We welcome the two Editorial Comments discussing our recent meta-analysis evaluating the importance of local failure following definitive radiotherapy for high Gleason grade prostate cancer (1-3). We would first like to address the Editorial Comment from Mula-Hussain and colleagues, who discuss limitations of our study (2). Many of these limitations were reported as such in our original manuscript. We do of course acknowledge that our metaanalysis included trials that enrolled men many years

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... , which is an important limitation to consider. However, that fact has never prevented the conclusions from these trials influencing current care standards. Specifically, the results of the RTOG 9202 and EORTC 22961 trials defined the standard of hormone therapy in high-risk prostate cancer for decades following their publication (including to the present day) (4). All but the most recent trials of hormone therapy duration, in fact, utilized doses of radiation on the order of 70 Gy. For example, 70 Gy was the radiation dose used in the recently published PCSIV trial, which ultimately led to numerous professional societies allowing for 18 months of hormonal therapy as a minimal duration for high risk disease (5). Similarly, more than 50% of the patients enrolled on the recently published TROG 03.04 trial were treated to 66-70 Gy (6). A quarter of the patients on the EORTC 22991 trial, which was included in this meta-analysis, received 70 Gy (7). The large randomized RTOG 0126 trial, which had a standard-of-care arm dose of 70.2 Gy, was finally published in 2018 and failed to show an improvement in prostate cancer-specific mortality or overall survival (8). So long as the conclusions from these trials are still considered relevant, the use of lower dose of radiation in the studies including in our meta-analysis should not be used to inherently diminish the credibility of its conclusions. With regards to other technological advancements that were mentioned, such as MRI-guided treatment planning and use of hydrogel spacers, we agree that these may improve the risk benefit ratio of dose-escalation. However, none of these advancements were in place for essentially any of the large, published trials in prostate cancer radiotherapy. As with dose considerations, these technological advancements do not inherently detract from our meta-analysis. Other important limitations the authors mention are (I) the heterogeneity of the local failure definition and (II) the inability to account for the impact of the primary Gleason grade and secondary Gleason grade. The latter point in particular is important, and imbalances in bulk or grade of disease between those experiencing local failure and those who did not could have confounded the analysis. As a recurring theme, however, none of the prospective randomized trials in prostate cancer radiotherapy have thus far accounted for this difference, either. The limitations notwithstanding, we posit that there are two major conclusions from our meta-analysis, just as Levitin and Hamstra indicate in their Editorial Comment The first is that local failure is a poor prognostic factor even in high grade prostate cancer, despite the competing risk of distant failure. The second is that some patients experience a clinical local failure prior to experiencing a distant metastasis. One mechanistic explanation for this would be the so-called second wave theory, wherein a local failure seeds a distant metastasis. This would be supported by the results of the aforementioned RTOG 0126 trial, which