I did my FIRST Lu-177 infusion on the 23rd of April, 2019. 15 days later on the 8th of May (today), I took a series of blood tests including my serum PSA. The PSA level has risen to 16.92 from 16.02 a rise of 5.62%.
So, instead of falling or remaining steady, my PSA has actually gone up
My alkaline phosphatase levels are at 87 (range 40-150) which is good. Kidney and liver tests are normal and so are my Vitamin D levels.
Will take another round of blood tests on the 22nd of May.
Any comments, anyone ?? I know I have to wait...give it time....etc, etc, etc. Any insights into WHY my bloody PSA just keeps going up ?? My next PSMA PET-CT scan is scheduled for end, July 2019 earliest after taking the second infusion.
Thank you very much for any insights.
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whatsinaname
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Hi Carlos....I think its been said more than once that an explosive rise in PSA after radiologic treatment is not unexpected...so your results are somewhat ambiguous....but the 'one man one cancer' caveat..as I like to call our condition, always applies. Take comfort in the great implied liver and kidney function enzyme results. Can you suggest your 'quacks' test chromogranin A levels to better understand any NEPC resolution....seems logical.
Yes, I have done the chromogranin A test and it was negative for NEPC. Since my quacks were not willing to recommend that I do the test, I just got it done anyways In Bombay, we are fortunate in that respect. Thanks, Jeff !!!
Since, I tested negative for NEPC, I did not ask any of the doctors I am in touch with. I tried doing a search of this forum but "Hidden" who has done Lu-177 also was not able to say categorically whether Lu-177 helped patients with NEPC.
As expected ALL my doctors ( I spoke to 3 of them) told me a flare up in PSA is nothing to be worried about and that the PSA test taken after 6 weeks to 8 weeks will indicate the true picture. The next infusion is scheduled for the 25th of June.
Absolutely, cesanon. At least that is what everyone seems to be saying.
Thanks again and all the very best to you.
I wouldn't read too much into that PSA change, especially if ALK Phos is still well within range. My doctor always tells me that we are treating the cancer, not the PSA. Once you see what's going on with the imaging, you can get a better idea what's happening with the cancer. Hoping for the best with your treatments.
Most therapies that kill prostate cancer cells will increase PSA temporarily. PSA is a protein on every prostate cancer cells, so when they die, it gets released into the serum.
There is also a stimulated regrowth effect (called "repopulation") from radiation. The radiation kills the outermost layers of each tumor first. This gives the inner parts of the tumor room to grow and access to blood supply. With multiple treatments, the entire tumor is wiped out.
You should not expect a decrease of the PSA until 6 weeks after the treatment. When I had the treatment in Germany they asked me to wait 6 weeks to measure the PSA.
Just thought i'd say hi and try to give you some encouragement by wishing you all the best in your treatments going forward. You are having a shitty time with the disease even though you seem to be doing "all the right things". Lets hope you are one of the lucky people able to post in the future your PSA is down below one and all your mets have cleared up and gone away!
No advice, just well wishes for you. You've been doing everything you can with a good attitude. You definitely deserve some good luck, a huge drop in PSA, and a clean scan.
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