Go along with Tony and John T and others explanations and adding these factors in the real world mix:
If PCa is more aggressive or weird variant type(s) (sometimes never categorized correctly by Joe pathologist), or as PCa can morph to more aggressive strains via DNA-ploidy (changes in DNA chain= 3 categories of DNA prognosis types), so some versions of PCa do not give off much PSA's to measure, but a wise onco-doc monitors many other blood and urine parameters and/or methods to determine what might be happening. (this is also more rare among the whole population of PCa patients, but is one of the major exceptions in just PSA analysis). This is all related to the exceptions in PCa. Now as others mentioned psa can be a good measurement of disease tumor burden and esculations happening and effect the odds for detectable 'seeable' mets via scans, however micro mets can go unfound for years and years and scans miss those and so the docs assessment can be a huge guess and with unknowns.
PCa is complicated and the rule book is still be detected, thus some say first rule in PCa: 'there are no rules', there are generalizations and averages like in Partin tables and nomograms. They are still practicing medicine in effect, we went from the stone age, dark ages and maybe now are in the enlightenment stage, still miles from the perfection age. Scans are imperfect and so is total definitiveness in many areas of pathology, scans, psa and other analysis's.
**just an average Joe in my opinion in this stuff, so far have not seen anything to change that thinking, of course I did stay at a Holiday Inn Express last night (lol).** Opinions are like toliet paper, you can use them, you can roll with it, you can hold it and you can wipe away some bad stuff or flush it down, butt it is useful stuff and replaced neandrathal leaves used by prior Romans and countrymen: friends-Romans-countrymen lend me your ears!!!
Post Edited (zufus) : 12/2/2012 5:01:35 AM (GMT-7)