Brachytherapy (BT), in the form of low-dose-rate (LDR) or high-dose-rate (HDR) BT, in combination with external beam radiotherapy (EBRT) is an excellent treatment option for men with high-risk prostate cancer (PCa). Earlier randomized trials have shown better disease control outcomes with EBRT + BT compared with EBRT alone. The recent randomized ASCENDE-RT trial, which compared dose-escalation EBRT alone to a total dose of 78 Gy vs EBRT + BT in men with intermediate-to high-risk PCa, showed that those treated with EBRT + BT were half as likely to develop biochemical failure at a median follow-up of 6.5 years [1]. The significant difference in biochemical failure-free survival, we believe, may lead to improved metastatic-free survival and overall survival with longer follow-up.More recently, two non-randomized studies added further weight to the oncological benefits of EBRT + BT over ERBT alone. In a population-based retrospective study involving 42 576 men in the National Cancer Database, Ennis et al. [2] reported that there were no differences in overall survival between men with high-risk PCa treated with RP and those treated with EBRT + BT plus ADT, but men treated with EBRT plus ADT had significantly lower overall survival. In a separate retrospective study pooling 1 809 men with Gleason 9-10 PCa across 12 tertiary institutions in the USA and Norway, Kishan et al. [3] reported that men treated with EBRT + BT plus ADT had significantly lower PCa-specific mortality and longer time to distant metastasis than men treated with EBRT plus ADT. EBRT + BT plus ADT was still associated with lower risk of distant metastases when compared with subset of men treated with dose-escalated EBRT to a total dose of ≥78 Gy plus ADT [3].This new evidence has the weaknesses typical of retrospective studies. Case ascertainment may be biased, or not representative of the population of men actively treated for PCa. There are many unknown confounding or biasing factors that could affect the observed results. Men treated with EBRT + BT, for example, were probably fitter and more suitable for a (relatively minor) procedure, compared with men treated with EBRT alone. Nonetheless, there are laudable aspects of these two studies: they are large population-based or multiinstitution, rather than single-institution studies, and they add weight to not just the ASCENDE-RT trial, but earlier randomized studies which showed the oncological benefits of EBRT + BT over EBRT alone. It would seem that, for men with high-risk PCa who opted for radiotherapy (RT), EBRT + BT is at least comparable, if not a better option than EBRT alone.Notwithstanding the level 1 evidence supporting improved oncological outcomes for EBRT + BT, this treatment seems to be increasingly less frequently used in practice. For example, the publicly available Medicare Benefits Schedules data showed a significant decline in the use of BT over the last 10 years [4], and the population-based PCa registry data showed that only 8% of men with high-risk PCa treated with EBRT received ...