Latest PSA Test.

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Some good news today, which I thought I would share, as good news from any of the forum members gives me a lift, and I hope it does for other members, too.

My last blood test, on 24/09/2026 was again <0.01, or undetectable (you were right  ).

The full sequence of tests since I finished radiotherapy has been like this:

04/04/2025 = 0.05

04/09/2025 = <0.01

20/03/2026 = <0.01

24/09/2026 = <0.01

My treatment has been 6 months hormone therapy, 37 fractions of EBRT totalling 74Gy, to be followed by hormone therapy out to 3 years from diagnosis.

On 11/04/2024 the PSA level was 7.19. My grading at diagnosis was T3b N1 M0. The node concerned was directly adjacent to the prostate. 

I am being treated with "curative intent", and it looks to me that I am currently on the right pathway.

The hormone therapy has given me the usual side effects. We both find the magnifying glass my wife keeps at her bedside hilarious.

I'm an not going to complain though - mainly because no one listens.

It does seem to me that Zoladex (goserelin) is doing the job. Would I be wrong to think that different formulations hit different spots?

All in all I hope this encourages others the way it has encouraged me.

  • Great news, congratulations. Long may it continue.

    Made in 1956. Tested to destruction.

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  • Great news  - regarding the magnifying glass, are you taking Tadalafil daily tablets?  I’m surprised if this is the case.  Not sure if any other form of ADT would help in this area.  AW

  • Great news  . My onco described a PSA test of <0.025 as “excellent news”. I’m on Zoladex for 3 years too…and on a treatment pathway the same as yours. Fingers crossed the level stays steady and low for us both…!

  • Great news  I wish you many many more PSA tests with this result.

    Kind regards - Brian.

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  • Thank you for your encouragement.

    I am not taking any Tadalafil, or other medication which might help with erectile dysfunction.

    My better half has significant problems “down there”, resulting from a difficult child birth some years previously, so penetrative sex had been a thing of the past for some years. 

    We had found other ways to preserve intimacy and were purring along quietly when I was diagnosed with PC. 

    I already take multiple medications for hypertension and back problems and didn’t really want to add more.

    I was one of those whose libido went walk about completely so, in consultation with the oncologist I made a conscious decision not to care much.

    It is not something I discuss here because I am aware that many couples have real problems in this area, and it seems that my personal journey is different to many.

    Thank you again for your encouragement in all that you say, and the advice you offer.

    Although my separate back problems have caused me significant problems, your capacity to walk up mountains has been a real example.

    Following your experiences and setting my own rather less ambitious has brought me from almost bed bound 18 months ago to a reasonable steady 5k daily on the flat.

    Steve

    Changed, but not diminished.
  • Following your experiences and setting my own rather less ambitious has brought me from almost bed bound 18 months ago to a reasonable steady 5k daily on the flat.

    Wow  that is quite an achievement, don’t play it down in any way … well done you!  
    Thank you also for explaining about not using Tadalafil.  As you know, I’m an advocate for using it to stop atrophy, as well as helping the sexual side.  Mrs AW and I managed to preserve function for bedroom action during ADT (including much encouragement at times due to lack of libido on my part) but that put us in a great place once ADT stopped and libido returned.   AW

  • Hi mstev2,

    That's great news about your latest PSA reading - long may that continue.  I also loved your reasoning about not complaining because no one listens.  There's a lot of truth in that outside of this forum.

    Best Wishes

    Brian