Are you a member of my club? After diagnosis and start of any treatment, have you had a PSA of over 180 continuously over the most recent 180 days, up to the present? I fear I'm in a class by myself.
Fortunately, I still don't have any metastases outside of bone and lymph, and chemo is making me feel better, even though my PSA is staying more or less constant, currently at 1500.
Written by
Beauxman
To view profiles and participate in discussions please or .
I pray for you every night. I'm happy you're feeling a little better with no more metastasis. But would feel a lot better seeing that PSA sliding down.
Here's one for you: Did you hear about the one armed fisherman who caught a fish this big? 🤚-------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------
Hey Beauxman I'm after your record. After 6 cycles of chemo I reached a PSA nadir of 1.8 in March this year. Following this I had 3 more cycles of docetaxal then 3 months of enzalutamide and I am now up to 6 weeks on PARP inhibitors. And with all that tratment I achieved a new personal high PSA of 200. Blood drawn yesterday. So I broke the 180 barrier only 1 day down so far but since nothing appears to make any dent in disease progression it may well stay there for the foreseeable future. 199 days to go and I can start the 200 club!
Wow, you started one year later than I, but your doubling time has been worse than mine, so your PSA is catching up. I'm sorry this is happening to you. I'm glad you got rid of your liver mets. I wonder if I have some liver mets that haven't been detected. I have never had a PSMA scan. I'll get my first one in January.
I am right there with you brother, actually I think I have you beat.
After my first chemo 6 rounds of Docetaxel in July-October 2016, PSA went from high at Dx of 658 to 1.46, lowest ever for me.
Then after a year of messing around with Casodex re-challenge, Zytiga, and then Xtandi, my PSA shot up from 2.25 in January 17 to 2250 in January 2018. Yikes!
So we started back on Docetaxel in January, and went 12 rounds. Liver mets showed up in September's CT and they switched me to Jevtana. The lowest my PSA has been this year after now 17 rounds of chemo is 840. So I have technically been over 800 for a full year.
It now ding-dongs between 975 and 850 - recent bloodowrk saw a drop of about 10%.
Good afternoon! I did a search for Dr. Antonarakis and found your post. That is who my Dad is seeing. We really like him a lot. Are you still under his care? My dad just started his first round of Docetaxal and has been very sick. He is on day five right now and his bone pain is bad and he feels very weak. He did not respond well to the hormone therapy and is now trying this. How are you doing with your treatment? Just looking for advice and support through this stressful process. Thanks!
Dr. Antonarakis is great, but my recent bone marrow transplant and bipolar androgen therapy were done through a clinical trial led by another John's Hopkins oncologist, Dr. Denmeade, so I'm communicating with Dr. Denmeade more often these days.
Did Docetaxel make your dad's bone pain worse for just a couple days? If so, try taking an antihistamine (Claratin) before the next infusion. That helped me a lot.
Content on HealthUnlocked does not replace the relationship between you and doctors or other healthcare professionals nor the advice you receive from them.
Never delay seeking advice or dialling emergency services because of something that you have read on HealthUnlocked.