4th and Last PRRT

I’m a bit late posting about my last peptide receptor radiation therapy (PRRT). Mainly due to there not be much to report! Everything went fine and I only have one blown vein (instead of 5).

The side affects are about the same. Sour stomach and I’m pretty tired. One new issue is I get dizzy when I exert myself (even walking upstairs at home). My blood count was low before this last treatment so I’m guessing they are even lower. I don’t go back to the oncologist until the 22nd. I guess they will check my blood counts then. I’ve been taking B-12 and it helps a little with the fatigue.

Success!
This is what they gave me when I was all finished for the day! Too bad it wasn’t real Champaign!

June 18th was actually my 9th Cancerversary! Hard to believe I’ve had this cancer for 9 years. I may have to dedicate a post just to that.

That’s all for now. I hope you are all well and stay cool if you are caught in the heat wave we’ve been having across certain parts of the country!

3 out of 4

I’m not sure how I feel about round 4. Part of me is wanting to “get er done” and part of me is dreading it. I’m still not sure I’m recovered from round 3 and it’s been over two weeks.

Round 3 went well. They had to use a different supplier for the amino acids as their usual one we out. I think this “brand” was easier on me as I didn’t have a headache or stomach pain the next day. I’m pretty sure what side effects I’m having are from the actual Lutathera (radioactive drug). It makes sense that the affect would be cumulative as they are with most chemo/radiation treatments.

Side Effects

My tummy is still on/off sour. I’m occasionally nauseous. I’m very tired most days but it is getting better.

I hope by round 4 (final) I’ll be feeling 100% (well, as much as I ever feel 100%–my 100% is probably 70% of a truly healthy person).

On another note, Utah has lifted the mask mandate! I’m fully vaccinated but will continue to mask-up where required (some grocery stores, etc.). I will admit to loving it when I can go in somewhere without a mask. I hate them. I know some people will continue to wear them regardless of the mandates. I can understand their point of view but it’s definitely not for me!

I see my oncologist next week. I’m sure it’s a “how are you feeling” and a total waste of time. Blood work will be two weeks after that to see if round 4 is a go. I’m feeling fairly positive that it will be! Its actually gone by really fast.

Until next time…

I’m late with my update…

I realized I never did update my 2nd round of PRRT. That’s mainly because everything went just fine. It was a slightly shorter day (whew). We were done by 2:30pm. The 3rd round is planned for April 29th. I felt ok afterwards. My throat was sore for a few days and my stomach was, again, sour. Fatigue is a little worse but I’m taking pain meds throughout the day so it could be those.

My creatinine has been hovering around 50-53 and it has to stay above 50 or they will not do the next round. My GP took me off Celebrex due to thinking it was affecting my kidneys. Since then, I have been incredibly miserable from cervical neck pain. I am shocked at how much the Celebrex was helping me. I even went back to the pain clinic and had another occipital nerve block, hoping it would help. It hasn’t. The pain doc told me to take more pain pills if I need to. I’m so mad. I had the nerve stimulator implant so that I wouldn’t have to take more and more pain pills. Now I’m in that (slowly sinking) boat anyway.

Oncologist appointment this week. I don’t know if they will do bloodwork. They usually do when I see him. Hopefully, since I’m off the Celebrex, my creatine will be better. I forgot to mention that it has been “below normal” for years…

Stay well, stay safe!

Here’s a cute picture of my dog Sookie. Just for fun.

One down, three to go!

I’m a little late posting an update about my first PRRT treatment. First, I’d like to say it went off without a hitch (or hiccup)!

I was there from 8am until 3pm. Long day but it went by quite fast. My nurse, Jen, was awesome! She checked on me just the right amount. Not too much to be annoying!

When I first arrived, she had me change my clothes. I wore a hospital gown with paper-like shorts under it! Plus paper booties. The don’t like you wearing your own clothes as the radiation might stay in them longer then they like. Next time, I am taking some hospital socks I have and then I’ll just throw them away. The paper booties didn’t want to stay on.

After the change of clothes, she started my two iv’s. One in each arm. They use one just for the Lutathera (radioactive material, which was clear and in a glass bottle like you would see insulin or something).

She then started some anti-nausea meds and an antihistamine (non-drowsy).

Then after about an hour (I think) they started the amino acids, which protect the kidneys since Lutathera likes to accumulate in the kidneys (which isn’t good). I had that infusion for an hour before they brought in the Lutathera. It was very interesting how they administered it. I will try to remember to take a picture next time. They use gravity for the infusion. The bottle was put into another container (probably lead-lined) and a long needle was inserted into the top of the bottle. Then another needle was inserted that went to my saline solution iv bag. The slow release of the saline, into the Lutathera bottle, pushed the drug into my IV. It took about 35-40 minutes. I had two radiation techs plus my nurse in the room with me during this time. They continually checked the radiation levels going out from the bottle and then into my arm. It was pretty cool.

After that finished, it was 3 more hours of amino acids. Then we waited another hour and she gave me my lanreotide shot. They found it’s better to give it the day of Lutathera over waiting until the next day as patients were having some carciniod crisis symptoms the day following Lutathera. Something like that.

I have pictures but haven’t figured out how to insert them! If anyone has a quick tutorial, send it my way!

Until next time. Stay safe out there!

PRRT is the Plan

I had a bad month in October. I just felt like crap. Flushing constantly (or at least it feels like it). I’m still not sure if it’s my hot flashes coming back with a vengeance or flushing. I am getting red/pink now whereas I didn’t before (except my ears would turn purple).

I saw the PA at the cancer clinic and she was so kind and caring. She ordered another Gallium Scan and off I went. I went in this morning to meet with my oncologist and the scan report said mostly the same, some tumors are bigger but have less uptake. I don’t really know what that means. The report did mention a lymph node that is lighting up somewhere by my esophagus. No change from last scan–um, this wasn’t even mentioned in the last scan report. Once again, no effort made by my oncologist to show me the scan. I didn’t even ask.

I decided that I am moving ahead with PRRT. I have no idea how long the process is to get it. I didn’t leave feeling very confident that the clinic really knew what they were doing. I’m not sure why. I know others who go there that have had PRRT. I’ve sent an email to one to ask him how long it took before he actually got it. I didn’t even ask about liver only directed therapy. I had pretty much decided on my own that PRRT was better as a first line treatment. If the veins/arteries feeding the tumors are damaged, from say, liver embolization’s, then the PRRT will not be as effective. I can still do liver directed therapy after PRRT without any damage being done to the veins so…

I also had a cervical nerve stimulator test done for my cervical (neck) pain. It didn’t work as well as I hoped it would but it did help by reducing my pain by about 50% -70%. The doc feels this is enough to go ahead and get the real deal. I have that getting approved and scheduled but I told them I was in no hurry and it didn’t need to happen before the end of the year since my insurance year is July-June. Other patients are trying to get in before their insurance reboots Jan. 1st and I didn’t want to take up an OR spot when I can wait. Aren’t I nice???

I’m hoping I can get the first treatment of PRRT done before the end of the year. They have to time it with my lanreotide shot–or just before my shot is due. They need my tumor receptors to be “hungry” for the radioactive somostatin analog they will be injecting. I’ve heard this treatment described as liquid radiation. I like it.

So this is where I’m at. Waiting…