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Active monitoring MRI results waiting time

User
Posted 13 Nov 2025 at 08:20

Anyone know how long the wait for MRI is these days? I know that's a bit like asking how long is a piece of string, but I've been waiting 9 weeks and wondering if I should say something. I am on active monitoring for gleason 3+3 Grade 1 at UHCW (Coventry). 

First diagnosed in 2021 but PSA in July this year was 9, which was twice the level in 2021 and prompted urologist to order a scan for possible growth/spread. I just turned 73.

My last MRI was in 2024 and the results letter said: "Your MRI was unremarkable. You do have some lower urinary tract symptoms but would not consider radical surgery in view of these."

I realise that, relatively speaking, I am in good shape, but speaking of relatives my younger brother has just started hormone therapy after a prostatectomy. So I am a little anxious. 

Stephen

User
Posted 13 Nov 2025 at 09:30
Well that was weird! An hour after I posted this I got the results. That was eight weeks to the day from the MRI.

"Thank you for attending for multi parametric surveillance MRI of your prostate. This shows changes, which suggest a more significant cancer than your known grade group 1 (Gleason 3+3) cancer. In light of this I recommend transperineal biopsy, which I have booked for you. [Next Monday]."

So, on we go.

User
Posted 13 Nov 2025 at 09:52

Hi,  Stephen.

I was just about to reply to your first post. 🙂

I'm sorry to hear that the MRI suggests some sort of disease progression, that's deemed worthy of further investigation. I've read your old posts and see that you had difficulties with your last biopsy. I hope things go more smoothly this time and that it reveals your cancer is still low grade.

As far as I'm aware, the MRI cannot detect a increase in cancer grade. Did it give the size of your prostate. As you are probably aware an enlarged prostate (BPH), prostatitis, or UTIs can cause elevated PSA levels.

At least, AS has given you four years of avoiding possible side effects of any radical treatment that you now may require.

Good luck and please keep us informed.

User
Posted 14 Nov 2025 at 08:29
Many thanks Adrian, that was all very helpful. I am about to engage with my urologist on this and explore my options.

I continue to be concerned about the fact that urologists and cardiolgists can't definitively agree on how to handle atrial fibrilation patients like me who are on Apixaban or other anticoagulants.

My first biopsy led to the worst medical trauma I have ever experienced. Who knew that not being able to pee because there were blood clots in your bladder could be so painful. My wife had to rush me to A&E and I spent four extremely distressing days lying in a pool of my own blood in a hospital bed sporting the thickest of catheters (a 'three-way' used for pumping out the bladder, which is as horrible as it sounds.

So I will ask "what's the alternative?" but also "could the biopsy lead to anything other than a decision to remove my prostate?" Frankly, I have lived with the possibility of a prostatectomy for more than four years (my brother had his five years ago). I'm now 73 and somewhat resigned to this anyway.

Thanks again for your help and encouragement.

Stephen

User
Posted 14 Nov 2025 at 09:56
I to have A-Fib and put on blood thinners a few years ago. Edoxaban I think.. I was told to stop the thinners 2 days before my transrectal B. I decided to stop 4 days before. I ask when to restart my med. and they suggested 3 days later. So Friday biopsy and I took a tablet on the Monday. Up until then I had no show of blood which was great. Anyhoo Tuesday morning first pee looked like Texas Chain Saw Massacre. Blood evident throughout the day but slowly turned to pink urine. I did NOT take a thinner the following day and all returned to normal.. I'm going to try again tommorow Saturday, or Sunday and see what happens.

Good Luck Dave

User
Posted 14 Nov 2025 at 10:34

Hi again, Stephen.

Like you, I've got a family history of prostate cancer. My dad, had it, and both me and my younger brother were diagnosed with the disease. My brother opted for radiotherapy and hormone treatment. Six years later he's fine, and has had no recurrence. 

I went on active surveillance. After a couple of years they discovered significant disease progression. I ended up having robotic surgery. Three years after the operation, I'm doing fine and have, touchwood, had no recurrence

If you read my profile and this link, you'll see my PCa history.

https://community.prostatecanceruk.org/posts/t30214-Almost-a-year-on-after-RARP

I must emphasis that I'm not medically trained, mate. The advice I give is purely based on my own experiences and what I've learned over the past few years, from reputable sources.

Your family history of the disease may increase your risk. In the grand scheme of things your PSA level is elevated, but not drastically so. For a man of your age, anything above about 6.5 is deemed abnormal. Elevated PSA can, and often is, due to other non-cancerous prostate conditions, like an enlarged prostate (BPH) prostatitis, and urinary infections.

Did your clinicians, rule out non-cancerous conditions for your PSA rise. If so, was that the reason they sent you for an MRI scan or was the scan a routine follow up as part of your active surveillance monitoring?

This MRI has shown ' more significant cancer than your Grade 1, Gleason 6 (3+3)'. This comment mystifies me. As far as I'm aware, an MRI scan can show apparent visible disease growth, but it can't show any difference to your the Grade or Gleason score. Only a biopsy can show histological changes. 

I'd have the biopsy, mate and wait for the results, before worrying about the need for any radical treatment.

The experience of your first biopsy is bound to make you anxious about another. If I were you, I'd ask to have one under general anaesthetic. It's how they did my second biopsy. I didn't feel a thing.

The biopsy will dictate whether you need further treatment, it may also conclude that you are safe to remain on active surveillance.

IF you need further treatment here is an excellent link to treatment options and possible side effects.

https://youtu.be/zYTU94-8pTc?si=1Z29_l8rbTwF6DHl

Good luck, mate, and please keep us updated. 👍

Edited by member 14 Nov 2025 at 11:25  | Reason: Add link

User
Posted 14 Nov 2025 at 12:03

Thanks for sharing Dave. Very interesting that the blood problem increased after you went back on the anticoagulant, because that is what happened with me. I have now asked my urologist to talk to my cardiologist.

 

Very interesting that the blood problem increased after you went back on the anticoagulant, because that is what happened with me. I have now asked my urologist to talk to my cardiologist.

Sidenote: the urologist that treated me when I was admitted with the “blood clots preventing peeing” problem, was quite disparaging about cardiologists because, in his opinion, they haven’t done the homework on how to handle patients who are on the newer anticoagulants. Basically, those anticoagulant are very helpful to cardiologists, but a minefield for any doctors that have to do surgery, from the dentist to the urologist.

good luck and take care

 
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