Hello my brothers and sisters. After 3 years of ADT (Zoladex) and with a stable PSA of .13, my MO put me on vacation (to my great joy) I June, 2022. It has now been 5 months. Three months into my vacatión I could begin to feel the changes with greater strength, muscle mass and hope, although the hot flashes have continúed. During that period my PSA has been:. 136 - July
. 15 - Aug
. 132 - Sept.
. 189 - Oct.
.367 - Nov.
With the leaps in Oct. and doubling in Nov., I am begining to worry and would love the advice of the amazing people on this site. Am I in trouble? Do I need to think about going back on ADT? Is it time to try Estradiol patch es or Estro gel?
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CountryJoe
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Thanks for getting back so quickly TA. You have asked the key question. The MO had said a PSA of 6, since I still have my prostate. I had hoped for at least a year of vacatión before returning to ADT to knock PSA back down to . 13, and continúe with this plan for several years. I have no veins, so I don't want chemo.
Recently I finished my vacation when the PSA went from.6 to 2.6 after 6 months on my MO advice. I still have a prostrate & obviously the cancer as well.
I have locally advanced prostate cancer finished treatment 2016 I am on intermittent ht 6 monthly checkups psa 0.05 but my testosterone has not recovered and now I have been diagnosed with osteoporosis with low body weight, now waiting for treatment.
I have been back on firmagon ADT for three months now & have blood test next week so will update when I know the new PSA level. The monthly jabs in the stomach are becoming unbearable so will try Zoladex next.
Please keep us updated. I was on Zoladex before my vacatión and the SE were very tolerable. I just wanted my strength again. Best of luck to you my brother.
Have you had a PSMA PET to look for MET? At your PSA levels you are pushing 60% plus Sensitivity...wondering. Otherwise if it were me and the numbers are going up that means the PCa is growing...somewhere...the question is where? TNX
It should be as effective as any of the LHRH ADT drugs without the side effects. My T 'usually' doesn't go down to castrate levels; however, my PSAs have been undetectable for almost 4 years now.
I went on my vacation last month. After 2 years of Lupron, My PSA has been 0.03 and T=3, I still have my prostate. My oncologist said my target PSA is 3.5 as my PSA at the start of Lupron was 7.1. I’m scheduled to have blood tested every 90 days.
Maybe try some BROQ (sulforaphane) per this study for a couple months? This involved after RALP PSA progression so not sure if applies to those still with prostate.
I would not worry at all, sounds like you’re still on the good side of the fence. I remember asking the same question when I went on a Zytiga and later on a lupron vacation. I’m now CR, psa at 7 (wth prostate) I’m asymptomatic, T is still castrate only using estradiol and 1000mg Zytiga.
Thanks so much for this postive message, No_stone_unturned, I needed that. I live in El Salvador, and am in the public health system. Not too many options for treatment, just what ever the onc says. Will soon travel to the US for Xmas. Seeking a way to get access to estradiol paches or estrogel, following the bold path of Ron Ron. I wish you the best my brother.
I took a four year vacation but would not recommend it. My PSA reached 35. Since then I have taken Lupron continuously every three months and PSA is at <0.1. Your doubling time is worrisomely fast.
Thank you necessarilySo. The doubling time is what worried me. Im going to do another test before the end of December to see if this is a pattern. That's amazing that you took a 4 year vacatión and currently have a PSA of. 1. Why do you say you would not recomendó this????
The vacation was okay, but during the period, cancer cells spread to a few spots and I was fortunate to stop the vacation in time to reverse the problem. The Lupron with Xtandi brought my PSA down fairly quickly and the sore lymph nodes lost soreness in a couple of months. Others might not be so lucky.
I went on a vacation from Eligard and 12 months later my Testosterone began to rise but unfortunately, so did my PSA. My Oncologist prescribed Bicalutamide and this is keeping my PSA low while allowing my T to climb. We have now added Tamoxifen to counter my rising Estrogen. This strategy is working for me and I feel pretty good. Perhaps this could be an option for you. Keep strong, DD 😎
I have been off ADT for over a year and expect my next test to hit over 2.0 which will signify a BCR after initial treatment. At that point I will get scans and most likely go back on ADT. I was on Lupron taken alternately in left or right ass cheek every 3 months. Other than a little discomfort that day and night no other issues from the shots.I guess I don't understand how vacations will work going forward. TA says it's up to us but that doesn't clarify it for me. I hope at this point I have the chance to figure it all out.
Thanks Treedown (great name 😊). There are a number of respected "oldtimers" on this site who consider vacations dangerous. I'm an adventurer and need to know how agressive my cáncer is and how it will react to curtailing ADT. I just need to know that, although I am aware that this path might kill me 😊. In 5 months of vacatión, my PSA has gone from .13 to . 36. I would also love to be at 2 after a year.
My doubling time was 1.3 months so I am hoping that stays the same or slows down as opposed to the third option. I am also hoping to get an idea of how aggressive mine is as well. I have been on the forum long enough that even within the status of aggressive there's different levels.
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