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User
Posted 21 Jan 2026 at 15:35

Hi everyone 

Just looking for some input ahead of an oncology appointment on Friday. Husband had RARP in Oct 23 in April last year his PSA rose to 0.32 but in July it went down to 0.28 and November down again to 0.24.

We are anticipating a  recommendation to start salvage RT... But has anyone ever waited.? His PSMA pet scan was clear. 

Any input would be greatly appreciated.

Thanks 

User
Posted 22 Jan 2026 at 11:21

Thanks all for your input. I have updated my profile with (hopefully) all the pertinent data. As you can see his PSA has jumped around quite a bit. Will update tomorrow after oncology appointment.

Thanks again

User
Posted 21 Jan 2026 at 16:03

Hi, Amelie.

As you aware  biochemical recurrence after surgery is PSA >0.2, and usually salvage treatment is considered. However, your husband's PSA has remained at low levels for 10 months and if anything is reducing.

I'm not medically trained but according to the eminent Dr Scholz,  your husband should be fine and not need further treatment.

https://youtu.be/JXRhzi0Z6qQ?si=SpZ03jiZ37nObKc1

Good luck? πŸ‘

User
Posted 22 Jan 2026 at 11:09
Recurrent PSA after an initial < 0.1 is usually missed cancer cells that replicate sufficiently to become detectable.

Sometimes "left behind" healthy prostate cells recover from the trauma of RP and start producing a small detectable amount of PSA a few months after surgery (this is what I was initially told I had). These should not keep increasing over time and certainly should not be exponentially doubling.

Persistent PSA post RP ie never going to <0.1 can be left behind healthy, cancerous or metastatic cells. BUT left behind cells producing a lot of PSA is most unlikely unless the surgeon completely botched the op.

So >0.2 post RP is most likely bad news and will need further treatment at some point.

User
Posted 23 Jan 2026 at 18:27
With regards to RT & diet - I had 32 sessions of RT to prostate and pelvic area. As with a number of things different hospitals have different ways of doing things. I was advised not to change diet, my diet was generally good and I didnt drink anyway, as they said its generally the change of diet that can mess things up, they want things to remain same as pkssible from planning stage onwards. They did suggest avoid wind producing veg though.

I did have bowel/bladder issues towards end of treatment and after. Had handful of 'accidents' whilst out despite emptying bowel etc beforehand. It did all clear up though. If I was to be out all day I'd have Immodium and that worked well.

As others may agree, different hospitals/onco!ogists advise differently go by what yours say is best.

Peter

User
Posted 23 Jan 2026 at 23:33
To answer your questions Amelie yes I think it is the correct response, I would also ask if pelvic lymph nodes are being included and the logic behind inclusion or not. I have personally had both approaches recommended to me by different oncologists, fortunately to date I have avoided either.

Regarding diet it sounds like they are recommending a low FODMAP style diet to minimise gas which can cause issues with alignment and also to minimise possible irritants. Personally I try and follow a ketogenic diet which is naturally low FODMAP to improve my metabolism, reduce insulin resistance and hopefully limit a primary food for cancer (Glucose).

Adrian, I took the win, no need to edit, keep up the good work and try harder next time πŸ˜‚πŸ˜‚.

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User
Posted 21 Jan 2026 at 16:03

Hi, Amelie.

As you aware  biochemical recurrence after surgery is PSA >0.2, and usually salvage treatment is considered. However, your husband's PSA has remained at low levels for 10 months and if anything is reducing.

I'm not medically trained but according to the eminent Dr Scholz,  your husband should be fine and not need further treatment.

https://youtu.be/JXRhzi0Z6qQ?si=SpZ03jiZ37nObKc1

Good luck? πŸ‘

User
Posted 21 Jan 2026 at 17:03
Think you must be drinking again Adrian! A PSA of 0.24 after surgery is not "low".

Amelie, the clear PET scan is good news as is a reducing PSA but those figures are much higher than they should be. The oncology appointment is important at this stage and I would want to know why the PSA is going down and what impact this will have on the likely SRT recommendation.

User
Posted 21 Jan 2026 at 17:20

Amelie, what was his post op PSA and what was his histology like, margins etc. It might be useful to list his PSA readings and dates in your profile. His pre op PSA was quite high,  I was frequently told a PSA of 20 is when you might get some spread. We don't very often see a PSA pattern like yours. I don't know if it is possible for the cancer to multiply then die. We have seen were the oncologist will let the PSA reach 0.5 before doing a PSMA scan. 

I had SRT without a scan ,there was something in the bed but we subsequently found there was cancer outside the bed in a pelvic lymph node. 

I said in my reply to you a couple of years ago, it might be worth a call to the nurses on this site, I think that advice definitely applies to your situation again. Hopefully your oncologist will have some answers when you see him.

Thanks Chris 

 

 

User
Posted 21 Jan 2026 at 17:27

Originally Posted by: Online Community Member
Think you must be drinking again Adrian! A PSA of 0.24 after surgery is not "low".

No mate, sober as a judge. πŸ˜‡

View Dr Scholz's video.

https://youtu.be/JXRhzi0Z6qQ?si=SpZ03jiZ37nObKc1

Right at the beginning of the video, he deals with, in his words, not mine 'low' post-op PSA  levels. Which he clearly describes as 0.1 and 0.2 levels, that remain stable. He, like we all, knows that ideally PSA level should be undetectable or at least below 0.1 after surgery, but adds an exception, to those with 'low' stable levels.

Amelie's husband has had similar 'low levels' that are actually getting lower over the past few months from 0.32 to 0.28 to 0.24. If patients continue at these levels, Dr Scholz clearly states they can still be deemed 'cured'. Again his word not mine.

Knowing that your levels have been hovering around 0.1 levels, and the understandable worry it's caused you, I was going to pass the video link to you by pm, to put your mind at rest.

Edited by member 21 Jan 2026 at 19:10  | Reason: Typo

User
Posted 21 Jan 2026 at 17:51
I really appreciate how much everyone cares and how supportive this community is. However, I can see how people’s responses are influenced by their own experiences. As someone whose husband was initially diagnosed after quite extensive spread, I can only suggest that, when considering what to do, you might want to ask: what if there is still cancer lurking in the pelvic region and we don’t do the RT β€” would we regret this later? Something to consider as you make decisions like this.
User
Posted 21 Jan 2026 at 18:38

Originally Posted by: Online Community Member
I really appreciate how much everyone cares and how supportive this community is. However, I can see how people’s responses are influenced by their own experiences.

Hi, Wife-of YM

On this particular conversation, my responses aren't based on experiences. Fortunately, I have not yet, had to deal with BCR. However, even after three years of being 'cancer free", it's something I'm still mindful of, and research.

It is, as you suggested, possible that Amelie's husband scan didn't pick up any mets, but it is also possible and probably more likely, as Dr Scholz has clearly explained, that some prostate tissue which was not cancerous, had been left behind, causing these 'low' and stable PSA levels.

If I were in Amelie's husband's shoes, I'd be asking, is salvage treatment necessary when my 'low' PSA levels are gradually getting lower, and my scan is clear. Is it possible that these levels are caused by prostate tissue that was left behind and non cancerous?

The only thing I'd like clarifying in Dr Scholz's video is, if a patient goes from undetectable PSA levels to 0.1 and 0.2 levels, are they viewed differently to patients who've always been at those 'low' levels after surgery?

Edited by member 21 Jan 2026 at 19:32  | Reason: Typo

User
Posted 21 Jan 2026 at 20:29
Hi Adrian,

I think you are amazing and incredibly helpful to everyone on here. I also totally understand this logic. And I do think it is very logical! Thanks to you I watch Dr. Scholz's videos myself and try to prepare based on those and I also calculate how long will this work, how long will that work... So I apologize if my comments seemed in any way disrespectful to you or to Dr. Scholz. Not intended. I am extremely grateful for your postings on here, and also for Dr. Scholz. There are many days that you both keep me going.

It was my own perspective I should have emphasized I was offering. Because in my household we live with a lot of wishing we had acted sooner, not missed signs that were there in retrospect...so I thought I should point that out that possibility, seemingly unlikely as it may be.

Hopefully on Friday Amelie's husband's oncologist will also help weigh the pros and cons of waiting. And the advice may well be to wait-and-see.

There are also others on this forum where waiting as long as possible has not only given them the best QOL, but probably also the longest.

User
Posted 21 Jan 2026 at 22:47

Originally Posted by: Online Community Member

So I apologize if my comments seemed in any way disrespectful to you or to Dr. Scholz.

Hi again.

Thank you for your very kind comments. I'm sorry if my reply gave the impression that I was somehow offended by something you'd said. That was not the case. Often comments on here can be 'lost in translation.' πŸ™‚

In Amelie's husband's case, I'd never heard of repeated post op PSA levels as high as his, which had not ben acted upon. I had always thought any three consectutive rises of PSA after surgery or a PSA level equal or greater than 0.2 was deemed BCR, and would normally trigger further investigation or salvage radiation and HT.

Before I posted my understanding of the situation, I thought I'd double check, and that's when I found Dr Scholz's video. It was the first time since I've been on the forum, that I'd heard anyone say that sustained and stable PSA levels of 0.1 and 0.2 levels may not be a concern and may remain at these levels for an indeterminate time.

Of course, on the other hand, such levels can often progress.

I'm not sure what the lady's husband's first post op PSA was, but she states about 5 months later, it had risen to 0.32.  However, over the last few months it has fallen to 0.24. His PSMA scan was clear.

I'm not medically trained, but I'd have thought, as his PSA is falling, and his scan is negative, and as Dr Scholz states that these low PSA levels can be harmless, salvage treatment might not be necessary?

It seems illogical that they'd start salvage treatment at 0.24 with a clear scan, when they held back at 0.32 and 0.28 levels when they were unsure of his scan results?

Unless there are other factors unbeknown to us, I'd be asking if my PSA could be further monitored, before having further treatment.

 

Edited by member 21 Jan 2026 at 23:18  | Reason: Typo

User
Posted 22 Jan 2026 at 08:09
Your logic is correct Adrian and yes stable PSA can be left untreated in the absence of any other symptoms / findings.

BUT it's very unusual and must be interpreted in association with the surgery pathology and full history which hadn't been posted here.

User
Posted 22 Jan 2026 at 10:21

Originally Posted by: Online Community Member

BUT it's very unusual and must be interpreted in association with the surgery pathology and full history which hadn't been posted here.

Hello again, mate.

I haven't a clue how unusual it is. Dr Scholz doesn't mention how common it is. He just classed non cancerous pre op PSA levels of 0.1 and 0.2 as exceptions to general cancerous causes of BCR.

As I mentioned in my early posts, we have limited information on Amelie's husband's post op histology and initial PSA results. As his medical team have been happy to monitor his situation for the past 10 months,  I'd have thought that his post op histology was favourable.  During that time, the steady decline in his 'low' level PSA and a clear PMAS scan, seem to justify their decision to hold back from any further treatment.

As I said, although my PSA has been 'undetectable' since my surgery three years ago. My post op histology wasn't good. Gleason 9 (4+5), cancer staging T3a (capsular breach and EPE) both factors which significantly increase the risk of BCR. On the plus side, I did have negative margins.

According to nonograms, despite being 'cancer free' for a long time, I'm still at quite a high risk of having to deal with BCR. That's why I'm particularly interested in folk on here who are in a similar position to me, and why I research the treatment options of those with BCR.

I've noticed recently, that unfortunately three posters, who had been 'cancer free' for the same time scale as me, have just been diagnosed with BCR. Which goes to show you can never declare, "I'm cured!"

I have followed your story closely, it is similar to a couple of others on here, who have have developed 'low' level PSA results, years after surgery and have been left with dilemma of whether they need salvage treatment or not.

I'm very pleased that your PSA seems to have stablised at these 'low' levels. I hope they continue to do so, mate, and that you never require salvage treatment.πŸ‘

 For those who have been 'undetectable' for years, then suddenly face possible BCR, I've never been able to establish, exactly where does the PSA rise comes from. Is it dormant mets that have suddenly sprung back to life, or are there other 'harmless' reasons that could cause these miniscule rises. Has anyone been able to identify exactly what caused yours?

I found Dr Scholz's video enlightening. Until viewing it, I didn't know there are post op men that can have stable 'low' level PSA that never causes any problems.  I would, however, like clarification on whether this group always had these  post op levels or does it include men, who like you and me, who were initially undetectable?

 Logically, I'd have thought, post op men who had stable 'low' level PSA, caused by harmless prostate tissue left behind, would have always shown 'low' level PSA and never developed it years later?

Anyway, back to Amelie's husband. I hope that he is in the unquantified group of men, whose 'low" level post op PSA, is caused by harmless prostate tissue left behind, and nothing more sinster. 🀞

Good luck.πŸ‘

Edited by member 22 Jan 2026 at 10:46  | Reason: Additional text

User
Posted 22 Jan 2026 at 11:09
Recurrent PSA after an initial < 0.1 is usually missed cancer cells that replicate sufficiently to become detectable.

Sometimes "left behind" healthy prostate cells recover from the trauma of RP and start producing a small detectable amount of PSA a few months after surgery (this is what I was initially told I had). These should not keep increasing over time and certainly should not be exponentially doubling.

Persistent PSA post RP ie never going to <0.1 can be left behind healthy, cancerous or metastatic cells. BUT left behind cells producing a lot of PSA is most unlikely unless the surgeon completely botched the op.

So >0.2 post RP is most likely bad news and will need further treatment at some point.

User
Posted 22 Jan 2026 at 11:21

Thanks all for your input. I have updated my profile with (hopefully) all the pertinent data. As you can see his PSA has jumped around quite a bit. Will update tomorrow after oncology appointment.

Thanks again

User
Posted 22 Jan 2026 at 13:15

Originally Posted by: Online Community Member
I have updated my profile with (hopefully) all the pertinent data.

Thanks for the additional information, Amelie.

It's interesting to see that your husband PSA levels were never deemed undetectable and that his PSA is fluctuating. Over the past two years, it does show a gradually rise but recent results show it falling.

Obviously his 'no clear margins' indicates some PSA producing cells were left behind. Unfortunately, positive margins are another factor that can increase the risk of BCR. 

I'm very interested in what decision your medical team decide to take. I've got a hunch they may decide to continue monitoring the situation, but I'm no expert.

I hope, whatever treatment plan is put in place, that there is no disease progression.

Best of luck for tomorrow. 🀞

User
Posted 22 Jan 2026 at 13:24

Thanks... It's certainly been a rollercoaster ride (and I'm not a fan!!!). 

Will update you tomorrow

Thanks again for the support and the video of Dr Scholz! 

User
Posted 22 Jan 2026 at 14:14

I think the P2+ no clear margins is actually P2+ N0 clear margins? There is a big difference in terms of interpreting the current situation but I will be very surprised if he doesn't get a recommendation for SRT either way.

 

User
Posted 22 Jan 2026 at 14:19

Francij, I thought the "no clear margins" was a  strange expression and wondered if the "no" could refer to something else. 

Thanks Chris 

User
Posted 22 Jan 2026 at 17:47

Hi Chris and francij.

Like you, I was also a little confused by the term 'no clear margins'. As far as I'm aware there are only negative or positive margins. I assumed, and AI agrees with my assumption, that 'no clear margins means' positive margins?

User
Posted 22 Jan 2026 at 17:54

Sorry... My bad interpretation! The margins were not clear... Hope that clarifies..?? There is so much medical jargon on all the reports!

User
Posted 23 Jan 2026 at 08:24
Good luck with your consultation today.

Confirmation the surgeon left something behind combined with a 0.2+ PSA guarantees the recommendation for salvage RT IMHO.

PSMA PET scans are not so good at spotting cancer next to the bladder because noise from the tracer results in a large "hotspot" in the bladder as the tracer is excreted. That may explain the negative scan. PS I was told this by my Oncologist after my scan so its not Google bollox.

User
Posted 23 Jan 2026 at 12:23

agree with frankij1 on this one...especially because you do not want to regret not having done that...

User
Posted 23 Jan 2026 at 17:02

UPDATE:-

The oncologist appointment was interesting. She has recommended 20-25 sessions of SRT. We asked about waiting as the PSA had actually gone down but her opinion was that treating it now was the best chance to get rid of it permanently... Is that accurate?? 

So my next question to anyone who has been through this, is about diet... Any tips,advice.. it's a complete shift to what we normally eat, wholemeal everything, spices, green veg etc... I don't think I own a recipe that doesn't have onions in it.... She has advised starting on the diet straight away to get the bowel ready for the changes... No alcohol too... 

Thanks everyone for your support and input, it is most appreciated.

User
Posted 23 Jan 2026 at 17:33

Originally Posted by: Online Community Member
Good luck with your consultation today.
Confirmation the surgeon left something behind combined with a 0.2+ PSA guarantees the recommendation for salvage RT IMHO.

Francij1 and Wife-of-YM. Congratulations, you got it right.βœ…οΈ

Amelie. I wish your husband the best of luck with his further treatment and hope that he makes a speedy and complete recovery. πŸ‘

As the PMAS scan didn't locate the 'rogue cells' did the consultant say where they were going to direct the radiotherapy? I believe, in cases like this, it's usual to target the prostate bed? 

Edited by member 23 Jan 2026 at 17:53  | Reason: Additional text

User
Posted 23 Jan 2026 at 17:57
Hi Amelie,

I'm sorry you and your husband are having to go through this, but my feeling is if one has the chance to kill off the cancer, one should take it. Especially because if you don't and it comes back, you might have major regrets and sadness about that...

My husband's doctors did not mention a thing about diet. My OH does not eat much in the way of processed foods, but he ate normally, and we went out for dinners with friends throughout a few week longer period of RT to the full pelvic region. He also probably had about a drink a day. Some days more than one, some days less (beer and wine, occasional whisky). BUT he did have severe bowel problems the last couple weeks. He still walked 5-10 miles/day and managed to time that with no accidents. The bowel problems were mainly in the afternoon and night. Maybe the dietary changes would help with that. But maybe not. It would be good to hear what others suggest about the diet during RT.

Good luck to you both. Especially hoping that in a couple months this puts an end to things and you can resume enjoying onions and feel more relaxed too.

And...this was not something I wanted to "win". Just want to see Amelie's husband rid of PC if possible.

User
Posted 23 Jan 2026 at 18:27
With regards to RT & diet - I had 32 sessions of RT to prostate and pelvic area. As with a number of things different hospitals have different ways of doing things. I was advised not to change diet, my diet was generally good and I didnt drink anyway, as they said its generally the change of diet that can mess things up, they want things to remain same as pkssible from planning stage onwards. They did suggest avoid wind producing veg though.

I did have bowel/bladder issues towards end of treatment and after. Had handful of 'accidents' whilst out despite emptying bowel etc beforehand. It did all clear up though. If I was to be out all day I'd have Immodium and that worked well.

As others may agree, different hospitals/onco!ogists advise differently go by what yours say is best.

Peter

User
Posted 23 Jan 2026 at 19:06

Originally Posted by: Online Community Member

And...this was not something I wanted to "win". Just want to see Amelie's husband rid of PC if possible.

Hi again Wife-of-YM.

This is our second 'misunderstanding' on this conversation. I misunderstood something you said earlier  and now you seem to have misunderstood me. We're having more misunderstandings than an old married couple. 😁

I'm just posting this to explain to others following this thread, who won't understand your comment on my use of "win"

When I first posted my last post, which was in response to Amelie's husband's consultant's decision to start him on salvage treatment. I wrote "Francij1 and Wife-of-YM You win. Well done! πŸ‘"  When I reread it, I realised that it could be taken as a churlish  comment, which it wasn't, so I changed it.

All I wanted to do was simply acknowledge that you and francij1 were right, and that your assessment of the situation was the one that the consultant took. I thought it would have been rude not to.

That's why I reworded that acknowledgement to "Francij1 and Wife-of-YM. Congratulations. You got it right βœ…οΈ " I actually edited my post before you posted your response to it.

Sorry, for any misunderstanding. πŸ™‚

Edited by member 23 Jan 2026 at 22:03  | Reason: More rewording. πŸ™‚

User
Posted 23 Jan 2026 at 22:00
Dear Adrian, This is a great forum, and we are all on Amelie and her husband’s side. I think that is clear. Everyone here knows that there are a gazillion options, and it’s bewildering and you feel alone and it's impossible to know which is the right one and which is the wrong one. We’ll never know. Personally, I think it's very helpful and positive that people like yourself, Francij1, and others can have different opinions on the right course of action because that is the reality we are all facing. Sometimes, we may have different ideas, but you are so thoughtful at researching each and every person's situation. Others dealing with advanced situations have different experiences. To me, even when people are offering differing advice it's clear you all have big hearts and are genuine and generously trying your best to help in a difficult and uncertain situation.

Back to Amelie, one more thing I wanted to add is that the radiation (in our case) though rough maybe for a few weeks (it is difficult to recall exactly how long) didn't impede life for so long. Other than the couple of bad weeks where he had to be very careful and was getting up a lot in the night, it was possible to adapt and still have good times and get our heads out of the situation. Each day you know it's getting closer to ringing the bell at the end of the RT.

User
Posted 23 Jan 2026 at 23:33
To answer your questions Amelie yes I think it is the correct response, I would also ask if pelvic lymph nodes are being included and the logic behind inclusion or not. I have personally had both approaches recommended to me by different oncologists, fortunately to date I have avoided either.

Regarding diet it sounds like they are recommending a low FODMAP style diet to minimise gas which can cause issues with alignment and also to minimise possible irritants. Personally I try and follow a ketogenic diet which is naturally low FODMAP to improve my metabolism, reduce insulin resistance and hopefully limit a primary food for cancer (Glucose).

Adrian, I took the win, no need to edit, keep up the good work and try harder next time πŸ˜‚πŸ˜‚.

User
Posted 24 Jan 2026 at 00:13

Originally Posted by: Online Community Member
Personally, I think it's very helpful and positive that people like yourself, Francij1, and others can have different opinions on the right course of action because that is the reality we are all facing.

Thanks again for your kind remarks.

It's often very difficult to comment on treatment, when you are not really qualified to do so. I don't think, apart from a GP who retired years ago, there is anyone medically trained posting on the forum. We once had an oncologist  who posted for a couple of weeks. I think he probably left because he got so many personal messages asking for advice. 😁 He had prostate cancer. I hope he's okay now.

It seems to me, that there are no certainties with any treatment. 

I agree with everything francij1 has said. Me and him, despite us taking the 'urine' out of each other, have been forum mates for 3 years now. I value and respect his opinion (sometimes 😁) As he said, any post op PSA reading of over 0.2 is deemed BCR and would trigger further investigation and possible salvage treatment. It's usually a bad sign, of mets or mirco-mets or cancerous tissue left behind, but as Dr Scholz clearly mentions there are exceptions, where PSA can be caused by benign tissue.

I know Amelie's husband had his consultation today, but I think if I were him, I'd still want to ask his consultant these questions:

How sure can you be that the cause of my PSA is cancerous cells? Could it, because of its fluctuation and decline over the last year be caused by benign cells? It's now only 0.24 could it be less than 0.2 when next tested.  If it drops below 0.2, is it still deemed to be BCR?  It seems to have peaked and is now declining, is it normal for cancerous cells to do this? You say that now is the best time to try and eradicate it. Why didn't you start treatment when it was at its highest 0.32, and it was rising at its fastest from 0.07? Why now, when its declining, when it's dropped by 0.08 from its peak? Why when the PMAS scan is clear, are you considering radiation therapy when there's nothing to target? Why the sudden rush, when nothing suggests there's going to be a sudden progression. What is your reasoning to act now?

Francj1 has stated that the PSMA scan can miss hidden cells in the bladder region. I don't dispute this. But I suggest IF there are any cancerous cells, it's far more likely that there are so few, that they can't be detected.

Dr Scholz states that there is a corelation between the likely sucess of a PSMA scan and post op PSA. There is a 10% better chance of detection for every 0.1 rise. So 0.2 is 20% and 0.9 is a 90%. ( I did a conversation on this with links, but now we've got no search facility, I cant find it! ) Based on this I'd be asking can't we monitor the situation for a while?  Can't we wait and see if my PSA continues to fall, or is it just too risky to delay? Even if, months ahead my PSA rises again, say to 0.5. Could I have another PSMA scan? Which according to Dr Scholz, would give a 50% chance of detection. We might then know if there are any mets, where exactly they are, and could accurately target them with radiation?

It might be that the clinicians have other reasons to act now, but I'd be asking what are they?

All patients have a right to question their treatment plan. Clinicians have a duty of care and should address any concerns you have. If they don't or you're unhappy with their response you can always ask for a second opinion.

Edited by member 24 Jan 2026 at 09:32  | Reason: Typo

User
Posted 24 Jan 2026 at 08:59

I've found the link I started on when's it best to start salvage treatment on BCR.

https://community.prostatecanceruk.org/posts/t31858-When-to-start-salvage-treatment-after-BCR#post309873h

 

Edited by member 24 Jan 2026 at 10:12  | Reason: Add link

User
Posted 25 Jan 2026 at 18:50

Hi Amalie

as it’s been said previously, everyone is different and copes differently. My hubby had his surgery in March 2022 and his PSA started to rise in August last year. Referrals back to oncology where we are are when PSA is 0.1. Fast forward to PET scan which showed cells in prostate bed (no other spread). 0.5cm blob. He has just completed 20 sessions of rt. At  end of Feb he will have completed 4 months of ht too (zolodex). I am not naive and very realistic and I thought we would get 2 good weeks under our belt as it were and then it may hit him a bit. He’s a fit and active 71 year old. Anyhow after 3 sessions he started to flag so it’s been a tough ride. In fact the last 5 it was almost as if body got used to it a bit. He opted for full pelvic rt to try and blast it once and for all. Bladder full and bowel empty was a challenge some days. Two weeks in, they suggested he change his diet to “beige” to help reduce bowel irritation. Zero fibre and white/beige food. The rt has been a challenge for him. No issues with bladder though, just bowel. Urgency to rush to the loo, lots of gas etc. so this week we will start to re-introduce fibre slowly slowly and see how we go. On the positive side, his hot sweats are less ferocious so he’s getting more sleep. In fact over the last 2 weeks he has made great progress so we feel we are now back on the road to recovery. Next PSA is beginning of Feb which we hope and pray will be 0 as he will still be on the ht. not sure when next one will be - 6 weeks or 3 months??? That one does panic me as he won’t be on any active treatment. It’s little steps for us. Wishing you the best xx

 
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