As I understand it, when PCa is treated with radiation therapy, the theory is cancer cells are more vulnerable to radiation because they divide more rapidly than normal cells, and they do not repair damage from radiation, while normal cells can.
The situation seems to be complicated if the person has BPH, since that would also contribute to the total PSA.
So the PSA comes from Normal prostate cells + BPH prostate cells, + PCa cells.
If someone started with a low volume PCa, that was treated with radiation therapy, verses someone with a large volume PCa that was treated with radiation therapy, wouldn't that imply the NADIR for the small volume PCa would be higher than the NADIR for a large volume PCa, since the low volume PCa also would have more normal cells, that would be less damaged than the radiation?
The reason I ask this question is because I see various places indicate that after radiation therapy the PSA should be less than a certain amount, but wouldn't that PSA value depend if it was a large volume PCa verses a small volume PCa?
It is easy to understand if the entire prostate is removed, because in that cause there should be zero PSA, unless something was left behind.
Any thoughts how they determine what the NADIR should be after radiation therapy?
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Nadir is specific to each individual. Simply put lower is better though getting there longer seems to be better than quicker. With radiation progression is considered either 3 rises is PSA in a row, as it may bounce, or nadir + 2.0. Not sure about low volume or high volume as I have never seen that quantified on anything during my treatment. I guess more mets might be higher volume, or a larger PG but neither of those correlated to a volume in my treatment. Hope I answered your question or at least part of it.
No they’re not. They said the PSMA does not indicate lymph node involvement. It is equivocal. Both the radiologist and radiation oncologist indicated they see a lot of this in practice, and it isn’t uncommon.
I am waiting on decipher results, and will be consulting with a Prostate oncology specialist, and at least one other person on this to see if they concur. Needless to say I am still concerned, even though there was NOT enough increase in radiotracer uptake to suggest cancer, which is why I will be consulting with a couple of other physicians.
I read your bio also treedown. Do you mind sharing where you went for treatment?
Your results look terrific, and I wish you much continued success.
Nadirs below 0.5 have an especially good prognosis. But it can take 3-5 years to reach nadir with bounces along the way. Prostatitis can cause disturbing bounces. BPH tends to go away because the prostate shrinks and hyperplastic cells undergo apoptosis.
So that implies if the radiation therapy if done correctly, most of the "normal" Prostate cells don't survive while hopefully all with all the Pca cells are eradicated.
Why I ask the question is because I plan to go through radiation treatment for intermediate 3+4 PCa, located in the left anterior, employing SBRT, and what I have come across is that depending on the radiation damage, normal prostate tissue has the ability to repair itself, while the PCa cells, by their very nature lack that ability.
Surprised that it can take as long as 5 years to reach nadir for some,
I think these are things that are good to know before having radiation therapy to psychologically prepare for that.
Most healthy cells survive, some are replaced by healthier cells. Healthy cells can self-repair, cancerous cells can't. Those healthy cells that can't self-repair self destruct (apoptosis) and are replaced. The cancerous cells (which cannot undergo apoptosis) that are not killed immediately will die later (even years later) in a process called mitotic catastrophe.
Yes, radiation therapy takes some patience. You're in it for the long haul.
Do I understand you correctly that after e.g. whole pelvic radiation, a patient’s tumor cells could experience not only (1) some immediate death from the ionizing radiation and (2) some short-term (on the order of months) delayed death upon attempting to replicate with damaged DNA (which is how I’ve understood thing so far) , but also (3) some longer-term delayed death (on the order of years) via mitotic catastrophe?
Wikipedia tells me that mitotic catastrophe can be induced by chemical stress. Could this include ADT + zytiga, for example?
2 & 3 are the same. Mitosis may be delayed by a cancer-protective mechanism, like dormancy, but will eventually happen.
An activated androgen receptor is necessary for cell replication. When it can't be activated, and the cell enters mitosis, the cancer cell dies. But some cells enter a protective state of dormancy or otherwise evolve to need less activation.
I had SBRT 2 years ago at age 81 and since then have had no SEs and my PSA ..which was 19.3 when i had treatment...has gone down from 4.99 to 1.27 6 months ago. Am having an updated PSA this week and hoping for further reduction. Back when i had treatment i refused any ADT so that is probably also an issue, but my RO at Emory is happy with my progress and i have never had any SEs other than needing to use Flomax for about 9 months. I feel fortunate after being on AS for 6 years. One thing that makes me curious is that my RO has added a Testosterone test to my PSA test order for some reason. My ED is pretty much permanent at my age so i dont know what the T test is for, but I plan to ask after the results come in. Have never had a T test that i know of. My RO says that it would take 3 increasing PSA tests before we would want to take additional action. With heart disease and T2 diabetes I suspect he may think i wont be around that long but i plan to be! I particularly appreciate the advice i have received from Tall_Allen over the years in making important decisions.
Yes, my nadir got to be 0.03 after ADT 6 months implants and had stayed there for 2 years then last month went to 0.04. I could not see the effects of radiation ☢️ on PSA as the nadir (0.03) was reached before RT. 🙉🙊🙊🙊🙊🙈
Here is what I can add from experience. The caveat is that TA, and Kwon of Mayo will both tell you don't confuse PSA with Cancer. There are many stories of PCa advancing with low PSA. I had SBRT (aka MSK Precise image guided) of the primary prostate gland 5 treatments over 8 days + 3 treatments of T5 in spine ending on Jan 20, 2022. Dr McBride at MSK strongly urged that NO PSA TEST FOR 3 Months. Stating we are killing many PCa cells and those give off PSA. Said RT will kill cells for 18 months, sometimes 24 months, but at 3 mos, we hope to see a drop in PSA. My prev low nadir was .260 Dec 2, 2021, after 15 months on ADT (Lupron/Abi-pred)=long slow drop. My first PSA after SBRT was earlier this month. A new low nadir of .095 =(-.165 since Dec 2nd). Made McBride, my Family, and Me happy, especially knowing that it should drop further for another 12-15 mos.
Look up Stampede Trial-Arm H. It proved in one of the largest Clinical Trials in the World that Men with low Metastaic Burden did much better with ADT + Radiation of the prostate gland. McBride said my 3 enlarged lymph nodes had shown significant shrinkage from 14mos of ADT, and said if that changes he could accurately ablate them with MSK Precise down the road. From a recent post this week on lymph node metastisis, I may move up that date before we see any enlargement of lymph nodes down the line. I agree with Treedown, and Magnus, above that each Man presents differently, and responds different from therapy. We are complex beings.
Hi Mike. Unless I read the criteria for that trial wrong, it selected patients with locally advanced or metastatic disease who are beginning ADT.
In my situation I asked the radiation oncologist if he would treat the pelvic lymph nodes, and he said no because the PSMA scan uptake was not enough to indicate cancer. I will be getting a couple more opinions on this in the next couple of weeks.
You are so right Spyder, nothing is straight forward.
Please see my post today of Phase 3 Trial posted in the Lancet of Pelvic Lymph Node Radiation. You must print and show your Radiation Oncologist. They are often so busy they get behind on their reading. Simple but true. Best, Mike
The issue in my situation is the PSMA could not determine if the pelvic lymph nodes had prostate cancer or not because there was not enough uptake of Pylarify to say it is.
I asked the radiation oncologist if he would treat the pelvic lymph area with radiation and ADT, and he said no, because the PSMA scan was equivocal, and they don't treat the lymphs unless it is definite. He also said it will be the decipher test that will determine whether to add ADT or not.
I will be consulting with Dr. Scholz and another radiation oncologist on this also, but I don't think they will treat an area unless it shows a definite reason to do so, and the PSMA does not indicate that in my case. The only other way I can see to determine that is if I had a radical prostatectomy where they could physically remove the lymph nodes and examine that, and I am not really inclined to do that.
There was none, and I suspect the reason for that is because the PSMA report indicated there was no increased radiotracer uptake. The report said they noticed a couple of "mildly prominent lymph nodes, 10x9mm and 17x8mm without increased radiotracer uptake from the PSMA.
They called it equivocal I suspect because it can be due to a lot of reasons. The MRI I had prior to the TP biopsy indicated no enlarged lymph nodes in the pelvis. I had the PSMA one month after the biopsy, and I wonder if the biopsy itself might have caused this, but I don't know.
The impression I have is they don't want to act on it unless the evidence shows it should be, so they just want to monitor it.
I am waiting on decipher results, and will be consulting with two other doctors to understand my options, and what course of action to take.
Thanks. Nothing is simple for any of us dealing with this
John when I was preparing for radiation my RO and I had a discussion about which type or length of treatment would be best for me.
After that she turned the discussion to the pelvic lymph nodes. Her rationale was pretty straight forward. Nothing was showing but we do not know what is hiding so she recommended that she radiate the pelvic area as well at the same time. I agreed.
It is my understanding that doing this is an area that some support and others do not. In my case I relied on her judgement since she knew much better than I.
Correct decision? Who really knows but one thing I learned in life and confirmed with this cancer is you make the best decisions based on the best data you have and you move forward and never look back.
As a old single seat driver I learned once I made the decision to pull the eject handles I would leave it up to the accident board to spend a year or so deciding if I made the correct decision in those few seconds I had based on the best data I had to make that decision. Same thing applies to this cancer.
Yes, there are risks w surgery or radiation. Did you ask if a biopsy of lymph nodes was possible? Possibly a needle biopsy?? I’m reaching for you to just ask the question?
No Spyder. I am not sure how easy it would be to access, in the pelvic area.
The point both by the urologist and radiation oncologist made is that in the PSMA scan report there was no increased PSMA uptake in the lymph which would definitely indicate a malignancy, just some mild swelling, and no different then uptake from normal tissue.
“Mildly prominent left common iliac node measuring 10 x 9 mm in CT image 264 without increased radiotracer uptake. It is nonspecific.
* Similarly, there is a nonspecific left obturator node on CT image 304 with mild PyL activity roughly equivalent to blood pool measuring 17 x 8 mm.”
They weren’t interested in acting on this at this time based on the report, and just want to monitor it.
I will be consulting with Mark Scholz in a week, and another radiation oncologist on their thoughts
I do appreciate your suggestions Spyder, and reading your profile, you have been through a lot, and have gained a lot of experience, and thank-you for sharing that experience.
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