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Gleason 6, AS or immediate treatment?

User
Posted 21 May 2024 at 09:36

Hello friends i am 52 years now, I write my case here to receive some advice since
I have verified that many users here have a lot of knowledge...


Diagnosed with gleason 6 (3+3). MRI PiRads 4 (10x11 milimeters). PSA 5.33 ng/ml.
Systematic biopsy with total 14 cores and 5 cores targeted to the lesion (3 positives & 2 negatives). Core with the greatest impact is 60%.
35% tumor involvement of all the material sent. Rest of prostate without evidence of malignancy.
I'm really terrified not knowing what to do.


In psychological treatment since then, asking various specialists... private healthcare pushing towards surgery and national healthcare towards AS.


I feel that urinary incontinence and ED are going to take over me from a very young age and the logical fear of future metastases. I am terrified for te surgey, and I don't see RT as a good option for me.


Welcome your opinions ...


BR. 


quique.

User
Posted 22 Jun 2024 at 13:08
Just remember that the urologists almost always push for RP surgery and the oncologists almost always push for RT. It's the nature of the beast. The bottom line is that in most cases the results are the same - ie curative - but individual cases may respond better to one or the other treatments.
I found it hard to get a truly unbiased opinion as neither seem to communicate with each other and they each only fully understand their own speciality.
User
Posted 21 May 2024 at 15:05
Yes, friend.... this video https://www.youtube.com/watch?v=mnHGyEsxXO4 and this https://www.youtube.com/watch?v=aotF2SPzCmU They seem quite forceful and Dr. Scholz is a prestigious doctor
User
Posted 22 May 2024 at 11:22

Originally Posted by: Online Community Member
i looked at focal therapies extensively but wasn’t suitable as my disease was in all four quadrants of the prostate.


Hello again mate


If cancer was detected in all four quadrants of your prostate you were T2c. 


NICE used to class T2c disease, no matter what the grade or volume as high risk and not suitable for AS.


However CPG did away with T2 sub grades and put T2a, T2b and T2c,  all as T2. NICE when adopting CPG, then suddenly, overnight, changed  the old T2c to low risk, suitable for AS.


I found this totally mystifying, especially as research has indicated that T2c disease, being bilateral disease, is much less likely to be the predominant factor, more significant than PSA levels or Gleason score, in AS failure.


Here's a conversation on the subject, which contains links to the aforementioned statements.


https://community.prostatecanceruk.org/posts/t29997-T2c-disease-and-active-surveillance


 

Edited by member 22 May 2024 at 11:56  | Reason: Additional text

User
Posted 22 May 2024 at 14:29

@quique


Good to hear from you.


Indeed there are striking parallels. 


I think my prof mentioned in ~44%  cases the cancer type is usually upgrades. In my case he postulated this would be ~60%. Knowing this pushed me to surgery as I had a hunch time was of the essence.


Its a difficult journey to say the least. I hope all the information helps like it did me back in 2019 as this community is fantastic.


btw if you go down the surgical I'm more than happy to ask my prof if he knows surgeons in your locations that use retzius sparing and/or neuroSAFE as I beleive he does the surgical training/education circuit all across EU/US/Asia.


 


 

Edited by member 22 May 2024 at 14:39  | Reason: Not specified

User
Posted 22 May 2024 at 14:37

@Adrian56 Totally agree. Its what set off alarm bells....after London MDT review two options were recommended....AS or RARP. My ex is a researcher in this field so our pillow talk used to be cell pathology, angiogenesis and cribriform cell structures :D


Knowing my PCa was at least T2c I engaged for a second opinion with the Prof Whocannotbenamedonhere as thats seemed like the minimum due diligence. The prof mentioned there was a ~60% chance there would be cribriform gland cells (>=grade 4) on final histology and he was spot on. Acting fast was prudent it would seem as the Prof had to resect additional tissue around the bladder neck and the cancer was extremely close to breaking out of the prostatic capsule.


I count my lucky starts I didnt defer for a couple of months over the xmas period which would have taken me into the covid crisis.


Happy days thus far....


 

User
Posted 13 Jun 2024 at 10:20

Hi 


I have followed your thoughts about the the best choice to make and after affects.I was PSA 2.19 Gleason 3+4=7


at the age of 70 with 5 cores out of 20 positive and was offered Robotic surgery or Brachytherapy and took Brachytherapy as i felt that the side affects may be better.


I am 8 years on in September and think i have had a very good result with no real side affects.


There are no guarantees in any option but if you do go for AS please keep on top of it as a few on here left it to long before making a decision and regretted it.


If you click on my Avatar you can see my Journey and i am happy to answer any questions about it, but i am no professional so can only give my side.


Good luck. John.

Edited by member 13 Jun 2024 at 10:21  | Reason: Not specified

User
Posted 22 Jun 2024 at 11:50

I was diagnosed gleason 6 about 3 weeks ago. Prior to my diagnosis I had pretty much decided on AS, if I was Gleason 6. On a fact finding visit to the Radiotherapy Team this week I was told a mistake had been made and I was actually Gleason 7 (3+4), which was (another) shock. However, I was pleasantly surprised when the most likely side effects (for my personal situation) were properly explained. I have BPH (66cc) and psa 5.5, so 3 months hormone treatment followed by 4 weeks IMRT/IGRT, 2 more months hormone treatment has been suggested. I'm weighing things up, but this potential exit strategy from AS has made me more relaxed and less anxious. Based on my experience alone, I'd suggest a chat about RT with a professional. I also have a prearranged meeting with a surgeon next week to discuss removal and staying on AS. Trying to keep an open mind till then, but as I say I felt much better after talking to the Radiotherapy Team.

User
Posted 25 Jun 2024 at 10:14
A curious case just happened to me now...
In addition to the prostate I am on a follow-up program to monitor a pelvic cyst that requires annual pelvic MRIs.
In the MRI report from 2 weeks ago, the radiologist talks about the prostate as well and compares it with the results from 1 year ago.

Well, the surprise is that it says that I have triangular morphology lesions in both prostate lobes, compatible with prostatitis changes and that remain stable compared to the MRI from a year ago.

Between both pelvic MRIs, a multiparametric MRI in October 2023 was performed in another hospital due to a rise in PSA, which only saw a 10x11 millimeters (square) unique pseudonodular lesion in the left peripheral lobe.

Therefore... in different hospitals, with different radiologists, with different scanners, you see different things... and now what...?

This is crazy!!
User
Posted 30 Sep 2024 at 22:49

Such a rapid rise could be an infection especially with the semen symptoms. It is very rare for prostate cancer to change so rapidly.

Dave

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User
Posted 21 May 2024 at 10:17

Hello mate.


Welcome to the forum. I'm sorry that you've had to find us but glad you have.


We are not clinicians and views on suitability of AS vary a lot on here. I believe there is no doubt that the AS option is becoming and more frequently used.


https://www.cancer.gov/news-events/cancer-currents-blog/2022/prostate-cancer-active-surveillance-increasing 


The ProtecT Trial focused on a huge sample of men with low grade, low volume cancer and compared the outcomes of those electing surgery, RT/HT or Active Surveillance. After 10 years, it transpired that there was very little difference in the outcomes of the 3 treatments.


It appears that thousands of men are having radical treatment when it may never be required.


I was initially diagnosed with cancer that met the criteria for AS. I thought it was a no brainer to take that option. Unfortunately I was amongst the 30% who fail AS. My disease progressed and I ended up having surgery.


For those selecting AS my only strong advice would be make sure the surveillance is active and ensure that you are being monitored correctly, with follow up PSA checks MRIs etc.


You do need a certain mindset for AS. You've got to be able to live knowing that you have the disease, and knowing that it may progress. Personally I found the anxiety of AS a lot easier to deal with than the anxiety of recurrence after surgery.


Best of luck with whatever you decide.


 


 

Edited by member 21 May 2024 at 10:43  | Reason: Typo

User
Posted 21 May 2024 at 10:22

Hello mate, thank you very much for your response.
I had already read the article you sent... very interesting...
In my case, I can't tell if I have a high or low volume of Gleason 6 cancer. The lesion is 10x11 millimeters but of the 5 cylinders on it, 3 have tested positive and the largest with 60% involvement.

Therefore, not all of the lesion is cancerous in its entirety...

B.R.
User
Posted 21 May 2024 at 10:32

Originally Posted by: Online Community Member

In my case, I can't tell if I have a high or low volume of Gleason 6 cancer. The lesion is 10x11 millimeters but of the 5 cylinders on it, 3 have tested positive and the largest with 60% involvement.


As I said I'm not medically qualified. It would inappropriate for me to comment on the exact nature of your specific disease and the risks involved for you to opt for AS.


All I'm saying is, if my clinicians told me I was suitable for AS, it is the option I would take. The beauty of AS is you can always opt out and elect radical treatment if the need arises.

User
Posted 21 May 2024 at 12:01

Originally Posted by: Online Community Member


Hello friends i am 52 years now, I write my case here to receive some advice since
I have verified that many users here have a lot of knowledge...


Diagnosed with gleason 6 (3+3). MRI PiRads 4 (10x11 milimeters). PSA 5.33 ng/ml.
Systematic biopsy with total 14 cores and 5 cores targeted to the lesion (3 positives & 2 negatives). Core with the greatest impact is 60%.
35% tumor involvement of all the material sent. Rest of prostate without evidence of malignancy.
I'm really terrified not knowing what to do.


In psychological treatment since then, asking various specialists... private healthcare pushing towards surgery and national healthcare towards AS.


I feel that urinary incontinence and ED are going to take over me from a very young age and the logical fear of future metastases. I am terrified for te surgey, and I don't see RT as a good option for me.


Welcome your opinions ...


BR. 


quique.



I am 54 and Gleason 4+3. My advice would be, don't panic! Incontinence risk is very low, and even if there were any it would likely be very occasional and minor. Metastestes, can't say, but they should be doing scans to look into that, and with "only" 3+3 I'd say you're in a good position. I was lucky to get a PSMA PET scan which is 95% accurate and mine is deemed localised. If yours proves local, I'd say even Active Monitoring without radical intervention. Have they already recommended a treatment option?
Things that helped me:
* Speak to a Prostate Cancer UK nurse on the number at the top of this page
* You can get overwhelmed with all the info online, but personally I trust the info from the PCRI channel on YouTube (go to YouTube and search PCRI). They cover all the options in great detail

User
Posted 21 May 2024 at 12:18
Hello again.. thank u for fast answers...

As I said, some doctors push towards radical surgery treatment and others towards active monitoring... there is no consensus.

There are studies that support that the metastatic capacity of 3+3 is close to zero, but unfortunately we only know this when we remove the prostate with all that this implies.

It is then difficult to understand and suffer undesirable side effects derived from surgery due to a non-dangerous disease. What would be the main justification for treating it?
User
Posted 21 May 2024 at 12:34

Originally Posted by: Online Community Member
Hello again.. thank u for fast answers...

As I said, some doctors push towards radical surgery treatment and others towards active monitoring... there is no consensus.

There are studies that support that the metastatic capacity of 3+3 is close to zero, but unfortunately we only know this when we remove the prostate with all that this implies.

It is then difficult to understand and suffer undesirable side effects derived from surgery due to a non-dangerous disease. What would be the main justification for treating it?


The main justification for treating it would be if it's in danger of spreading and from my uneducated viewpoint, it doesn't sound like yours is. What scans have you had or are you getting? I would say you're in a good position mate, and don't feel rushed. Prostate cancer is very slow, it's normal to take a few months to explore the million options.. I have. Get your scan results, but don't feel pushed into surgery.

User
Posted 21 May 2024 at 12:37
Since I was diagnosed in December 2023, the recommendation is to do the first PSA now in May after the diagnosis and as of today nothing else has been done...
User
Posted 21 May 2024 at 14:16

Originally Posted by: Online Community Member
Since I was diagnosed in December 2023, the recommendation is to do the first PSA now in May after the diagnosis and as of today nothing else has been done...


Get onto it, don't make any decisions without more info. Thankfully they fast-tracked me and I had CT Scan, biopsy, and bone scan all within a month. PSMA PET scan as well since then. I would have thought the CT scan is the minimum they should have done for you. Or else they're already super confident that nothing has spread!?

User
Posted 21 May 2024 at 14:20
Hello friend MRI and biopsy says all is inside prostate... nothing spread!!
User
Posted 21 May 2024 at 14:32

Originally Posted by: Online Community Member
Hello friend MRI and biopsy says all is inside prostate... nothing spread!!


My feeling would be surveillance. Ask them if this is a reasonable option for you. Look at the YouTube channel I mentioned, or other online info.

User
Posted 21 May 2024 at 15:05
Yes, friend.... this video https://www.youtube.com/watch?v=mnHGyEsxXO4 and this https://www.youtube.com/watch?v=aotF2SPzCmU They seem quite forceful and Dr. Scholz is a prestigious doctor
User
Posted 21 May 2024 at 17:07

The doctors' main justification in my case for doing the surgery is that now it would be a simpler surgery and if we try later when the tumor is larger or more aggressive... the surgery will be more aggressive.


So the question is... is it worth taking the risk of possibly having more side effects in the future
to gain a time of maximum quality of life without side effects in the short term?

What is your opinion?


 


Originally Posted by: Online Community Member


Originally Posted by: Online Community Member
Hello again.. thank u for fast answers...

As I said, some doctors push towards radical surgery treatment and others towards active monitoring... there is no consensus.

There are studies that support that the metastatic capacity of 3+3 is close to zero, but unfortunately we only know this when we remove the prostate with all that this implies.

It is then difficult to understand and suffer undesirable side effects derived from surgery due to a non-dangerous disease. What would be the main justification for treating it?


The main justification for treating it would be if it's in danger of spreading and from my uneducated viewpoint, it doesn't sound like yours is. What scans have you had or are you getting? I would say you're in a good position mate, and don't feel rushed. Prostate cancer is very slow, it's normal to take a few months to explore the million options.. I have. Get your scan results, but don't feel pushed into surgery.


Edited by member 21 May 2024 at 17:09  | Reason: Not specified

User
Posted 22 May 2024 at 07:25

 


Prior to surgery: Gleason T2 6 pirads4 PSA:5.6


post surgery: Gleason 7 (3+4) T2c PSA <0.006


It’s quite a journey. I don’t have a single regret over having a retzius sparing RARP with neurosafe. Choosing a high volume surgeon and top rated hospital I found helped mitigate a lot of concerns. 


if I did it again I would have done it earlier as best to remove cancer as soon as possible in my view. Cancer can spread at any time…that’s the simple pathology of the disease although less likely in early stages. I whip it out when low grade rather than roll the dice waiting for potential prostate capsule breaches. Biopsy can also setup an environment for mets and hopefully in a few years tests and scans will reduce their need.


i looked at focal therapies extensively but wasn’t suitable as my disease was in all four quadrants of the prostate. PCa tends to be a multifocal and in my case this was reinforced by histology which picked up smaller medium grade cells which were missed on biopsy (fairly common). I was also mindful that focal therapies tend to just kick the can down the road in any case and would likely end up needing RARP as some point which would be more complex.


What have a learnt from this journey? Maybe us guys should be offered a baselining PSA test when around 40. Get a second opinion and find a verified high volume surgeon who is regarded as outstanding in their sphere and pioneers the field.


 

Edited by member 22 May 2024 at 14:23  | Reason: Not specified

User
Posted 22 May 2024 at 10:58
Hello Friend, thank you very much for your response… it is very helpful.

Looking at your data and age, it is a very similar case to mine.

I understand your reasoning perfectly, they are very logical.
I am from Spain and I do not know any surgeon who operates
with the Retzius and Neurosafe technique therefore it is a limitation.

I have consulted several specialists (some in favor of AS and others in favor of RARP
and read countless articles and videos on the internet about Gleason 6.
of which it seems that its metastatic capacity is very low or non-existent.

Unfortunately, both the MRI and the biopsy are a true reflection of reality but not necessarily reality.

Unfortunately we can only know this 100% when we remove the prostate (with the side effects that entails)
and it is analyzed in its entirety by the pathologist.

Delaying the timing of treatment is a game of craps in exchange for gaining maximum quality of life
time, but it is also a risk of undergoing theoretically unnecessary surgery.
at Gleason 6 (according to the recommendations of the European and American Clinical Guidelines),
which would be overtreatment.

From what I see in your case, the biopsy was a G6 and post-surgery it confirmed G7
and multiple foci, therefore a posteriori your decision was correct, and your surgery fortunately
went well without side effects, therefore the objective of being cured without aftermath.

B.R.


Originally Posted by: Online Community Member


 


Prior to surgery: Gleason 6 T2 pirads4 PSA:5.6


post surgery: Gleason 7 (3+4) T2c PSA <0.006


It’s quite a journey. I don’t have a single regret over having a retzius sparing RARP with neurosafe. Choosing a high volume surgeon and top rated hospital I found helped mitigate a lot of concerns. 


if I did it again I would have done it earlier as best to remove cancer as soon as possible in my view. Cancer can spread at any time…that’s the simple pathology of the disease although less likely in early stages. I whip it out when low grade rather than roll the dice waiting for potential prostate capsule breaches. Biopsy can also setup an environment for mets and hopefully in a few years tests and scans will reduce their need.


i looked at focal therapies extensively but wasn’t suitable as my disease was in all four quadrants of the prostate. PCa tends to be a multifocal and in my case this was reinforced by histology which picked up smaller medium grade cells which were missed on biopsy (fairly common). I was also mindful that focal therapies tend to just kick the can down the road in any case and would likely end up needing RARP as some point which would be more complex.


What have a learnt from this journey? Maybe us guys should be offered a baselining PSA test when around 40. Get a second opinion and find a verified high volume surgeon who is regarded as outstanding in their sphere and pioneers the field.


 


Edited by member 22 May 2024 at 11:25  | Reason: Not specified

User
Posted 22 May 2024 at 11:22

Originally Posted by: Online Community Member
i looked at focal therapies extensively but wasn’t suitable as my disease was in all four quadrants of the prostate.


Hello again mate


If cancer was detected in all four quadrants of your prostate you were T2c. 


NICE used to class T2c disease, no matter what the grade or volume as high risk and not suitable for AS.


However CPG did away with T2 sub grades and put T2a, T2b and T2c,  all as T2. NICE when adopting CPG, then suddenly, overnight, changed  the old T2c to low risk, suitable for AS.


I found this totally mystifying, especially as research has indicated that T2c disease, being bilateral disease, is much less likely to be the predominant factor, more significant than PSA levels or Gleason score, in AS failure.


Here's a conversation on the subject, which contains links to the aforementioned statements.


https://community.prostatecanceruk.org/posts/t29997-T2c-disease-and-active-surveillance


 

Edited by member 22 May 2024 at 11:56  | Reason: Additional text

User
Posted 22 May 2024 at 11:28
Too not clear if he knew about the involvement of the 4 quadrants before the surgery
(because that already directly excludes it for AS).

Originally Posted by: Online Community Member


Originally Posted by: Online Community Member
i looked at focal therapies extensively but wasn’t suitable as my disease was in all four quadrants of the prostate.


Hello again mate


If cancer was detected in all four quadrants of your prostate you were T2c. 


NICE used to class T2c disease, no matter what the grade or volume as high risk and not suitable for AS.


However CPG did away with T2 sub grades and put T2a, T2b and T2c,  all as T2. NICE when adopting CPG, then suddenly, overnight, changed  the old T2c to low risk, suitable for AS.


I found this totally mystifying, especially as research has indicated that T2c disease, being bilateral disease, is much less likely to be the predominant factor, more significant than PSa levels or Gleason score, in AS failure.


Here's a conversation on the subject. Which contain links to the aforementioned statements.


User
Posted 22 May 2024 at 14:29

@quique


Good to hear from you.


Indeed there are striking parallels. 


I think my prof mentioned in ~44%  cases the cancer type is usually upgrades. In my case he postulated this would be ~60%. Knowing this pushed me to surgery as I had a hunch time was of the essence.


Its a difficult journey to say the least. I hope all the information helps like it did me back in 2019 as this community is fantastic.


btw if you go down the surgical I'm more than happy to ask my prof if he knows surgeons in your locations that use retzius sparing and/or neuroSAFE as I beleive he does the surgical training/education circuit all across EU/US/Asia.


 


 

Edited by member 22 May 2024 at 14:39  | Reason: Not specified

User
Posted 22 May 2024 at 14:37

@Adrian56 Totally agree. Its what set off alarm bells....after London MDT review two options were recommended....AS or RARP. My ex is a researcher in this field so our pillow talk used to be cell pathology, angiogenesis and cribriform cell structures :D


Knowing my PCa was at least T2c I engaged for a second opinion with the Prof Whocannotbenamedonhere as thats seemed like the minimum due diligence. The prof mentioned there was a ~60% chance there would be cribriform gland cells (>=grade 4) on final histology and he was spot on. Acting fast was prudent it would seem as the Prof had to resect additional tissue around the bladder neck and the cancer was extremely close to breaking out of the prostatic capsule.


I count my lucky starts I didnt defer for a couple of months over the xmas period which would have taken me into the covid crisis.


Happy days thus far....


 

User
Posted 22 May 2024 at 14:42

Hello yes please ask him for this surgeons in spain.


Well, most here say that the surgery is quite bearable and with little post-surgery pain,
Some even say that it was worse to wear the urinary catheter for 2 weeks.
So far it is the most difficult decision of my life because I have a lot at stake.
In my case on paper, only unilateral lesion, so the balance must tip according to the reliability
we give to the MRI/biopsy

B.R.

User
Posted 22 May 2024 at 14:52
Yes positive cores in the 4 quadrants = T2c and a cribiform histology (even being Gleason 6)
not is for AS and radical treatment must be applied.

Originally Posted by: Online Community Member


@Adrian56 Totally agree. Its what set off alarm bells....after London MDT review two options were recommended....AS or RARP. My ex is a researcher in this field so our pillow talk used to be cell pathology, angiogenesis and cribriform cell structures :D


Knowing my PCa was at least T2c I engaged for a second opinion with the Prof Whocannotbenamedonhere as thats seemed like the minimum due diligence. The prof mentioned there was a ~60% chance there would be cribriform gland cells (>=grade 4) on final histology and he was spot on. Acting fast was prudent it would seem as the Prof had to resect additional tissue around the bladder neck and the cancer was extremely close to breaking out of the prostatic capsule.


I count my lucky starts I didnt defer for a couple of months over the xmas period which would have taken me into the covid crisis.


Happy days thus far....


 


User
Posted 22 May 2024 at 15:39

Will ping him an email later today as he's probably in surgery now.


Yes, surgery wasnt anymore involved for me than having tonsils out. Catheter was annoying but you get used to it and the associated management. 


My mind was exploding after diagnosis so know how you feel.


I would find a surgeon who is at least high volume. The general accepted classification for high volume in the UK is >100 RARPs a year. I think my prof was 3-4x this number. 


Retzius sparing is apparantly a more complex approach but it tries to avoid disturbing the nerves which control urinary management. I think fundamentally it means faster continence post surgery. Longer term there isn't much difference I think with conventional (anterior) robotic surgery in terms of continence stats. 


NeuroSAFE is see as a no brainer as it basically means a rapid pathology is done to check if cancer cells are on the anterior of the prostate while the patient in open on the surgical table. In the UK is started to be rolled out on the NHS as add a superb level of near real time visibility and hopefully extra reassurances that no cancer is accidently less behind and nerves removed that could be spared.


A few of asked about best prostate cancer clinics in Europe...apparantly the Martini-Klinik Clinic in Germany is very well regarded if you can't locate a top surgeon closer to home.


 

Edited by member 22 May 2024 at 16:35  | Reason: Not specified

User
Posted 22 May 2024 at 19:30

Originally Posted by: Online Community Member

There are studies that support that the metastatic capacity of 3+3 is close to zero,


This is true; "pure" G3+3 cancer is extremely unlikely to metastasise. The main problem is that a biopsy is a random sampling process, and the fact that only G3 cells were found in the samples extracted from your prostate does not mean that G3 cells are all that's actually there. That's why the important word in "active surveillance" is "active"; it's important to have regular scans and PSA tests. 

Best wishes,


Chris


 

User
Posted 22 May 2024 at 20:56

@quique no luck unfortunately with names of surgeons in Spain. 


if you decide to go abroad for treatment maybe drop me a line let me know.


I think the single port Da Vinci robot is now being used at London Guys Cancer Centre.


Cheers


simon

Edited by member 22 May 2024 at 21:11  | Reason: Not specified

User
Posted 22 May 2024 at 21:39
Hello Chris, I completely agree.
Unfortunately, diagnostic tests do not have 100% reliability.
In my case, 5 shots have been taken on the suspicious lesion
in which 3 of them say that there is G3+3 and 2 of them say that there is nothing malignant.
In the rest of the prostate, 9 samples have been taken because there are
no visible lesions on the MRI.
In this particular case, do we remove the prostate now or do we wait to find a G7 or greater?
That is the question

Originally Posted by: Online Community Member


Originally Posted by: Online Community Member

There are studies that support that the metastatic capacity of 3+3 is close to zero,


This is true; "pure" G3+3 cancer is extremely unlikely to metastasise. The main problem is that a biopsy is a random sampling process, and the fact that only G3 cells were found in the samples extracted from your prostate does not mean that G3 cells are all that's actually there. That's why the important word in "active surveillance" is "active"; it's important to have regular scans and PSA tests. 

Best wishes,


Chris


 


User
Posted 04 Jun 2024 at 15:02

Hello again, reviewing my MRI reports I have been able to read that my gleason 6 lesion reaches the prostatic margin... but there is no deformity of the surrounding fat or evidence of extraprostatic extension...
It is surprising that the urological clinical guidelines and inclusion criteria in AS do not take this into account as a critical element when making an accelerated decision about radical treatment or surveillance.


B.R.

Edited by member 04 Jun 2024 at 15:29  | Reason: Not specified

User
Posted 12 Jun 2024 at 21:11
hello i have new PSA result today (5.85 ng/ml) from AS and Gleason 6. 10x11 milimeters. Pirads 4. 52 yrs old men.

30/05/2022: 4.14 ng/ml
25/09/2023: 5.33 ng/ml
12/06/2024: 5.85 ng/ml

PSA rising 0.5 ng/ml in 8 months. Next week i have appointment with the urologist.
I have a bad body and my nerves are stuck in my stomach and I want to cry. Big s*** all this.

B.R.

User
Posted 13 Jun 2024 at 00:26
Good luck with your urologist, hopefully he will help you come to the right decision for you.
User
Posted 13 Jun 2024 at 10:20

Hi 


I have followed your thoughts about the the best choice to make and after affects.I was PSA 2.19 Gleason 3+4=7


at the age of 70 with 5 cores out of 20 positive and was offered Robotic surgery or Brachytherapy and took Brachytherapy as i felt that the side affects may be better.


I am 8 years on in September and think i have had a very good result with no real side affects.


There are no guarantees in any option but if you do go for AS please keep on top of it as a few on here left it to long before making a decision and regretted it.


If you click on my Avatar you can see my Journey and i am happy to answer any questions about it, but i am no professional so can only give my side.


Good luck. John.

Edited by member 13 Jun 2024 at 10:21  | Reason: Not specified

User
Posted 13 Jun 2024 at 16:16

Originally Posted by: Online Community Member
hello i have new PSA result today (5.85 ng/ml) from AS and Gleason 6. 10x11 milimeters. Pirads 4. 52 yrs old men.

30/05/2022: 4.14 ng/ml
25/09/2023: 5.33 ng/ml
12/06/2024: 5.85 ng/ml

PSA rising 0.5 ng/ml in 8 months. Next week i have appointment with the urologist.
I have a bad body and my nerves are stuck in my stomach and I want to cry. Big s*** all this.

B.R.


That demonstrates that the cancer is not developing very fast - personally I wouldn’t be concerned about that ATM. However, at sometime development will speed up and you’ll need to make a decision. Have they suggested HT to slow down the development?

User
Posted 18 Jun 2024 at 17:26

Hello for now only AS is recommended.


 

User
Posted 22 Jun 2024 at 11:50

I was diagnosed gleason 6 about 3 weeks ago. Prior to my diagnosis I had pretty much decided on AS, if I was Gleason 6. On a fact finding visit to the Radiotherapy Team this week I was told a mistake had been made and I was actually Gleason 7 (3+4), which was (another) shock. However, I was pleasantly surprised when the most likely side effects (for my personal situation) were properly explained. I have BPH (66cc) and psa 5.5, so 3 months hormone treatment followed by 4 weeks IMRT/IGRT, 2 more months hormone treatment has been suggested. I'm weighing things up, but this potential exit strategy from AS has made me more relaxed and less anxious. Based on my experience alone, I'd suggest a chat about RT with a professional. I also have a prearranged meeting with a surgeon next week to discuss removal and staying on AS. Trying to keep an open mind till then, but as I say I felt much better after talking to the Radiotherapy Team.

User
Posted 22 Jun 2024 at 13:08
Just remember that the urologists almost always push for RP surgery and the oncologists almost always push for RT. It's the nature of the beast. The bottom line is that in most cases the results are the same - ie curative - but individual cases may respond better to one or the other treatments.
I found it hard to get a truly unbiased opinion as neither seem to communicate with each other and they each only fully understand their own speciality.
User
Posted 25 Jun 2024 at 10:14
A curious case just happened to me now...
In addition to the prostate I am on a follow-up program to monitor a pelvic cyst that requires annual pelvic MRIs.
In the MRI report from 2 weeks ago, the radiologist talks about the prostate as well and compares it with the results from 1 year ago.

Well, the surprise is that it says that I have triangular morphology lesions in both prostate lobes, compatible with prostatitis changes and that remain stable compared to the MRI from a year ago.

Between both pelvic MRIs, a multiparametric MRI in October 2023 was performed in another hospital due to a rise in PSA, which only saw a 10x11 millimeters (square) unique pseudonodular lesion in the left peripheral lobe.

Therefore... in different hospitals, with different radiologists, with different scanners, you see different things... and now what...?

This is crazy!!
User
Posted 30 Sep 2024 at 20:15

Hello again i have bad news... today i get my last psa result and is 35.80 mg/ml.


30/05/2022: 4.14 ng/ml
25/09/2023: 5.33 ng/ml
12/06/2024: 5.85 ng/ml


27/09/2024: 35.80 ng/ml


I am in Shock. To say that at the beginning of August for 2 weeks I had somewhat dark semen and I feel some slight discomfort in the perineal area. At the beginning of August my semen was somewhat dark for 2 weeks and then it returned to normal and for a few days now the semen has had a somewhat yellowish color. :(


What do you think of this sharp increase in the PSA level in just 3 months and diagnosed with Gleason 6 on active surveillance?


Thank u


 

 

Edited by member 30 Sep 2024 at 20:26  | Reason: Not specified

User
Posted 30 Sep 2024 at 22:49

Such a rapid rise could be an infection especially with the semen symptoms. It is very rare for prostate cancer to change so rapidly.

Dave

 
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