I never had high PSA. My PC was discovered by accident (in 2014) when I was being treated for excessive nightly urination. A biopsy showed all areas of my prostate to contain high Gleason (9) PC. The biopsy also showed that the cancer cells were highly deformed and produced only low levels of PSA. ADT (degarilex) and radiation (brachytherapy and external beam) controlled everything for a while but in fall of 2016 the cancer spread through the lymph system to bones, lungs, and liver. I am now on chemotherapy (doxitaxil and carboplatin) along with ADT. Dr. believes that the immediate problem is controlling the progression in the liver which biopsy shows has the same characteristics as the cancer in the prostate. Next CT scan is next week (March 2016) after which i should know if the treatment is working. Dr. also says that these treatments should work until they don't work, which does not give me a good feeling. Apparently the cancer in the liver is also very dispersed so surgery or direct chemo would not work there.
I am particularly interested in what works to control low PSA cancer cells, and how to treat prostate cancer which has spread to the liver.
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Excellent video. I am a little confused about the idea of negative PSA, what does that mean? Does it mean that the cells produce less than the normal amount of PSA or does it mean that the cells actually absorbs PSA produced by other cells? I have been told that my cells are highly deformed and as a result produce very low levels of PSA. Are they negative PSA cells? When I started chemo using taxotere, I saw my PSA rise at first and then drop on subsequent treatments so that follows with Dr. Myers statement.
Dr. Myers also notes the role of stem cells and the need to kill or remove them from the body. The stem cells must be mixed in with the cancer cells. Can the stem cells be seen on conventional scans. he did not indicate that the stem cells can be killed with chemicals. he indicated stem cells needed radiation or surgery to eliminate them form the body, which is not that easy with metastatic spread of the cancer.
"PSA-negative" simply means cells that produce no PSA (not negative PSA).
My understanding is that stem cells are always PSA-negative. They do not require androgen & lack the androgen receptor - which is why therapy that targets androgen or the androgen receptor cannot kill them.
The concept of stem-like progenitor cells was by no means accepted when I was diagnosed. So it is not surprising that traditional therapies do not target them.
There are some natural otc substances that seem to selectively kill those cells. And Metformin:
For PSA-positive cells, the amount of PSA produced can be much lower or higher than average. PSA is not necessarily a marker of tumor burden. More significant is the PSA doubling-time [PSADT].
When undergoing a change of therapy, one should not panic if PSADT initially shortens. For instance, there might be an increase in PSA leakage from damaged cells. Ultimately though, the trend will become apparent.
when I got a biopsy ,I had only one out of 12 sample cores was positive.which is the lowest level that can be determine to have prostate cancer. I am on HTherapy right now. after reading about metformin made me wonder if it kept my pcancer biopsy from being at a higher rate of sample cores being positive. hopefully slowed it down too. I have actually depleted my intake of sugar for my diabetes and now I won't be eating fruit during my protocols to fight the pcancer. I read that sugar from fruit is almost as bad as refined sugar for prostate cancer. I am starting to think anything I eat will make my pcancer grow.
I pray every day I wake up and thank the lord for it.
I don't have diabetes, but I do take 2,000mg Metformin daily, in divided doses. This is the dose that Dr. Myers recommends.
Obviously, as a diabetic, you want to control glucose levels. Some people expect fruit to contain fructose, which is a safe sweetener for diabetics, I believe, but fruit contains a mix of sugars. Some fruits contain a certain amount of free glucose & should be avoided, but there are safe fruits.
Strawberries & blueberries are safe, & the phytochemicals might be beneficial against PCa.
Munching on nuts will slow down absorption of the sugars in fruit.
Apples are safe too, & the fiber slows down absorption.
But the best advice on the subject would be from a diabetic site.
pjoshea13 thank you for the reply, I have been eating a lot fruit and veggies, low consumption of meat. then I read about the sugar in fruit. I will check out some diabetic listings on google.
I take 500 mg twice a day. hoping it has been working to slow the progression of my Pcancer. it has been keeping my diabetic numbers at a normal range with my diet too.
My husband's PSA was never over 40, but he has Gleason 9, distant mets, and bad cancer cells. In other words, really aggressive cancer. The PSA is a relative number based on each individual. Some men go into the 1000s (understandably scary!) but some don't every break into triple digits.
Also have testosterone checked.
Once one has advanced PCa, it is a combination of PSA, scans, and other tests that really determines where you are.
Very true. Even after my cancer spread rapidly, my PSA never was over 25. It is going down now that I am on ADT and Chemotherapy. I am at 2.5 after 6 Chemo sessions.
I was diagnosed Gleason 8 with a very palpable tumor ... and a PSA of only 2.7. After watching the video, I am thinking that I need to find a cracker-jack oncologist who understands that low PSA cancer isn't something to be trifled with. So, eggraj8, I am as interested as you are. Good luck.
As Joel T says in the post above very aggressive PC produces low PSA. I am finding that many people have this type of cancer, but each oncologist only sees just a small percentage of patients with this type of cancer. So finding a cracker-jack oncologist who understands low PSA cancer is a challenge. Most oncologists seem to want to treat it like the more common high PSA PC.
My partner also had Gleeson 8 and a PSA of 16 at its worst!!! With a PSA of 11 generally for 18 months, they did nothing and didnt even check for prostate cancer... Had one met only in lymph node so robotic surgery, ADT, radio and now chemo to make sure the bugger is defeated. But high Gleeson dont always show up as high PSA.
My husband is on the same path as you are. His liver mets were diagnosed in January 2016 (he also had widespread bone mets) and he is currently taking carboplatin and etoposide with Lupron and Zometa. He is currently about to have his fourth cycle on chemo (three straight days) that occur every three weeks. When originally diagnosed, we were told he had approximately one year but I look at him and wonder how that can be as in spite of the chemo he seems outwardly to be healthy and managing the side effects pretty well. I look forward to following your posts and hope to learn more about your journey. I wish you the best as you continue your treatment.
I clicked on you and will follow you also on this blog as you are right, your husband and I are on the same path. When I first thought I had a year or less I was very depressed, but now I have learned to appreciate the time I have left whether it be a day, month, year or even twenty years. Hopefully, it will be the twenty years but who really knows. I understand that many new drugs are being tested and hopefully both your husband and I will be able to utilize them.
I recently walked one of my sons down the aisle and played with my grandchildren. I also hugged my wife and children. While life is not what we cancer patients originally hoped it is important for us to enjoy our lives one day at a time and appreciate what we have. Your husband has a wonderful wife and probably more to be appreciative of. Keep the spirits up.
Have you considered immunotherapy (sorry forgetting the drug name right now)? And possibly Xofigo -- a diffuse radiation treatment via IV that goes after scattered bone mets.
I asked about immunotherapy, but my DNA is not typical of the immunotherapies which are used for certain prostate cancers. My major problem is with the liver and to use a drug which goes after my bone mets will require stopping the chemo which hopefully is now controlling the cancer in the liver. I think the Radium 223 is very promising for bone mets but not for me now. It is hard to fight the cancer in multiple sites at the same time when many drugs are site specific.
Oh yes, sorry. Visceral (organ) involvement does foreclose the immunotherapy. Sorry. We think the RA 223 did do it's job. My husband made it through 4 of 6 treatments. He was just a bit sensitive to it but his bone scans have been good since, no new spots so maybe we actually did get some buggers early! Wishing you well sorting this out.
Something on small cell prostate cancer (which makes less/no PSA)
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