Your husband is oligo metastatic and potentially curable. They have to radiate his Mets and prostate if it is possible. Contact a centre of excellence. For example Dana Farber cancer institute. You could at least ask Dana Farber Radiologist for second opinion.
Hey Seasid, thank you, I believe Dr Gordon Grado in Scottsdale would offer us some options, hope you are correct on curable,we were told by his MO it’s not, but that was at Dx, 4 years ago, lots of new treatments since just Chemo and Lupron, we all keep hoping and 🙏
That is correct. Now I have MRI Linac from Electa Unity locally where I live. It wasn't there 4 years ago. It is a high precision SBRT machine. Lots of changed since my diagnosis.
They should consider you on the case by case basis. I personally would still go to Dana Farber cancer institute if I could. They have a team. I personally believe that the most important is a team.
I should have a team, but I don't have it and that is very dangerous.
I should have an urologist, MO, RO and a neurologist and also a neurosurgeon in my team as a team, but I don't have it.
All this people competing with each other for job.
For example if you have an MO with a friend who is a urologist you will be most likely be referred to a urologist by your MO ones you will have difficulties to urinate. They will try to solve your problem with surgery.
The RO could kill your CRPC in your prostate with radiation so you don't have this problem, but your MO will not refer you to RO saying that Radiation will not extend your life according to STAMPEDE clinical trials.
I don't care (I am polimetastatic and not curable but still don't want to use catheter to urinate nor to develop total incontinence after surgery.
If you can go to the place where they have a team looking after you.
Treatment decisions are very important to extend your life. I can't advise you. I am not a doctor nor I am a centre of excellence like for example Dana Farber cancer institute is.
If I understood correctly, his PSA started to increase in 2022 after chemo and ADT.
The cancer is mCRPC. He is on Zytiga and ADT at the present time.
His PSA is stable around 0.4.
I believe that nothing should be done until there is evidence of radiographic progression of the cancer. It could be a good idea to get a PSMA PET/CT to follow the cancer evolution.
You could request Provenge a vaccine offering a survival advantage and discuss having a direct biopsy if there is evidence of new metastases.
He did have a PSMA scan in November , But it was so new at the time, I don’t think they were able to really interpret the results adequately enough which is why were seeing a second opinion RO here in AZ. Trying to see if radiation is recommended at this time
Hi, I've been getting an injection of elegard ever 3 months, and have been taking zytiga and prednisone for just over 2 years. I'm about to go on intermittent treatment. My PSA started out at 111 and is now .008, and my 3 metastases have shrunk to undetectable range. Keep it up. Hormone therapy works.
You may also want to incorporate ivermectin in your regiment as it does wonders in reducing psa as well as making the Pca sensitive again after it becomes crpc. It’s been used billions of times to treat other diseases and Is very safe n well tolerated… good luck
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