I'm interested in conversations about and I want to talk about
Know exactly what you want?
Show search

Notification

Error

Rise in PSA 6 years after RT

User
Posted 26 Jan 2024 at 09:49

(posted as a new topic as replying to one of my much earlier posts didn't get any comments)

I have not posted recently as all seems to have been going well. But for the last couple of years my PSA has started to rise from the 0.48 or so after I finished RT in 2016. I had my last PSA this month and this week the follow up telephone appointment from the consultant - this time the head of the department rather than her minions who usually call. PSA was 2.3 last July, it has now risen to 3.0. She didn't seem too concerned, noting that it is the rate of change rather than the actually value, which was important, but a 40% or so rise in six months seems a lot to me. When it initially started to rise it was suggested that they would do more tests when it got to 2, and I did have scans 18 months ago which showed all was well. She is now saying they will not do anything more unless it rises to 5 and I will have another PSA in six months.

I have no symptoms, no aches or anything. Urine flow remains reasonable at 2 to 3 visits during the night - she said that might not be related to the cancer anyway, just an enlarged prostate (King Charles take a bow..). Generally still in good health and doing weekly long walks in London.

Should I be worried?

User
Posted 26 Jan 2024 at 09:49

(posted as a new topic as replying to one of my much earlier posts didn't get any comments)

I have not posted recently as all seems to have been going well. But for the last couple of years my PSA has started to rise from the 0.48 or so after I finished RT in 2016. I had my last PSA this month and this week the follow up telephone appointment from the consultant - this time the head of the department rather than her minions who usually call. PSA was 2.3 last July, it has now risen to 3.0. She didn't seem too concerned, noting that it is the rate of change rather than the actually value, which was important, but a 40% or so rise in six months seems a lot to me. When it initially started to rise it was suggested that they would do more tests when it got to 2, and I did have scans 18 months ago which showed all was well. She is now saying they will not do anything more unless it rises to 5 and I will have another PSA in six months.

I have no symptoms, no aches or anything. Urine flow remains reasonable at 2 to 3 visits during the night - she said that might not be related to the cancer anyway, just an enlarged prostate (King Charles take a bow..). Generally still in good health and doing weekly long walks in London.

Should I be worried?

User
Posted 27 Jan 2024 at 00:35
Hi,

Yes different range of figures apply for men having Prostate and RT because a radiated Prostate will still produce some PSA.

Based on what we are told, I would also advocate a second opinion and a PSMA scan. There was a time when after radiation nothing was considered until PSA reached around 10 but the PSMA scan has meant that it is sometimes possible to find cancer earlier and further afield. A high quality MRI scan often enables residual or growing cancer to be identified in the Prostate.

Do let us know what you decide and with what result.

Barry
User
Posted 27 Jan 2024 at 08:33

Thanks for the comments. Last year it was just a CT scan and a bone scan even though I was expecting an MRI. I will have a think what is best to do, and maybe insist on an in person appointment since all the ones after lockdown have been telephone only.

Show Most Thanked Posts
User
Posted 26 Jan 2024 at 23:43

Hi,

From what I've seen an increase of 2 above the nadir or 3 increases in psa should be investigated.  Did you have a psma scan or an mri last year.  A psma scan can see smaller lesions and that should be preferred.  Some places don't like spending the money as they haven't got a psma scanner.

I've no experience of RT but if it was me I'd be looking for another opinion. Perhaps a PCUK nurse by phone or ask to meet an Oncologist at the hospital. Perhaps a private second opinion.

I was told I could have a psma scan at 0.5 on the NHS if it reaches that, after surgery. Also I could pay for one earlier.

There are more treatments available,, such a focal,  and I wouldn't want to miss out because it got too high.  If it rose by a third in 6 months it could become 4 by July and 5,2 by next Jan although you can't forecast accurately.

I wouldn't normally reply to an RT type query but I noted you said no-one replied to your last post. I had my treatment, surgery, around the same time as you and have been on here 7yrs so picked up some stuff and perhaps someone else will answer. All the best Peter

User
Posted 27 Jan 2024 at 00:35
Hi,

Yes different range of figures apply for men having Prostate and RT because a radiated Prostate will still produce some PSA.

Based on what we are told, I would also advocate a second opinion and a PSMA scan. There was a time when after radiation nothing was considered until PSA reached around 10 but the PSMA scan has meant that it is sometimes possible to find cancer earlier and further afield. A high quality MRI scan often enables residual or growing cancer to be identified in the Prostate.

Do let us know what you decide and with what result.

Barry
User
Posted 27 Jan 2024 at 08:33

Thanks for the comments. Last year it was just a CT scan and a bone scan even though I was expecting an MRI. I will have a think what is best to do, and maybe insist on an in person appointment since all the ones after lockdown have been telephone only.

User
Posted 27 Jan 2024 at 09:02

Hi Dave,

This is what I worry about in the future…that following RT my PSA will at some point rise and I may be on ADT for life. Do you mind me asking how long you were on ADT? I’m on it for 3 years, 9 months before RT and the rest after it, and if you been following me joint ache is now really affecting my QOL.

I hope you can get a satisfactory outcome. Do you have a CNS you can speak to? Mine are execellent.

Derek

User
Posted 27 Jan 2024 at 09:46
I was on hormone therapy for just six months before RT, it was decided not to continue afterwards. I did have a CNS for a while and during RT but have not had since and have lost touch with them, the original was based at the urology hospital not the oncology where I had treatment.
User
Posted 27 Jan 2024 at 11:27

Reading these posts it shows the difference in oncologists, in June last year my PSA was 0.49, in December it was 2.12.  I didn’t think she would worry to much about that.  She arranged for me to have a CT scan and nuclear bone scan which I had last Tuesday.

Arthur

User
Posted 27 Jan 2024 at 16:28

DH had brachytherapy 9 years ago. PSA went down to 0.01 where it stayed for many years. About 4 years ago it started to increase. Slowly at first. Consultant said he would see dh when it got above 2.1 DH phoned through his result when it was at 2.0. He still said no but to test in 3 months. 3 months later it was 2.7 so he had an MRI nothing showed, consultant said no cancer in prostate, so brachy had worked, however psa was now 3.7 So suggested DH had a psma scan, plus another psa test that came back at 4.9 so it was increasing quickly. The psma scan showed cancer cells in the lymph nodes in his pelvis and chest. I’ve still no idea how it gets into the lymph nodes further away without being in the nodes near the prostate. Gleason was 3+3 which apparently doesn’t spread. So who knows? So I would insist on a psma scan if you can. Your psa isn’t increasing very fast though, so hopefully all is ok. 

 

User
Posted 10 Mar 2025 at 20:25
One year on since I posted this, PSA increased between July and January from 3 to 7. They arranged bone and CT scans which they say shows no sign of cancer in the prostate or lymph nodes. I had not re-read this thread beforehand so did not have chance to ask about psma scans, maybe what you are saying is right and only psma would see residual cells at this PSA level. I have another PSA test in July and follow up appointment so hopefully will remember to discuss psma then (or I could do it earlier as I now have a named nurse who was in the room with us today).

On another issue I have just had a colonograph as a result of a failed bowel cancer test kit, blood in poo. This showed no cancer in the bowel. I received the full radioologist's report and far more technical terms than I should really be seeing. I thought I was just having my bowels scanned! yet this tells me I have a cyst on my kidney and gallstones but most of my other organs are fine. My main issue there seems to be diverticulosis - isn't this a side effect of radiotherapy? I am sure if there was something obvious in the prostate he would have mentioned it as well.

User
Posted 12 Mar 2025 at 07:08
No replies?......

Thinking more about this, I am not convinced the rise in PSA is anything to do with prostate cancer. If despite the PSA having risen significantly if there are any cancer cells there they have not grown to visible size in the three years since the last scans and presumably are too small to cause issues and if they continue to grow that slowly not cause issues in the future. More likely there is no cancer in the first place and all we are doing is trying to reduce a PSA rise which may be from unrelated causes. Going onto hormone therapy for this reason seems a tad extreme.

Or am I being too simplistic?

User
Posted 12 Mar 2025 at 11:19

Davews, I think I am right in saying PSA can come from healthy PSA tissue, cancer cells and a tumor. A very small amount of something, that looks like PSA can come from other sources. Infection and other inflammatory issues of the prostate can also cause the PSA to rise. 

Why not give the nurses on this site a call, you sound like you are going to need a to and fro conversation. The number is at the top of the page.

Thanks Chris 

User
Posted 22 Mar 2025 at 14:30

Just flicking through this thread.  Yes the prostate  that is left after radiotherapy will produce psa, and presumably if the prostate is a bit large will produce more.  I think the thing is though, prostate cancer cells produce more psa than healthy cells, so you could have no re-occurence of the cancer, but still having a rising psa, and as I understand it, it is the rate of the rise, or the doubling time that raises red flags.

What I have become inclined to do these days is err on the side of caution, scans and biopsies are not pleasant, but I would much rather have several of them and everything is normal, than think oh well might as well leave it and something is wrong. If I had taken that view about my active surveillance scan, and pushing for it, I'd not have been in the fortunate postion of having radiotherapy that is designed to be curative. 

User
Posted 22 Mar 2025 at 14:56

For dh nothing showed up in the lymph nodes at original diagnosis, he had mri and ct scan. It must’ve been in the nodes somewhere. Then when his PSA raised all these years later, again nothing showed on MRI. Dh then had the psma pet scan, this showed where the PSA was coming from, Dh has never been offered a bone scan, I’m assuming psma is better though. 

User
Posted 22 Mar 2025 at 15:38

Similarly for me, nothing showed in lymph nodes or seminal vesicles.  Before putting me forward for radiotherapy though, I had a nuclear bone scan where they injected dye and I had to wait for several hours, then went into the scanner.  This would have showed any metastatic cancer, and didn't.  Therefore they went ahead with the radiotherapy plus hormone therapy ongoing for 9 more months.  After the radiotherapy ends next week, not sure what I will get after that. 

The problem with any cancer is that it can return, even though it was supposedly got rid of initially.  This is why they will never say you are cured, only in remission.  It may be that whatever is inside that particular body, which predisposed them to get the cancer in the first place, is still there because you are as you are.  Hence why it can return after many years.  

I know several people who have had breast cancer, not a genetic one, who had surgery, radiotherapy, hormone treatment for 10 years and were supposedly 'cured'.  But it came back.  I do think though, that anyone who is not happy, or concerned about the way they are being managed, should ask for a second opinion, it is something you are entitled to.  I am very much of the opinion, if something doesn't feel right, it's your body listen to it. 

User
Posted 22 Mar 2025 at 16:51

John1234 dh’s psma scan showed no cancer in his prostate or local nodes. Only nodes higher in abdomen and chest, so this means that the brachytherapy worked 9 years ago as there’s nothing in prostate, so the fact it’s in the nodes means it must’ve been there all along, even though his PSA was 0.01 for 5 years after. DH has been gene and has the brca2 gene. 

 
Forum Jump  
©2025 Prostate Cancer UK