Prostate
One descriptive high-risk benchmark and no randomised readout, so the 5-yr BCR-FS of 44% is a reference point for trial design, not a comparison.
PROTEUS
ForHigh-risk prostate cancer, perioperative setting
TL;DR5-yr BCR-FS 44%, MFS 71%, CSS 92% at 60-mo median f/u in a real-world high-risk prostate cancer benchmark cohort.
Also covered May 31
7 details 1 trial watching
Design not stated in source; described as a real-world benchmark. Median follow-up 60 mo.
Reported: 5-yr BCR-FS, 5-yr MFS, 5-yr CSS. No primary endpoint or effect size stated.
Framed as a reference point for perioperative treatment strategies in high-risk disease, not a test of one. Useful only once the cohort definition and treatments received are known, since those determine which trial populations it can benchmark.
| Endpoint | 5-yr estimate |
|---|---|
| BCR-FS | 44% |
| MFS | 71% |
| CSS | 92% |
Descriptive benchmark with no comparator, N, eligibility, or treatment details in source; cannot classify impact on any perioperative decision.
- Which perioperative strategies improve on this BCR-FS benchmark? active COACTION Trial - COmbination Androgen bloCkade in inTermediate to hIgh-risk prOstate caNcer Phase 4n=144 ยท primary completion 2026-03 ยท RCT neoadjuvant leuprorelin+darolutamide pre-RP, pCR EP
- Cohort high-risk definition and treatments received
๐ Sources ยท ๐ฆ 1 tweet
๐น Median follow-up: 60 mo
— Can Aydogdu (@CanDAydogdu) August 28, 2026
๐น 5-yr BCR-FS: 44%
๐น 5-yr MFS: 71%
๐น 5-yr CSS: 92%
Providing a real-world benchmark to contextualize perioperative treatment strategies in this high-risk population.
๐ https://t.co/NyszMg9uCA#ProstateCancer #PROTEUS #Urology