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Template Biopsy Results Thursday

User
Posted 21 Apr 2015 at 17:46
After many months on this forum it is "D-day" for my lovely Husband this Thursday. He had his template biopsy last Thu so we have an appointment with his Urologist to get the results, he first noticed symptoms last May but being a typical man didn't tell me until mid October. He is 46 and his PSA's have been 3.82 in Oct and 3.5 in Feb, he did have an MRI in which was indeterminate enlarged prostate with some middle lobe. His other symptoms are lower back pain and thigh pain as well as some ED which I do think is unusual as I have not read much about men having ED until after any op or treatment? Anyway it has been a very long wait for an answer to all of this so I do hope if there is anything it is low grade and something can be done, if nothing is found and the PSA is still high what will they do? Will they just keep monitoring every six months? Does anybody have suggestions of what to ask with either scenario? I will of course be the secretary and take a notebook with me!

Thanks for listening,

Trish x

User
Posted 22 Apr 2015 at 09:13

Sorry, Trish, i can't really foresee how your situation will develop. Until you know either was the results of the biopsy. Let's hope it's negative and your hubby can be treated for an enlarged prostate. PSA testing will probably be 6 monthly, you may wish to ask for 3 monthly, and he could have an op to reduce or be given tablets.

If positive, you will want to know the Gleason scores, and in particular, whether any cancer has escaped the prostate. and the treatment options. You may also be given N and M scores which measure any escape to the lymph nodes and/or further.

Good luck with the diagnosos.

Paul

Stay Calm And Carry On.
User
Posted 22 Apr 2015 at 16:52

Hi Trish,

Good luck for tomorrow, I will be thinking of you.

BFN

Julie X

NEVER LAUGH AT A LIVE DRAGON
User
Posted 22 Apr 2015 at 19:08
Trish

We will be in a similar situation to you in a couple of weeks when all of my hubby's results are in, sending you both good luck wishes for tomorrow.

Maureen x

"You're braver than you believe, stronger than you seem and smarter than you think." A A Milne
User
Posted 22 Apr 2015 at 20:51

Hi Trish

It is unusual for a man to have a template biopsy before a TRUS biopsy - did your man have a TRUS first? The reasons it is unusual is because a TRUS is cheaper and a template requires the patient to have a general anaesthetic with possible extra side effects.

However the Template biopsy is far more accurate so it's good that he has had one as it will be a much surer way of detecting any cancer, if present, and the true extent of any cancer. It will also provide a better assessment of the actual Gleason score.

There is a good explanation of the Template biopsy on a downloadable pdf. If you Google  'Why choose a template biopsy vs TRUS Essex urology' the site should come top of your search. Click on the link then click 'OPEN' to download the pdf.

Often a Template biopsy gives a higher Gleason than a TRUS as it samples much more of the prostate in greater detail and is much more likely to get nearer to the centre of any cancerous cells than the TRUS. Not always though as I have had both and there was no difference between the two in my case.

Good luck tomorrow - let us know how you both get on.

dl

Edited by member 22 Apr 2015 at 20:53  | Reason: Not specified

User
Posted 22 Apr 2015 at 23:28
Thanks DL and Maureen,

I think the reason he is having a Template Biopsy is because I am lucky enough to have BUPA paid by my work for the whole family, you are right about a more accurate result so if there is anything they are likely to find it.

Better try to get some sleep, big day tomorrow and thanks so much for your kind wishes - I would be a bit lost without this forum.

Trish

User
Posted 23 Apr 2015 at 21:53

Hi Trish,

So your results are in and the bad news is yes it is the big C but the good news you are in the cure camp a bit of a bitter sweet moment.  I understand how you are feeling tonight but at least now you have answers and time to plan and talk over your next steps. Trevor was also estranged from his Dad and had no contact since Trevor was 12 years old, we have since his diagnosis found out that he had 2 half brothers  that have sadly died of pca and several half brothers. So we also understand the complexities of telling estranged family members. 

BFN

Julie X

Edited by member 23 Apr 2015 at 22:00  | Reason: Not specified

NEVER LAUGH AT A LIVE DRAGON
User
Posted 23 Apr 2015 at 22:04

Hi Trish, sorry to see you on here for obvious reasons. It is a shock when first diagnosed but at least you have options. Don't rush into any decisions, listen to all the options, take notes as you forget things when you leave the oncologists office. Then make his decision based on what he thinks will be the best course of action for him and what he thinks he will cope with the best. My first thought was "Surgery, just cut the thing out".  It took me 2 or 3 months to decide on Brachytherapy and I changed my mind several times along the way. I eventually had the procedure in January this year so it is still early days.

Good luck with whatever treatment he decides on.

User
Posted 23 Apr 2015 at 23:44

Hi Trish

Sorry you did not get the results you hoped for, but my advice would be to stay positive, choose your treatment carefully, and be supportive. Good luck in whatever you decide.

Paul

Stay Calm And Carry On.
User
Posted 24 Apr 2015 at 16:37
Trish I am so sorry it has turned out this way. Big decisions to be made now so talk loads discuss all the options and if you need to ask questions here there will always be someone who can help with words of wisdom.

Looks like you and Lonners are going to be traveling a very similar path right now.

Thinking of you

Xx

Mo

User
Posted 24 Apr 2015 at 23:55
Trish I assure you I am not so much wise just caring and I hope able to bring perspective

Xx

MO

User
Posted 01 Jun 2015 at 16:53
Dear All,

Thanks for all your input but my post was written about 6 weeks ago and the decision has been made to have Da Vinci, our Oncologist advised against Brachytherapy because of Stuart very poor urine flow as he would have had to have TURP first and the Brachytherapy after 6 months. To be honest Stuart did not want Brachytherapy anyway so made the decision to go for Da Vinci easier. We have done all the research and for him he feels this the way to go. His OP is 9th July.

Thanks again

Trish

User
Posted 01 Jun 2015 at 18:08

Well done Trish

Originally Posted by: Online Community Member
Dear All,

Thanks for all your input but my post was written about 6 weeks ago and the decision has been made to have Da Vinci, our Oncologist advised against Brachytherapy because of Stuart very poor urine flow as he would have had to have TURP first and the Brachytherapy after 6 months. To be honest Stuart did not want Brachytherapy anyway so made the decision to go for Da Vinci easier. We have done all the research and for him he feels this the way to go. His OP is 9th July.

Thanks again
Trish

Show Most Thanked Posts
User
Posted 22 Apr 2015 at 09:13

Sorry, Trish, i can't really foresee how your situation will develop. Until you know either was the results of the biopsy. Let's hope it's negative and your hubby can be treated for an enlarged prostate. PSA testing will probably be 6 monthly, you may wish to ask for 3 monthly, and he could have an op to reduce or be given tablets.

If positive, you will want to know the Gleason scores, and in particular, whether any cancer has escaped the prostate. and the treatment options. You may also be given N and M scores which measure any escape to the lymph nodes and/or further.

Good luck with the diagnosos.

Paul

Stay Calm And Carry On.
User
Posted 22 Apr 2015 at 15:56
Thanks Paul,

Will post again when he has the outcome.

Trish

User
Posted 22 Apr 2015 at 16:52

Hi Trish,

Good luck for tomorrow, I will be thinking of you.

BFN

Julie X

NEVER LAUGH AT A LIVE DRAGON
User
Posted 22 Apr 2015 at 19:08
Trish

We will be in a similar situation to you in a couple of weeks when all of my hubby's results are in, sending you both good luck wishes for tomorrow.

Maureen x

"You're braver than you believe, stronger than you seem and smarter than you think." A A Milne
User
Posted 22 Apr 2015 at 20:51

Hi Trish

It is unusual for a man to have a template biopsy before a TRUS biopsy - did your man have a TRUS first? The reasons it is unusual is because a TRUS is cheaper and a template requires the patient to have a general anaesthetic with possible extra side effects.

However the Template biopsy is far more accurate so it's good that he has had one as it will be a much surer way of detecting any cancer, if present, and the true extent of any cancer. It will also provide a better assessment of the actual Gleason score.

There is a good explanation of the Template biopsy on a downloadable pdf. If you Google  'Why choose a template biopsy vs TRUS Essex urology' the site should come top of your search. Click on the link then click 'OPEN' to download the pdf.

Often a Template biopsy gives a higher Gleason than a TRUS as it samples much more of the prostate in greater detail and is much more likely to get nearer to the centre of any cancerous cells than the TRUS. Not always though as I have had both and there was no difference between the two in my case.

Good luck tomorrow - let us know how you both get on.

dl

Edited by member 22 Apr 2015 at 20:53  | Reason: Not specified

User
Posted 22 Apr 2015 at 23:28
Thanks DL and Maureen,

I think the reason he is having a Template Biopsy is because I am lucky enough to have BUPA paid by my work for the whole family, you are right about a more accurate result so if there is anything they are likely to find it.

Better try to get some sleep, big day tomorrow and thanks so much for your kind wishes - I would be a bit lost without this forum.

Trish

User
Posted 23 Apr 2015 at 21:31
Results came in today T2a-c Gleeson 6 3 +3, 1 8mm tumour and the rest what he described as spots of cancer. Stuart had already had an MRI scan and there was a spot that they were slightly concerned about so that must have been the 8mm Tumour. The urologist had said a few options, watchful waiting, removal by Da Vinci or Brachytherapy. He had now referred us to an Oncologist to discuss Brachytherapy and a Urologist to discuss Prostate removal, we have now got to look into both and see what is best for Stuart. I have been reading about this since Oct last year when it all started but my husband didn't want to know anything unless he was diagnosed so now here we are, we will have a long weekend reading everything so he then knows/understands all the options and what that entails IE side effects. I wish he knew more as all of this is going to be a big shock to him. I know we have to be positive about everything as so many men have higher gleeson scores etc but still such a shock and our life will be so different from now. My Husband was also estranged from his Dad and his brother told him tonight that his Dad, Uncle and Cousin all had PC so his brother also described symptoms he was having so I told him to have a PSA test , he has promised to make an appointment with doctor tomorrow.

Thanks for listening.

Trish x

User
Posted 23 Apr 2015 at 21:53

Hi Trish,

So your results are in and the bad news is yes it is the big C but the good news you are in the cure camp a bit of a bitter sweet moment.  I understand how you are feeling tonight but at least now you have answers and time to plan and talk over your next steps. Trevor was also estranged from his Dad and had no contact since Trevor was 12 years old, we have since his diagnosis found out that he had 2 half brothers  that have sadly died of pca and several half brothers. So we also understand the complexities of telling estranged family members. 

BFN

Julie X

Edited by member 23 Apr 2015 at 22:00  | Reason: Not specified

NEVER LAUGH AT A LIVE DRAGON
User
Posted 23 Apr 2015 at 22:04

Hi Trish, sorry to see you on here for obvious reasons. It is a shock when first diagnosed but at least you have options. Don't rush into any decisions, listen to all the options, take notes as you forget things when you leave the oncologists office. Then make his decision based on what he thinks will be the best course of action for him and what he thinks he will cope with the best. My first thought was "Surgery, just cut the thing out".  It took me 2 or 3 months to decide on Brachytherapy and I changed my mind several times along the way. I eventually had the procedure in January this year so it is still early days.

Good luck with whatever treatment he decides on.

User
Posted 23 Apr 2015 at 22:41
Hi Julie,

Thanks for your reply, I think he was a bit shocked to find out so many family members had it but he is also fully aware of the percentage of Afro Carribbean Men getting this disease that it was not a "complete shock". I really am hoping that his brother is also ok as his Mum has Lung Cancer and I really don't think she would cope with the news that 2 of her sons have PC.

Hi Lyrical,

As I said before lots to think about but how did you feel after having Brachytherapy procedure? We would like to see what people think of either option.

thanks x

User
Posted 23 Apr 2015 at 23:44

Hi Trish

Sorry you did not get the results you hoped for, but my advice would be to stay positive, choose your treatment carefully, and be supportive. Good luck in whatever you decide.

Paul

Stay Calm And Carry On.
User
Posted 24 Apr 2015 at 16:37
Trish I am so sorry it has turned out this way. Big decisions to be made now so talk loads discuss all the options and if you need to ask questions here there will always be someone who can help with words of wisdom.

Looks like you and Lonners are going to be traveling a very similar path right now.

Thinking of you

Xx

Mo

User
Posted 24 Apr 2015 at 23:46
Thanks Mo,

I always find reading all of your posts such a comfort, you seem like a lovely wise woman. Yes lots of reading and talking over the coming week or two so that Stuart makes a choice that he feels suits him best.

BFN,

Trish xx

User
Posted 24 Apr 2015 at 23:55
Trish I assure you I am not so much wise just caring and I hope able to bring perspective

Xx

MO

User
Posted 31 May 2015 at 23:47

Hi Trish

Your man is facing a dilemma many men with localised prostate cancer on this forum have faced ..... what is the best treatment option for me? I believe the best option is the one that you both want after HAVING HAD THE CHANCE TO CONSIDER ALL OPTIONS and ask all the questions you feel you need to. It's great that your specialist has referred you man to both an urologist (surgeon in my book) and an oncologist. My first specialist was a surgical urologist and he strongly recommended Da Vinci and wasn't keen for me to discuss my situation with an oncologist. One of the first questions I asked him was 'what if I wait for 2 or 3 months before I make my decision .... would it increase the risk of the cancer spreading' .... to which he answered 'it would make no difference at all' in my case (PSA 13.8, Gleeson 3+4, Staging: T1c, N0, M0). For info I was diagnosed last August and had my treatment earlier this month! I agree with Lyrical that all men are different, not only in that it seems every cancer situation has its differences but that the way they want to deal with their cancer and the risks they are willing to take are different. After talking with some folk who have had PCa they said they just wanted to get rid of it as quick as possible (even many of those with localised PCa, what I consider as a low PSA and Gleeson 3+3) and wanted their PSA to fall to as near as possible to zero ASAP. These men always choose prostatectomy and that was the right treatment for them as that's what they wanted for peace of mind.

In the months I had to study the subject I choose brachytherapy as this was the treatment I felt comfortable to have.

Clearly there are men who have all three of the main options for localised PCa, prostatectomy, brachytherapy and EBRT who have had few problems post treatment and there are those that have had nightmare experiences with these treatments and then there are those who have faired somewhere between the two extremes. The latter is going include the majority of men.

As a rule I believe that sites like this tend to have a membership that understandably belong to those that have had a problem with their treatment, are suffering with more advanced stages of the disease or are, like you and hubby, looking for advice after diagnosis. Those who have 'swanned' through their treatment don't tend to need as much support and therefore don't necessarily search for it on sites like this. Some may criticise me for saying so but I genuinely think that is the case although there are those who have had successful and fairly 'painless' treatment who are on this site to kindly support others. I would also like to add that sites like this are invaluable and many posts have helped me no end.

The evidence re. success of all three of the main treatments for localised PSA are similar. The journey reaching that success has reasonably clear statistical differences, rather than individual experiences, which you should consider.

Another thing to take into account regarding personal choices relates to past experiences. As an example, some men diagnosed with PCa have been used to 7 or 8 hours of unbroken sleep every night and the thought of having to pee during the night is horrendous for them. Other men, like me, have been peeing a couple of times very night for many, many years so a long term side affect of treatment of having to get up twice a night to pee, or pee more often in the daytime than most men, is no big deal.

In summery, if it's possible to take time to make the decision ..... have a holiday or long weekend break to get away form the humdrum of 'normal' life and reduce the pressure. Make a decision whilst you are as relaxed as you can be. Ask questions, do your research and search your hearts for your gut feelings on what is right for YOU.

Life will be different now, you can't avoid that ........ but have confidence in yourselves that you can both make the right decision, given time.

Take good care of each other and let us know how you get on.

dl

Originally Posted by: Online Community Member
Results came in today T2a-c Gleeson 6 3 +3, 1 8mm tumour and the rest what he described as spots of cancer. Stuart had already had an MRI scan and there was a spot that they were slightly concerned about so that must have been the 8mm Tumour. The urologist had said a few options, watchful waiting, removal by Da Vinci or Brachytherapy. He had now referred us to an Oncologist to discuss Brachytherapy and a Urologist to discuss Prostate removal, we have now got to look into both and see what is best for Stuart. I have been reading about this since Oct last year when it all started but my husband didn't want to know anything unless he was diagnosed so now here we are, we will have a long weekend reading everything so he then knows/understands all the options and what that entails IE side effects. I wish he knew more as all of this is going to be a big shock to him. I know we have to be positive about everything as so many men have higher gleeson scores etc but still such a shock and our life will be so different from now. My Husband was also estranged from his Dad and his brother told him tonight that his Dad, Uncle and Cousin all had PC so his brother also described symptoms he was having so I told him to have a PSA test , he has promised to make an appointment with doctor tomorrow.

Thanks for listening.

Trish x

Edited by member 01 Jun 2015 at 00:00  | Reason: Not specified

User
Posted 01 Jun 2015 at 01:23

Posted by Devon Lad 

"Another thing to take into account regarding personal choices relates to past experiences. As an example, some men diagnosed with PCa have been used to 7 or 8 hours of unbroken sleep every night and the thought of having to pee during the night is horrendous for them. Other men, like me, have been peeing a couple of times very night for many, many years so a long term side affect of treatment of having to get up twice a night to pee, or pee more often in the daytime than most men, is no big deal."

 

On a brighter note, there are also men like my OH who had coped with broken sleep and multiple loo trips every night since he was 35 - the most stunning and welcome side effect of the treatment was that he could sleep through for the first time in years! That and the fact that he regained a stream rather than a trickle were an unexpected bonus :-)

"Life can only be understood backwards; but it must be lived forwards." Soren Kierkegaard

User
Posted 01 Jun 2015 at 14:44

I agree Lyn but you know as well as I do that the side affects of the various treatments effect men in different ways and different degrees. It is well documented that in the longer term impotence and incontinence complications occur amongst more men who have a prostatectomy than with EBR or brachytherapy although EBR causes more impotence complications than brachytherapy. EBR is associated with more rectal problems than the other two forms of treatment and a downside of brachytherapy can be retention due to the prostate enlarging and 'squeezing' the urethra.

Naturally there are exceptions to the rules but we shouldn't muddy the waters for folk trying to choose a treatment.

In addition to my frequency example there are some men who are not naturally sexually active and these men are more likely not to be too concerned about loosing their erections.

As you know I had a 'limited' TURP myself in March and after the initial couple of weeks my flow rate improved beyond what I can remember beforehand as the 'restriction' was removed. The brachytherapy last month has reversed this trend for the moment. During the day it's like it was before the TURP and worse at night. However these effects are likely to be temporary and in a couple of months should start to return to how it was after the TURP.

dl

Quote:

Posted by Devon Lad 

"Another thing to take into account regarding personal choices relates to past experiences. As an example, some men diagnosed with PCa have been used to 7 or 8 hours of unbroken sleep every night and the thought of having to pee during the night is horrendous for them. Other men, like me, have been peeing a couple of times very night for many, many years so a long term side affect of treatment of having to get up twice a night to pee, or pee more often in the daytime than most men, is no big deal."

 

On a brighter note, there are also men like my OH who had coped with broken sleep and multiple loo trips every night since he was 35 - the most stunning and welcome side effect of the treatment was that he could sleep through for the first time in years! That and the fact that he regained a stream rather than a trickle were an unexpected bonus :-)

Edited by member 01 Jun 2015 at 14:45  | Reason: Not specified

User
Posted 01 Jun 2015 at 15:27

Hi Trish
I had a template at xmas and it was 25 samples. Two showed 3+4 and they were not too concerned. But these biopsies can still get it wrong. I know u have read and replied to my post. , and I wish u all the best. Oncology ASSURED me HT/BRACCHY/EBR was genuinely the way to go for overall success and impact on lifestyle. , and we loved the thought. The template was wrong though , and the oncology route was taken away. Many people on here promote RP , and others think oncology is the way. It's difficult isn't it ! I'm a newbie as u know so I can't really give advice , but I agree with the consensus " pick and don't look back " . All the best Chris

User
Posted 01 Jun 2015 at 16:53
Dear All,

Thanks for all your input but my post was written about 6 weeks ago and the decision has been made to have Da Vinci, our Oncologist advised against Brachytherapy because of Stuart very poor urine flow as he would have had to have TURP first and the Brachytherapy after 6 months. To be honest Stuart did not want Brachytherapy anyway so made the decision to go for Da Vinci easier. We have done all the research and for him he feels this the way to go. His OP is 9th July.

Thanks again

Trish

User
Posted 01 Jun 2015 at 18:08

Well done Trish

Originally Posted by: Online Community Member
Dear All,

Thanks for all your input but my post was written about 6 weeks ago and the decision has been made to have Da Vinci, our Oncologist advised against Brachytherapy because of Stuart very poor urine flow as he would have had to have TURP first and the Brachytherapy after 6 months. To be honest Stuart did not want Brachytherapy anyway so made the decision to go for Da Vinci easier. We have done all the research and for him he feels this the way to go. His OP is 9th July.

Thanks again
Trish

User
Posted 01 Jun 2015 at 18:51

changed my mind - deleted

Edited by member 01 Jun 2015 at 21:17  | Reason: Not specified

"Life can only be understood backwards; but it must be lived forwards." Soren Kierkegaard

 
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