MRI-Guided Ultrafocal HDR Brachytherapy for Localized Prostate Cancer: Median 4-Year Results of a feasibility study

Publication date

2019-08-01

Authors

Peters, MaxISNI 0000000460018149
van Son, Marieke
Moerland, RienISNI 0000000388861405
Kerkmeijer, Linda G WISNI 0000000393809169
Eppinga, Wietse S.C.ISNI 0000000389239685
Meijer, Richard PORCID 0000-0003-2510-7982
Lagendijk, J J WISNI 0000000393637862
Shah, Taimur T.
Ahmed, Hashim U.
van der Voort van Zyp, Jochem R NISNI 0000000393775683

Editors

Advisors

Supervisors

Document Type

Article

Collections

Open Access logo

License

taverne

Abstract

Purpose: For the treatment of localized prostate cancer, focal therapy has the potential to cure with fewer side effects than traditional whole-gland treatments. We report an update on toxicity, quality of life (QoL), and tumor control in our magnetic resonance imaging (MRI)-guided ultrafocal high-dose-rate brachytherapy cohort. Methods and Materials: Disease status was evaluated by systematic biopsies and 3T multiparametric MRI. The brachytherapy implant procedure under fused transrectal ultrasound/MRI guidance was followed by a 1.5 T MRI for contour adjustments and catheter position verification. A single dose of 19 Gy was delivered to the tumor with a margin of 5 mm. Genitourinary (GU) toxicity, gastrointestinal (GI) toxicity, and erectile dysfunction (ED) were graded with the Common Terminology Criteria for Adverse Events version 4.0. QoL was measured with RAND-36, European Organisation for Research and Treatment of Cancer QLQ-C30 and PR25. International Prostate Symptom Scores and International Index of Erectile Function scores were obtained. Prostate-specific antigen level was monitored, with biochemical recurrence defined as nadir + 2 ng/mL (Phoenix). Results: Thirty patients with National Comprehensive Cancer Network low- (13%) to intermediate-risk (87%) prostate cancer were treated between May 2013 and April 2016. Median follow-up was 4 years. Median age was 71 years (interquartile range, 68-73) and median initial prostate-specific antigen level was 7.3 ng/mL (5.2-8.1). Maximum Gleason score was 4 + 3 = 7 (in 2 patients). All tumors were radiologic (MRI) stage T2. No grade >2 GU or >1 GI toxicity occurred. International Prostate Symptom Scores only deteriorated temporarily. Mild pretreatment ED deteriorated to moderate/severe ED in 50% of patients. Long-term clinically relevant QoL deterioration was seen in sexual activity and tiredness, whereas emotional and cognitive functioning improved. At 4 years, biochemical disease–free survival was 70% (95% confidence interval, 52%-93%), metastases-free survival was 93% (85%-100%), and overall survival was 100%. Of intraprostatic recurrences, 7 of 9 were out of field. Conclusions: Ultrafocal high-dose-rate brachytherapy conveys minimal GU or GI toxicity and has a marginal effect on QoL. An early decline in erectile function was seen. Tumor control outcomes are poor (biochemical disease–free survival of 70% [52%-93%] at 4 years), most likely as a result of poor patient selection.

Keywords

Aged, Brachytherapy/adverse effects, Disease-Free Survival, Feasibility Studies, Humans, Kallikreins/blood, Magnetic Resonance Imaging, Interventional/methods, Male, Prostate-Specific Antigen/blood, Prostatic Neoplasms/blood, Quality of Life, Radiotherapy Dosage, Radiotherapy, Image-Guided/adverse effects, Time Factors, Treatment Outcome, Taverne, Journal Article, Research Support, Non-U.S. Gov't

Citation

Peters, M, van Son, M J, Moerland, M A, Kerkmeijer, L G W, Eppinga, W S C, Meijer, R P, Lagendijk, J J W, Shah, T T, Ahmed, H U & van Zijp, J R N V D V 2019, 'MRI-Guided Ultrafocal HDR Brachytherapy for Localized Prostate Cancer: Median 4-Year Results of a feasibility study', International Journal of Radiation Oncology Biology Physics, vol. 104, no. 5, pp. 1045-1053. https://doi.org/10.1016/j.ijrobp.2019.03.032