Stage 4 Prostate Cancer and Hormone Therapy quit working
My husband is at Stage 4 for one and a half years now...The hormone therapy (Apalutamide and Erleada) seems to have quit working. For the past 8 months, his PSA keeps climbing. It's up to 12 now..
We're scared. Anyone else got to this point? How are you doing when the hormone therapy isn't working anymore.
Interested in more discussions like this? Go to the Prostate Cancer Support Group.
As an example of "If you're doing your own searching, the keywords you want are "metastatic castrate-resistant prostate cancer" (or "mCRPC") — those will give you the most-relevant results".- https://www.urotoday.com/conference-highlights/2024-south-central-section/155941-scs-aua-2024-clinical-trial-updates-for-treatment-of-metastatic-prostate-cancer.html?utm_source=newsletter_13520&utm_medium=email&utm_campaign=south-central-section-american-urological-association-aua-insights-in-prostate-cancer-treatment
Yes, but also a bit on the technical side. Unless you have a background in bioresearch, probably better to choose links that summarise the research for a general audience. You could try feeding the article into ChatGPT and asking for a summary, but be prepared for 1/4 to 1/3 of the things it says to be B.S. or otherwise completely wrong (that's my experience, anyway).
To proftom2
I have the same zillion spots. After 6 rounds of chemo and on Lupron, the second PET scan show my spots are the same. How long did it take for your spots to disappear?
Oldfords, First 3 CT scans revealed a zillion spots, that was the first 6 months of treatment. 2 Years after another CT scan the spots/clouds lessoned by half. Two months ago, my PSMA Pet Scan reveal 9 spots. Radiation Oncologist is going radiate 3 spots year in the next few weeks. I am now 3 years, 11 months on this journey. Hope this helps.
I’m very sorry to hear this. I’ve had much success with Enzalutimide and Firmagon mind you I believe my diet (Mediterranean) and the addition of naturopathic supplements are helping as well. Specifically, I take Pomi -T, Cucurmin, Quecetin, Super K and Vitamin D. My thinking is the supplements may boost the effectiveness of the Enzalutimide which apparently treats three types of PC whereas Apalutimide treats only two or so I was told. Just thought I would pass this along. Best wishes.
"Enzalutimide which apparently treats three types of PC whereas Apalutimide treats only two"
Thanks for sharing that. It's true, but it matters only if you have metastatic castrate-resistant prostate cancer (mCRPC), which is the one that Enzalutamide is approved for but Apalutamide is not.
Otherwise, if you have non-metastatic castrate-resistant prostate cancer (nmCRPC) or metastatic castrate-sensitive prostate cancer (mCSPC), you can take either (neither is approved for nmCSPC yet, as far as I know).
Hi there
I assumed the issuer of the post had mCRPC - yes/no? Just trying to help if this is the case. Also wanted to pass along diet and supplement routine for the same reason.
Best wishes
Not sure. Just adding to your post that supporting 2 vs 3 types wouldn't make a big difference, because either you can or can't take any a -lutamides for the particular cancer phase you're in (supporting other types brings you no benefit). Absolutely right that if the poster has mCRPC, then Apalutamide isn't approved yet for their situation.
Cheers!
Thanks It does give me hope that mine will begin to disappear also.
Darolutamide is the one to use. As the least side effects of all three, if you look at studies, we see that if fewer people drop Darolutamide than the other lutamides because of side effects. It has also been approved for mCSPS and mCRPC.
After 2.5 years on Zytiga I was undetectable for one month. With Darolutamide i’ve been undetectable for the last 11 months.