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Finished SABR

User
Posted 16 Dec 2021 at 06:58

Had SABR to three areas. My left 9yh rib, my hip ( both done at Preston ) and T4 on my spine, done at the Christie's.

I have an appointment with my Oncologist at Preston on the 17th Jan.

The Oncologist from Christie's rang yesterday ( 6 weeks since SABR to spine complete ) to say they were happy with the way the treatment went......I was really pleased to hear that.

Then the bombshell, just before the treatment to my spine, Christie's did a CT and MRI scans.

The MRI shows an area of concern on mt T1........they do not know if it is another site of cancer or nothing to worry about...........have to wait to see what my PSA is doing at my Jan appointment with my own Oncologist......not the best Christmas present,

I asked if it is cancer, could it be treated with more SABR, but told NHS only fund up to 3 areas.

He did say it may be possible to treat it with normal RT.

Does anybody know if it is cancer, could i get it treated with SABR privately? If so where and roughly how much?

Or is it likely to be the HT route ?

 

Shaun

User
Posted 16 Dec 2021 at 11:04
I can't get my head round this. You were told in July that the cancer was back and had gone to your bones, they have done SABR but you didn't go back onto HT immediately?
"Life can only be understood backwards; but it must be lived forwards." Soren Kierkegaard

User
Posted 14 Jun 2022 at 17:43

Hi Shaun, Obviously not good that PSA is going up, but it has bobbed up and down for you in the past so all is not lost. It may be possible they can find another area to SABR, but if not I guess you can assume HT is the next treatment.

I think in the light of Chris J's inspiring thread, I would be considering how long I could go before taking HT.

It really would be a question of what you want from life and what risks are you happy to take.

Dave

User
Posted 29 Jun 2022 at 18:10

Sorry to see your PSA has risen and you have active bone mets Shaun. Hopefully the Zoladex will knock it on the head.

Ido4

User
Posted 17 Aug 2022 at 17:39

Great news Shaun, keep going mate.

User
Posted 18 Aug 2022 at 00:37
If the other sites were sorted by SABR I would try for another shot what have you got to lose?
User
Posted 23 Aug 2022 at 08:02
Until covid arrived, apalutimide was only available to hormone dependant men as part of a trial - it was only approved for castrate resistant PCa. This is possibly the only silver lining of the pandemic - you are being given the most recent drug available at a staging that wouldn't have been approved for years yet. It is hard to separate out the side effects of the apa from those of the zoladex.

Trials may not be the best thing for you right now as they may result in you not getting the apalutimide.

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

User
Posted 23 Aug 2022 at 14:41

Hello Shaun

Good luck with your treatment, keep positive and fighting.

I've been on Apalutamide and Zolodex for 20 months, the only major side effect for me is fatigue, especially in the afternoons, and the gift that keeps on giving ED !  I try and go swimming most days and find that helps.

My initial PSA was 383,but it has been untraceable for over 15 months.

 

Edited by member 23 Aug 2022 at 14:43  | Reason: Last line.

User
Posted 23 Aug 2022 at 16:23
We used to have a member called Old Al (he was 51 I think when I joined) who was initially so fatigued that he was in a wheelchair. He was involved in some research done by PCUK and took up swimming which ultimately got him out of his wheelchair and walking again. Phone the PCUK nurses and ask about their fatigue research findings - they may have lots of ideas and advice that you haven't thought of.
"Life can only be understood backwards; but it must be lived forwards." Soren Kierkegaard

User
Posted 18 Oct 2022 at 06:16
Was the sabr done on the NHS in the end?
User
Posted 19 Oct 2022 at 12:27

Hi Shaun

It's great to hear good news when treatment is working and PSA dropping,let's hope this continues for you had my latest bloodtest yesterday will hear the results over the phone tomorrow,fingers crossed.

Fight the fight allπŸ’ͺ 

User
Posted 19 Mar 2023 at 08:40

Another good month.

PSA fallen again from 0.2 down to 0.12.

that’s after 9 months on zoladex +7 months on Appalutamide …PSA was 9.6πŸ˜ƒ

shaun

User
Posted 19 Mar 2023 at 09:28

Hi shaun

Great πŸ‘ news about your psa drop,long may it continue,I've had a tad rise in the last couple of months but still low at 1.1 have CT scan booked in a few weeks so fingers crossed 🀞 on that one.

Regards Phil 

User
Posted 08 Dec 2023 at 15:29
Latest PSA down to 0.05

Really pleased with that.

Told the nurse from the Appalutamide company I had achy joints ( known side effect of Appalutamide ), she said to try Devils claw .

I did and noticed a big difference after just two days

User
Posted 09 Dec 2023 at 09:34
Great PSA result Shaun, keep going buddy.
User
Posted 09 Dec 2023 at 10:39

Hi Shaun

That's great news with the PSA long may it continue.

Regards Phil 

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User
Posted 16 Dec 2021 at 09:52

 I don't know anything about private treatment. I do know Christie's have a private wing so I think you should start your search there.

I hope the T1 is nothing. I guess I have to agree with the NHS, they can't afford to play whack-a-mole more than three times.

Dave

User
Posted 16 Dec 2021 at 11:04
I can't get my head round this. You were told in July that the cancer was back and had gone to your bones, they have done SABR but you didn't go back onto HT immediately?
"Life can only be understood backwards; but it must be lived forwards." Soren Kierkegaard

User
Posted 16 Dec 2021 at 12:46

Hi Lyn…. No not on HT…. The oncologist mentioned me going on to HT to wait till Preston were in a position to offer SABR to the spine….. they were only able to do SABR to my rib and hip that’s when she said she would refer me to Christie’s for my spine.

The referral letter to the Christie’s say the SABR is to try and delay the start of HT.

I am expecting her to put me on it in Jan

 

Shaun

Edited by member 16 Dec 2021 at 12:51  | Reason: Not specified

User
Posted 16 Dec 2021 at 13:23
Ah okay - if the new hotspot turns out to be cancer, palliative RT will be just as useful as SABR ... I am not sure that SABR would offer enough of a benefit to be worth paying for.
"Life can only be understood backwards; but it must be lived forwards." Soren Kierkegaard

User
Posted 18 Dec 2021 at 12:04

Hi

i had SABR a few years ago ( two to the pelvic area and one to the 4th left rib) which seems to have worked ok.

i was also told that 3 areas of treatment were the maximum allowed due to financial constraints, so when it showed in my right rib I had to have chemo to sorted it out and I no longer have it in my bones,but after chemo it then appeared in my lymph nodes.

i don't know if they have warned you but SABR to the rib can sometimes result in a fracture of the treated rib many months after, which happened to me so be aware of this.

All the best

Roy

Edited by member 18 Dec 2021 at 12:05  | Reason: Not specified

User
Posted 11 Jan 2022 at 12:16
Just a quick update.

I have had my PSA done ready for my appointment with my oncologist next Monday.

!0 weeks ago my PSA was 9.5, it has now gone down to 8.2.

Feeling really pleased with that, just have to wait and see what the oncologist says and to see what she thinks about the " area of concern " Christie's mentioned on my T1......

Really hoping that this will keep me away from HT for a while longer.

Shaun

User
Posted 11 Jan 2022 at 23:31

Going down is always good.

Dave

User
Posted 19 Jan 2022 at 12:50

Hi, had an appointment with the Oncologist on Monday…..

she said while my PSA is stable…. It’s down from 9.5 to 8.2 after my SABR treatment….. she is not rushing towards starting HT yet…… happy with that.

Because of the comment from Christie’s about area of concern lower down on my spine, she has booked another MRI and  a bone scan….. fingers crossed it turns out to be nothing……. Doubt it with my luck though….

so all in all quite happy with that appointment .

Shaun

User
Posted 26 Jan 2022 at 17:52

I now have metastases in my left side periaortic nodes and possibly in my C3 spinal process after being in remission for 10 years. Would this qualify for SABR treatment on the NHS?

At the moment I am responding well to Zoladex.

User
Posted 26 Jan 2022 at 23:18

They will treat up to 3 spots I believe, but is will also depend on having good access to the spot without something critical being too close, and being able to plan paths without tissues exceeding max lifetime dose if you've previously had RT.

You my have to push to get it though, and it may mean being referred to somewhere else that does it.

User
Posted 15 Mar 2022 at 17:35

Bit of good news

my bone scan came back clear

my PSA has gone down a bit again, down from 8.2 to 7.8 and that drop was in 2 months.

had a scan with contrast to, Thorax, abdomen and pelvic region…

I see the oncologist next Monday for results if that….

hopefully she still won’t put me back on HTπŸ˜ƒ

User
Posted 02 May 2022 at 15:07

Update.

saw the oncologist and my PSA has gone down again….. no treatment needed at present ….. next PSA in 2 months…

I’ll take that for now.πŸ˜ƒ

User
Posted 14 Jun 2022 at 16:39

Well, just had my latest PSA result… it’s started going back up… 3 months ago it was 7.8……. July of 2021, it had got up to 9.6…..

had 3 areas treated with SABR and it fell to 7.8.

it’s now back to 9.6 .

I see my oncologist next Monday so I’m expecting to be back on the HT.

Jan 2016 I was first diagnosed so I suppose I have had a good run.

 

Shaun

User
Posted 14 Jun 2022 at 17:43

Hi Shaun, Obviously not good that PSA is going up, but it has bobbed up and down for you in the past so all is not lost. It may be possible they can find another area to SABR, but if not I guess you can assume HT is the next treatment.

I think in the light of Chris J's inspiring thread, I would be considering how long I could go before taking HT.

It really would be a question of what you want from life and what risks are you happy to take.

Dave

User
Posted 29 Jun 2022 at 09:26

Saw my oncologist on the 20th June..

my PSA had gone up from 7.8 to 9.6.

Thats where it was before SABR to 3 areas that finished Oct 2021.

At that time Christie’s said there was an area of concern on my lower spine, my oncologist had a bone scan done in Mar and was happy with the result and my PSA going down.

when I saw her this time ( Monday )even though my PSA had risen she said she wasn’t in any hurry to start HT as it was only a small rise. She thought it best to have another bone scan and an MRI.

3 hours after leaving her office I was offered a cancellation for my bone scan the next day ( Tuesday ). The following day I got a call asking me to go back and see the oncologist on the following Monday ( got a bad feeling about it ).

She tells us that the area of concern mentioned by Christie’s is now active and thinks it’s time to go back on Zoladex.

We asked about a fourth SABR , saying we were willing to pay private if we had to.

She was willing to ask about it at the next MDT and tell me the follow week. She then went in to say like last time ( if the MDT agreed , it would be 3-4 months to get a psma pet test done again and a bit more time before treatment started. In her opinion that would leave another 4-5 month of the active met on my spine spreading even more cancer around . She said in her heart she did not think it would change things and she honestly felt now was the time to try and put the cancer to sleep as she called it.

Reluctantly I agreed as I trust her judgement and she has thrown the kitchen sink at my cancer over the last 6.5 years. 
so I started taking Bicaltamide before my first Zoladex injection.

I was then asked to take part in a genetic testing trial so I agreed…. Only had to give a saliva sample… was lucky as the trial closes on the 30th.

At the minute I’m looking to see if there are any other trials I could get on.

Bit worried about the Zoladex , as last time it took the 2.5 years I was on it to get it from 24.6 yo 0.03 

Shaun

 

User
Posted 29 Jun 2022 at 18:10

Sorry to see your PSA has risen and you have active bone mets Shaun. Hopefully the Zoladex will knock it on the head.

Ido4

User
Posted 16 Aug 2022 at 21:50

Happy days.

6 weeks after my first Zoladex injection , my PSA has fallen from 9.6 to 2.1.

I see my oncologist next week

 

shaun

User
Posted 17 Aug 2022 at 17:39

Great news Shaun, keep going mate.

User
Posted 18 Aug 2022 at 00:37
If the other sites were sorted by SABR I would try for another shot what have you got to lose?
 
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