Tulsa Pro - share your experiences

Posted by bjroc @bjroc, Nov 28, 2023

I want to thank all for support on my recent prostate cancer treatment, Tulsa pro. I am very thankful to my wife and my daughter who helped out lots with support. I am thankful to Mayo for finally finding the extent of the problem with a transperineal biopsy. I am also very thankful to Dr Scionti in Sarasota for being a true expert for the Tulsa procedure. Tulsa leaves everything intact except for the prostate cancer tissue plus some tissue as a safety margin near it. It goes nowhere near sphincters and nerves. I was very glad to not have any extra prostatic cancer, or cancer in seminal vesicles, ducts, nerves etc. I did have PSMA scan showing this. We will just have to see if everything works out in the long run cancer wise.

What I had cancer wise
Originally in 2021 I had a small spot seen in transition zone. It got some 3+3 more toward back where they could reach via trans rectal biopsy (done at a local university), but they could not reach the anterior where most of it was in 2021. My 2023 Mayo done transperineal biopsy had one needle at the anterior transition zone with all Gleason 4, it was not a big spot (0.2 mm caught in needle). Keep in mind in 2021 further to back it had just Gleason 3. I am not going to get caught up in Gleason scores, I know what was sampled in past, and though one needle had 4 in the front/top of anterior it was just a tiny spot in this tumor and most toward posterior was not hit here in 2023. There was also a small 3+4 on one side seen now in 2023. My PSA headed up steadily during the 2.75 years on surveillance. My final prostate size before any treatment was 110 cc, and final PSA around 16.

What worked on biopsy, and what did not.
2021: Trans rectal in 2021 biopsy did not sample well, missed most of what is in anterior transition zone and one of my problem areas. But since then, I have had plenty of time to read on things like Tulsa pro, radiation types, and so on. So was glad to have the time.
2023: Mayo Transperineally done biopsy caught the problems.

Some things I learned about MRI
What I learned is that, for me at least, diffusion weighted MRI shows very clearly what docs need to see to treat. Regular contrast enhanced MRI left my doctors not that sure, sometimes even confused. Diffusion weighted MRI to me was crystal clear where things were and what needed to be treated. Only Dr Scionti seemed geared up for diffusion weighted MRI. That includes other places I asked for initial consult, and Mayo that I went to for a while – all geared up for contrast enhanced MRI only really seemed like.

Who does new kinds of treatments.
Mayo is top notch for advanced cancers that have spread, but I learned they are just starting out with other new treatments like Tulsa Pro. I liked Mayo’s proton as a possibility, but they have filled many slots for it, and sometimes it is hard to get through insurance from what they said to me. They also do everything under protocols, they have to develop those for these new treatments of any kind since everyone looks at Mayo. So in some ways they are behind a bit, having to do everything with a protocol instead of just looking out for what is best for one individual patient. Thus, I found I had to call around if I wanted anything new. Some places are better than others seemed like to me at calling places. The best I heard from was Dr Scionti in Sarasota.

Before Tulsa for me
Because the size of my prostate was large, and one needle had all Gl 4, we did bicalutamide and dutasteride for several months. They want that temperature up during Tulsa at the top so while I still met the Tulsa size limits we shrunk things a bit to be sure.

Travel
I had to travel to Sarasota, about a 22 hour drive for me. Found a nice Airbnb down there not too far away. I drove since date of coming back was uncertain. I wanted his office to take catheter out, others might fly and self remove catheter I understand, but I was unsure about that. It is good I rented an Airbnb for more than two weeks is all I can say.

Tulsa procedure
Obviously asleep, seemed to go well. They took out about 2/3 of the prostate tissue with the Tulsa pro. The before and after MRI done while asleep clearly shows the tumors on diffusion weighted MRI, and post procedure MRI with contrast show those same areas treated well and no longer there. Woke up with the bladder spasms a real lot, oxybutynin seemed to really help but it was hard to wake up with Foley catheter and the spasms. Next day the spasms were gone, but it was tough to sit. For ten days with Foley catheter, I watched old Dr Who, movies, and obviously just sleeping. A restful period is the best help, not having to do much was important for me at least. Foley catheter for ten days was no fun but it wasn’t as hard as I imagined perhaps.

Post catheter
Was a bit tough, I still had some inflammation perhaps worse than some get, plus there is scar tissue for up to 6 months, so it was hard to pee. Alpha blocker was a must just to pee. Another couple weeks brings me to now at this writing and it is a lot easier to pee. But it was a hard travel back. I suggest stay in an Airbnb for some time post procedure plus give plenty of time after catheter is out.

Future
We will see if this all worked on the cancer over next year or two, and on after that. Hoping for no recurrence of course.

Interested in more discussions like this? Go to the Prostate Cancer Support Group.

Profile picture for bjroc @bjroc

@solar4ever Unless it is extended out of prostate, do talk to all the focal doctor experts which by the way they can take out most or just about all of the prostate if need be. You can do many options, not just the standard two offered even in small cities in US. You can go for Brachy, Tulsa, Cryo, etc. These are all good options. All those other things people talk about with lots of verbiage are often used to push people to the standard two option, so unless there are really reasons, call around and get as many as possible appointments. Best advice is do it fast as it takes time to get in, you can always delay your procedure if need be, they can do those RP's anytime and anywhere in US. Many times you will have to travel to get the other options, well worth it. Don't bother just with some big name medical center, some big names offer standard two options that are offered in small cities, so don't just go for a big name, go where they are experts in more than two options. However, Mayo is a big name and they have it all, many options available though you have to get to the doctors with the other options so look up doc and ask for ones that do other things. I had Tulsa, and Cryo.

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@bjroc
Ty
This is punishing

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Profile picture for Jeff Marchi @jeffmarc

@solar4ever

You left a lot of information out. I generally feel what I wrote below fits. It was written for somebody 68.

Are you a T2b?

How many cores had 3+4, how many total cores were taken?.

Were any of these things found in the biopsy intraductal, ductal, large cribriform, Seminal vesicle invasion, EPE or ECE. (Extraprostatic extensions extra capsular extensions). They can make the cancer much more aggressive.

I just wrote this to someone else and it applies to you as well

The one thing I’m missing is your T level? Are you a T2c by any chance, since it’s on both sides of the prostate. Not a T3 which is more aggressive.

You could get SBRT. It’s very commonly used and works well. It’s more likely one and done with what appears to be a lower level case. It actually is more recently the preferred method for handling cribriform. In the past, they thought surgery was better but more recent testing has shown that radiation is more effective. Some doctors still want to do surgery.

If you get surgery, make sure to get Retzius sparing surgery which can keep you continent. If you could also have the nerves spared that would make getting an erection more likely. With it on both sides of the prostate, there may be a problem. This has to be discussed with the surgeon.

After SBRT most people can still get an erection. Overtime it usually fades because they have burned the nerves.

In either case erection problems can be resolved. You can use injections to get an erection, Sometimes Cialis or Viagra will work and if not the implant is really popular 90% like it.

It will take a few months to be acclimated after surgery. You may have incontinence issues for a few weeks. You may not be able to get an erection right away.

I think I would probably prefer radiation if I were in your exact situation. If ED Problems eventually come, you can always resolve them.

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@jeffmarc this journey is hard
Looks like six at 3+3
And six at 3+4
And two at benign
All show cribiform (not identified)
Clinical stage t1c

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Profile picture for solar4ever @solar4ever

@jeffmarc this journey is hard
Looks like six at 3+3
And six at 3+4
And two at benign
All show cribiform (not identified)
Clinical stage t1c

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@solar4ever
That’s a lot of cores with something. Definitely looks like surgery or radiation is necessary soon. If you feel that surgery is right for you then go for it. I picked surgery when I was 62 and it gave me 3 1/2 more years before my PSA started rising and I Had salvage radiation.

Did you speak to a radiation oncologist about your situation? Not saying that surgery is wrong, Just that you need to at least look at the other options. Five sessions of SBRT radiation may be enough.

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Oncologist deferred, said I could do surgery or active surveillance for a bit! Didn’t think I was a good candidate for some reason.
This is all very confusing!!

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Profile picture for solar4ever @solar4ever

@jeffmarc this journey is hard
Looks like six at 3+3
And six at 3+4
And two at benign
All show cribiform (not identified)
Clinical stage t1c

Jump to this post

@solar4ever
my first ultrasound biopsy in 2025 also showed all 12 cores with cancer. I was floored. 12 of 12 really? I have heard of very few with 12 of 12. I joked with my wife we should buy lottery tickets. 🤣 Anyway…. All 3+3 except one 3+4 (only 5% of the 4) Psa 4.5. Low decipher of 0.32. Not hereditary. No cribriform or perinureal invasion. Went on Active Surveillance for a year.

Due to some PIRADS of 4 in a second MRI Feb of this year, I had an MRI diffusion weighted biopsy that showed 9 of 12 cores with cancer. One 3+4 but one at 3+5 <5% of the 5). That was a shocker. Perinueral invasion was present. Still no cribriform. Clean PET scan. Second Decipher in the Gleason 8 sample was even lower at a 0.19.

Time for treatment. I chose IMRT/VMAT 28 sessions with Barrigel spacer and gold markers. I had the Prostox test which came back low risk for radiation related sensitivity. I wanted to get all the cancer they could shoot at…including hopefully most microscopic cancer. Didn’t want the risk of incontenence . No ADT due to the low Decipher.

Finished the 28 sessions last week. Some slight burning and frequency of urination but Flomax prescription knocked that down. Some bowel movement changes but overall not too bad.

Now wait for first PSA at
3 mo.

One thing…. If I had to do all over again would have demanded diffusion weighted biopsy the first time. Ultrasound biopsy missed a lot. Not sure why urologist didn’t opt for the most accurate test first. I think because I only had PIRADS 3 during the first MRI. Demand the diffusion weighted biopsy if you didn’t have it.

Stay strong. This is treatable.

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