Hello Everyone,
First post for me after already gleaning some useful information from this community - thanks already!
My dad was diagnosed with Prostate Cancer at 62 in the USA. He had IG IMRT and brachytherapy treatment at the Dattoli Centre in Florida and 10 years on now he's still in the clear :)
When he was diagnosed, he was told that if he had any sons, they should start to have PSA monitored from the age of 40 to establish an early baseline.
So as the only son and at 40, I did as I was told (much to the initial amusement of my GP) and booked a PSA test at the end of October. Unfortunately the amusement quickly passed :( My first reading came back at 4.1. I was given a urine analysis and put on antibiotics whilst waiting for the analysis. That came back all normal so PSA was retested a couple of weeks later. Second reading came back at 3.3
Now I'm at the point where I've been referred to a Consultant Urologist who I asked (after reading some info on here) to do an MRI prior to any biopsy. I got my MRI results earlier this week and have been told that my Prostate has multiple 'suspicious' areas of change all over with the biggest area of concern measuring in at approx 8mm.
The Urologist told me that it's now time for a TRUS biopsy given (a) family history, (b) PSA and (c) MRI. I can't fault that logic and I'm booked in for early Jan but I do have some concerns which perhaps someone here has some advice on!
The concerns really stem from the fact that the Urologist indicated that should the biopsy come back positive (which I think looks likely), that because of my 'tender years', a radical prostectomy, in his opinion would be the only way forward.
Gulp! I'll be honest, at 41 (my birthday's been and gone during this initial process!) and with a younger wife and a 4 year old son, that kind of scares the living bejeezers out of me!
Presuming for now that is how this will play out, I'm wondering whether I should do anything else pre biopsy to give my future, as yet undetermined surgeon, the best possible information about my condition?
I asked the consultant whether a more detailed MRI (parametric style on a 3T scanner) rather than the 'basic' MRI I've had so far on a 1.5T scanner would be worthwhile. He said, 'No'.
I asked whether having a PCA3 test would be worthwhile. He said, 'Pfff £350, waste of money.'
I asked whether given the family history and for the benefit of both my current diagnosis and perhaps my son in the future, whether there was worthwhile genetic testing that might help understand the nature of my condition. He said 'Biopsy first, then you can sign up for ongoing genetic studies if you want - it's only blood tests'
By this stage I was getting the impression he wanted me to have a biopsy....!! Nevertheless, I asked whether there was any other testing or whether given his description of the 'multiple areas of concern and 8mm mass(?)' there was any benefit in a targeted biopsy rather than TRUS. He said 'no'.
I also wished I'd asked whether he could tell from the MRI whether the areas of concern where limited only to the prostate gland or showed any signs of spreading but I don't know if that's possible to determine anyway at this point?
I'd be more than grateful to hear from anyone who's got an opinion on this. Am I making a mountain out of a molehill by being unable to shake the feeling that more can be done diagnostically/imaging wise prior to traumatising the gland through biopsy?
So far everything has been handled through the NHS and I appreciate it's resources may be limited but I also have a comprehensive private health policy through work which I believe would cover any further 'necessary' diagnostics.
Apologies for the length of my first post - I'm not usually so self absorbed!
Cheers
Paul ('Big_Stan' to my 4 year old!)