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Walterfrederick New User
Joined: 07 Oct 2008 Posts: 1 Location: Florida
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Posted: Thu Oct 09, 2008 11:52 am Post subject: Stage 4 PC |
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| This is my first post to this very informative forum.I was diagnosed with Pc in 2001.After much thought,my doctors and I decided that radioactive seeding was the best choice of treatment.That was traumatic but fine until 2005.My PSA was rising again.We then agreed on hormonal therapy.That worked until late 2007.My PSA was rising again.In March,with a PSA of 300+ we decided to start chemo after scans showed that the PC had metastisized.I started chemo with Taxotere and Prednisone.A shot of Neulasta 1-3 days after the chemo to help with my blood count so as to better stave off infection.My PSA soared in early Aug.to 3000+.Now,with consultations between my oncologist here in Florida and my wunderkind oncologist at Dana Farber it was decided that Carboplatin should be added to my treatment.It is given every 3 weeks by IV.when I get the taxotere.My PSA has come down to 1600 now.I will be having my 9th session of chemo.on Oct.14th and another PSA test will be taken and some scans are scheduled for the next week to see if there has been any metastisis progression.I'm feeling better since the carboplatin has been oredered.Still tire very easily but I get out every day at least for a short walk and lunch.I've lost 25 pounds.Megastrol has helped me maintain my appetite after a period of absolutely no appetite at all.I was slightly overweight at 210 before chemo started so I don't look overly thin.90% of my hair has been maintained.Is there anyone out there that is in a somewhat similar stage?I feel that I have very good care but this seems never ending.From what I read,my lifespan can't be measured in years but,over all I don't feel too bad.No pains which is a big plus. |
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Replicant Moderator

Joined: 01 Nov 2006 Posts: 220
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Posted: Thu Oct 09, 2008 1:32 pm Post subject: hi |
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I'm sorry to hear about the hand of cards you've been dealt. It's good to hear that the new med seems to be helping.
I'm guessing that the number of guys in this discussion forum that have hormone refractory prostate cancer is relatively low. I could be wrong on that point. But if you don't get sufficient replies, I would try out the Prostate Cancer Infolink Social Network, http://prostatecancerinfolink.ning.com/ , where there are guys in your shoes. The site is watched over by informed laypeople and medical professionals.
I wish you the best. _________________ Replicant
Dx Feb 2006, PSA 9 @age 43
RRP Apr 2006 - Gleason 3+4, T3a, N0M0, pos margins
PSA 5/06 <0.1, 8/06 0.2, 12/06 0.6, 1/07 0.7.
Salvage radiation (IMRT) total dose 70.2 Gy, Jan-Mar 2007@ age 44
PSA 6/07 0.1, 9/07 <0.1, 12/07 <0.1, 4/08 <0.1
http://pcabefore50.blogspot.com |
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camedia New User
Joined: 18 Sep 2008 Posts: 3 Location: California
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Posted: Thu Oct 09, 2008 1:45 pm Post subject: Similar to my dad |
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My dad was also diagnosed in 2001. He had radiation therapy first, and then he was given Lupron Depot shots starting around 2004/2005. Earlier this year after his PSA went above 150, his urologist prescribed Flutamide and later Casodex until his PSA rose to 355, and then he was referred to an oncologist for chemotherapy. He will get his third Taxotere injection next week.
My dad started having bone ache and mild fever earlier this year, before taking Flutamide and Casodex. After stopping Casodex recently, his pain went away, but nausea remains because of chemo. Zofran seems to help preventing nausea, but Megastrol is not improving his appetite. He started losing hair after the first chemo. |
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