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Hi Phil,
My husband was first diagnosed in 2005 after a local biopsy, and testing seemed to show that the cancer had not spread outside the prostate capsule, so he was treated locally with only brachytherapy and external beam radiation to his pelvic area. All seemed well for six years, when a sharply rising PSA alerted us to a recurrence. That is when my husband referred himself to Mayo and Dr Kwon. We don't know if the cancer was already metastatic in 2005, or whether it became so sometime in the next six years. It was explained to us that the prostate cancer sort of seeds the bloodstream with cancer cells, which circulate around until they finally create a metastasis, but we don't know at what point that happened. The treatment protocol at Mayo has been jokingly described to us as "whack a mole," and what follows explains why. Between 2011 and 2016, my husband had several rounds and types of radiation at Mayo, and was on various medications during that time, including bicalutamide and others I can't recall now. In 2016 it became clear that the metastases were coming fast and furious, and that chasing them with spot radiation was no longer controlling them, and that is when docetaxel was prescribed. That kept the cancer quiet for some time, but eventually more rounds and types of radiation were necessary, along with abiraterone and prednisone starting in January 2020, which kept the cancer in remission for over three years until the next recurrence. Finally in January of 2024, my husband began Pluvicto treatments, which lasted until August of 2024. It was only moderately successful. Xtandi was begun in January 2025 but was discontinued after four weeks due to bad side effects, which my husband never had with Zytiga/abiraterone. More radiation at Mayo in March 2025, after which the PSA dropped some but did not became undetectable. Scans in June 2025 didn't show where the active cancer is hiding, so we return in September 2025 for scans and labs and a conversation about what to try next.

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Replies to "Hi Phil, My husband was first diagnosed in 2005 after a local biopsy, and testing seemed..."

You should ask about getting Nubeqa (Darolutamide). The side effects are minimal compared to Xtandi And it works quite well. After 15 years and four remissions, I’ve had 20 months in a row with An undetectable PSA. I had Zytiga for 2 1/2 years and was only undetectable for one month.

I know a lot of people that attend the Ancan.Org Weekly online advanced prostate cancer meetings that have switched to Nubeqa And it works quite well for them. Almost all of them have had advanced prostate cancer for a long time and many are only on Nubeqa because it keeps their PSA undetectable and testosterone isn’t a problem, it works around it.

Hopefully your husband’s cancer can be treated successfully.

My God, what a scourge for both of you…but he’s still chugging along so that’s what counts, right?
Compared to today, 2005 was the Dark Ages for PCa…who knew the significance of cribriform/IDC on biopsies? And now we have PSMA, Decipher and other genomic tests to help decide which treatment might be best. Today, your husband’s treatment might have been vastly different - and 20 years from now who knows??
Whack- Mole might become the gold standard for all we know, right?😆
Phil