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Hot flashes more than a year after ending treatment

Prostate Cancer | Last Active: Oct 30 5:26pm | Replies (28)

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Profile picture for Colleen Young, Connect Director @colleenyoung

@pesquallie, I noticed that you wished to post a URL to a Mayo Clinic News Network article with your post. You will be able to add URLs to your posts in a few days. There is a brief period where new members can't post links. We do this to deter spammers and keep the community safe. Allow me to post it for you.

Here is the link to the news story:
- Study Solves Testosterone’s Paradoxical Effects in Prostate Cancer https://corporate.dukehealth.org/news/study-solves-testosterones-paradoxical-effects-prostate-cancer

And to the actual study:
- Androgen receptor monomers and dimers regulate opposing biological processes in prostate cancer cells https://www.nature.com/articles/s41467-024-52032-y

I have to disagree with the statement about doctors not embracing advancing research. Research institutions like Duke, Mayo and others centers of excellence constantly pursue research to improve treatment approaches in efforts to develop more effective treatment and to reduce the burden of side effects for patients.

Understanding which patients benefit from which therapies and personalized medicine improves this experience. The Duke study sounds like a good discovery that hopefully will benefit patients (and providers). Please note that the study was conducted in the lab (in vitro) and not yet conducted in clinical studies with humans. That's when the rubber hits the road. 🙂

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Replies to "@pesquallie, I noticed that you wished to post a URL to a Mayo Clinic News Network..."

@colleenyoung

Thank you for the update. I tend to be pessimistic about my treatment because my family doctor discouraged me from having a PSA for 3 years during which time my PSA rose from a steady < 1.0 to 11.1. She did this because in 2014 the president's health committee recommended against PSA testing for men above 70. I was 82 when I finally got a test and then a biopsy with a Gleason 4+4. My bone scan was clear and my PET scan rating was stage T3b. I had 44 radiation treatments and 4 months of Lupron hormone. I had diarrhea and Tenesmus pain throughout my radiation treatment. After 4 months of Lupron treatment, I had serious painful side effects that included 24-hour sweats keeping me wet and restless at night, severe joint and muscle pain, headaches, pain at the injection sites, and urination every 2 hours. I had to stop the Lupron after 4 months because of the pain. Now 4 months after the end of Lupron treatment I am beginning to see a reduction in side effects. My urologist says that my side effects are abnormally bad and my recovery is slower than normal. I am hopeful but still very anxious.