There is a confusing array of definitions of biochemical recurrence (BCR) after salvage radiation (SRT). I'm not sure that we're ready for a standardized definition yet.
The definition of SECOND biochemical ... - Advanced Prostate...
The definition of SECOND biochemical recurrence (after prostatectomy AND salvage radiation)
Since commencing study of PCa nearly two years ago I have been surprised at the focus on absolute PSA levels in defining thresholds for entering new treatments etc. Absolute measurements of any natural observable are fraught with difficulty - and PSA is worse than most because there are a variety of tests of different accuracies available.
To my mind, there is insufficient focus on PSADT - by going for the time-derivative, a lot of the background noise is filtered out.
I read a great 2008 paper out of Dana Faber noting that short PSADT men gained more from SRT than those with PSADT greater than 1 year - and then around that time all this seemed to fall into a void and researchers hared off in different directions looking at variables that might predict SRT efficacy... it's good to see SPPORT is stratifying men by PSADT and SVI, I suspect this will be yield some very interesting results.
Anyway... I think tracking PSADT through various treatments may be a sound idea, to get some sort of handle on how aggression may be evolving, and how quickly action may be required.
Stuart
For FIRST BCR, PSADT is useless because it is not validated for PSAs below 0.1, and most top ROs agree that SRT works best if used before that. MSK requires 3 values to fit to their log model, so if the goal is to find a clinical recurrence as early as possible, that increases the time delay. Also, PSADT has a great deal of variance for many individuals.