Stage 4 prostate cancer treatment options
I have recurring prostate cancer and it has found its way to 5 different bones, including my left shoulder and two ribs on my right side. I started 6 month Lupron shots but have been told that because it is stage 4 I need additional treatment. My oncologist is recommending either Abiraterone (Zytiga) for 33 months or 6 treatments of Docetaxel chemo. She says that they look to have very equal success. With the Zytiga I will also have to take steroids, probably prednisone which I understand includes possible liver damage. Six chemo treatments seems like a better approach but I have heard Zytiiga talked about in a very positive manner. I understand it can be expensive and I do worry my prescription drug coverage could change its formulary and raise my cost significantly as well. I've already had that happen with a drug I take for Parkinsons.. Just looking for some general input regarding peoples actual experience either way.
Interested in more discussions like this? Go to the Prostate Cancer Support Group.
Thanks everyone for the information on here.
I am going for my diagnosis on November 18th after multiple scans and biopsy so I will be following this site.
Thanks, Mel, for your very positive message. I have just been diagnosed with Stage 4 following a bone scan. Still waiting for my first oncology appointment and, hopefully, the start of a treatment plan. Enjoy Sandals and the sun. ☀️
Get the true results that you are castrate Sensitive then Get on barticulutimide then Zolodex
Save enzalutamide only if you're castrate resitive
Ask about radiation They nuked 1 inch cancer out of my L2 lumbar using GPS then Zolodex
Get mri scan for facts
Thank you for your positive submissions relating to stage 4 prostate cancer. They give hope in real experiences and help in navigating the dizzying array of other treatments, drugs, etc….
My journey is just beginning in Seattle. Recently diagnose with Gleason “8” and stage 4 with iliac lymph gland involvement. Bone scan next week. Starting bicalutimide this eve, bone scan in a week, and the 4 month interval (hormone?) injections a few days following bone scan. This has happened sooo quickly after a 351 psa. I am hoping this looks like a good course of treatment. 30 years ago I was referred to Mayo Clinic for evaluation of amyloidosis of skin. I was very impressed with quality of care then. So when I was browsing the Mayo website and found this support group, I jumped right in👍. Head swimming with uncertainty, and sometimes worse. Thank you all!
Hi
Hello Michael in BC, you and I are beginning a very similar journey. I would love to share experiences with you in this post. By the way I am 69 and have always thought of myself as fit and active, until now.
Thanks for reaching out, Donald (Don?). I just turned 73 and like you have been pretty healthy. Never ha a broken bone or an operation or a serious illness. All in all, can’t complain even with this current challenge. Kind of “pay back” time. Our (Sherry is part of the team) first oncology appointment was just scheduled for November 29th. Feeling somewhat relieved to have it on the calendar and yet another level of anxiety over the new info/prognosis/treatment plan we might receive. I’m trying to maintain a somewhat normal routine but every pang, pain & twitch, however unrelated, gives me pause.
Thanks for the rapid reply Michael. I am truly looking forward to communicating as our journeys as well as others unfold! We have a brotherhood here. Don
Before 40 days of radiation my PSA was 1300
after ,02 on zolodex
4 years later intense rad of L2 took 1 inch out of spine PSA 1,2
Hope springs eternal
Thank you Melcanada, looking forward to hearing more from you and all walking this path. As time goes forward I will share more of my experiences as well! For now it is 8:00 on a frosty but beautiful day in Seattle😎👍 Don