Abstract
Purpose: Whole-gland salvage high-dose-rate (HDR) prostate brachytherapy is an emerging option for radiorecurrent prostate cancer. However, long-term prospective data remain limited. This report presents the long-term results of our prospective study on the toxicities, health-related quality of life, and efficacy of whole-gland HDR prostate brachytherapy.
Methods and Materials: Patients with biopsy-confirmed, magnetic resonance (MR)-visible local recurrent prostate cancer after previous external beam radiation therapy (EBRT) were eligible. Patients underwent MR-assisted, ultrasound-based whole-gland HDR prostate brachytherapy with a prescription dose of 21 Gy to the entire prostate and 27 Gy to the MR-defined intraprostatic target volume (TV) divided over 2 implants separated by 1 to 2 weeks. Adjuvant androgen deprivation therapy was not used.
Results: Thirty patients were enrolled in the study. Median follow-up from salvage HDR was 72.0 months (10.7-121.5 months). Most patients (93%) had initial EBRT doses at conventional fractionation. The pre-HDR median prostate-specific antigen was 3.67 ng/mL (0.56-11.01 ng/mL). Seven (23.3%) were staged with prostate-specific membrane antigen positron emission tomography. Four (13%) required temporary urinary catheterization. There was only 1 (3.3%) grade 3 to 5 toxicity—a late grade 3 genitourinary toxicity. The prostate-specific antigen progression-free survival and freedom from androgen deprivation therapy rates were 73.0% and 93.0% at 3 years, and 24.8% and 69.6% at 5 years, respectively. Of the 26 patients who had a post-HDR MR imaging (median, 415 days), 9 (35%) had persistent disease. Of the 23 (77%) patients who had prostate-specific antigen relapse, 18 (78%) patients had disease at the TV confirmed by MR imaging, prostate-specific membrane antigen positron emission tomography, or targeted biopsy.
Conclusions: Whole-gland salvage HDR brachytherapy with intraprostatic boost is well tolerated. Progression after salvage treatment was associated with local failure.
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BibTeX
@article{hu2026longterm,
title = {{Long-Term Outcomes of a Prospective Study on Magnetic Resonance Imaging-Guided Whole-Gland Salvage High-Dose-Rate Prostate Brachytherapy for Locally Recurrent Prostate Cancer}},
author = {Hsin-Pei Hu and Gerard Morton and Andrew Loblaw and Chia-Lin Tseng and Jure Murgic and Ananth Ravi and Melanie Davidson and Matt Wronski and Moti Paudel and Masoom Haider and Andrea Deabreu and Liying Zhang and Hans T. Chung},
journal = {Advances in Radiation Oncology},
year = {2026},
month = aug,
doi = {10.1016/j.adro.2026.102168},
url = {https://doi.org/10.1016/j.adro.2026.102168},
note = {CC BY-NC-ND 4.0},
}
RIS
TY - JOUR
TI - Long-Term Outcomes of a Prospective Study on Magnetic Resonance Imaging-Guided Whole-Gland Salvage High-Dose-Rate Prostate Brachytherapy for Locally Recurrent Prostate Cancer
AU - Hsin-Pei Hu
AU - Gerard Morton
AU - Andrew Loblaw
AU - Chia-Lin Tseng
AU - Jure Murgic
AU - Ananth Ravi
AU - Melanie Davidson
AU - Matt Wronski
AU - Moti Paudel
AU - Masoom Haider
AU - Andrea Deabreu
AU - Liying Zhang
AU - Hans T. Chung
PY - 2026
DA - 2026/08/21
JO - Advances in Radiation Oncology
DO - 10.1016/j.adro.2026.102168
UR - https://doi.org/10.1016/j.adro.2026.102168
AB - Purpose: Whole-gland salvage high-dose-rate (HDR) prostate brachytherapy is an emerging option for radiorecurrent prostate cancer. However, long-term prospective data remain limited. This report presents the long-term results of our prospective study on the toxicities, health-related quality of life, and efficacy of whole-gland HDR prostate brachytherapy. Methods and Materials: Patients with biopsy-confirmed, magnetic resonance (MR)-visible local recurrent prostate cancer after previous external beam radiation therapy (EBRT) were eligible. Patients underwent MR-assisted, ultrasound-based whole-gland HDR prostate brachytherapy with a prescription dose of 21 Gy to the entire prostate and 27 Gy to the MR-defined intraprostatic target volume (TV) divided over 2 implants separated by 1 to 2 weeks. Adjuvant androgen deprivation therapy was not used. Results: Thirty patients were enrolled in the study. Median follow-up from salvage HDR was 72.0 months (10.7-121.5 months). Most patients (93%) had initial EBRT doses at conventional fractionation. The pre-HDR median prostate-specific antigen was 3.67 ng/mL (0.56-11.01 ng/mL). Seven (23.3%) were staged with prostate-specific membrane antigen positron emission tomography. Four (13%) required temporary urinary catheterization. There was only 1 (3.3%) grade 3 to 5 toxicity—a late grade 3 genitourinary toxicity. The prostate-specific antigen progression-free survival and freedom from androgen deprivation therapy rates were 73.0% and 93.0% at 3 years, and 24.8% and 69.6% at 5 years, respectively. Of the 26 patients who had a post-HDR MR imaging (median, 415 days), 9 (35%) had persistent disease. Of the 23 (77%) patients who had prostate-specific antigen relapse, 18 (78%) patients had disease at the TV confirmed by MR imaging, prostate-specific membrane antigen positron emission tomography, or targeted biopsy. Conclusions: Whole-gland salvage HDR brachytherapy with intraprostatic boost is well tolerated. Progression after salvage treatment was associated with local failure.
SN - 2452-1094
ER -