Lupron Treatment Duration: How long were you on it?
I have been diagnosed with Grade 3 prostate cancer with a 4 + 3 Gleason score of 7. This after having 2 PSA scores last year between 4 and 7. The cancer has not spread to the bones. I have received two Lupron injections 3 months apart and will complete 28 radiation treatments in the next couple of days. No surgery. I have tolerated the Lupron shots well with few but manageable side effects. I have an appointment to receive a third Lupron shot next month. My first PSA test after completing radiation won't be scheduled for 3 months. From researching Lupron, it appears that this is used for advanced stages of prostate cancer. From what I was led to believe, I was not advanced. My question: How long and how many Lupron shots might I need to go through? I will have this discussion with my urologist hopefully before proceeding with the next shot. Thanks for any information provided by the group.
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A good friend was treated for prostate cancer 8 years. He had the Cyberknife radiation protocol and said it was so easy with respect to comfort or side effects that it was a non-event. His first every-six-months Lupron injection, on the other hand, left him unable to walk for a few weeks. He was not fully informed of the adverse effects and it took almost a year to fully recover full strength. Needless to say, he refused any further injections. In his case, the Lupron was thought to improve his cancer-free odds by 2%. Since his odds were estimated (for what it's worth) as under 5%, he thought the Lupron side effects weren't worth it. But everyone has a different experience and that was just his.
His PSA has remained low since the radiation and he takes no medicines.
Feel free to contact me as further questions arise, which they probably will.
My side effects were minimal (loose stools; slow urination), but they resolved themselves in 2 - 3 weeks. Careful targeting of the radiation, and separation of the colon from resting against the prostate, were likely the key there.
Now I just have to deal with taking Lupron (fatigue, some lethargy, weakness (noticed largely in the legs), and weight gain around the waist). One risk I'm concerned with is osteoporosis (bone fragility).
Dr. J
Thank you for taking the time to answer my post in detail. I have read it more than once and consider it my introduction into this new phase of our lives. The last sentence "“Note “ was very encouraging.
I'm 8 mos post surgery, started at psa 13.5 gleason 4+3. PSA started back up around 6 mos after surgery from .039-.091, had a clear PSMA PET CT and started radiation.
I'm on orgovyx instead of Lupron, but, in a recent conversation with my urologist he answered the how long questions with anywhere from 6 mos to 2 years max. It seemed the decision had more to do with my QOL and tolerance for the drug than anything else.
The radiation oncologist also told me that the decision was entirely mine and statistically, the percentage of better outcomes in my situation are only 3%-5%. My feeling is "give me everything ya got doc" at this point.
I was told it is usually 18 months , but some go as far as 24.
Definitely different depending on individual case so discussing with your docs is key. Good luck to you.
There's a long time adage about PCa: "If you can cut it out [prostate/PCa] and put it in a jar, you've cured it". That 's long been my mantra and my anticipated choice while working in the prostate Ca field. And that seems obvious if you are highly certain your PCa is confined to the prostate. Yet, when my surprise turn came at 79 yrs, with 30 years of monitoring PSA, a rising PSA over 4 yrs to 7 ng, led to a Gleason of 4+5, but a clear PSMA PET scan forced me to review this long held idea of the choice I would make. My final decision was based on three things; Fewer side effects with radiation (although ADT is not benign due to side effects), greater confidence in ruling out metastases (PSMA PET), and significant improvements in targeting the radiation (5 days at higher dosage) and minimizing the likelihood of side effects (e.g. Hydrogel placement, etc). So, a comparison of side effects flipped my prior assumptions of my treatment choice. Note: Advances have be sufficiently rapid that I found it difficult to make decisions based on published data in the literature because my judgement was they often do not reflect these current improvements.
Good luck to you both.
My husband was recently diagnosed with prostrate cancer . I am trying to learn as much as I can joined this group and your post jumped at me. It described our similar situation and the dilemma we are going through His PCP immediately said surgery but my husband is going back and forth between surgery vs radiation. PSA was 12 and the Gleason 3+4. Positive effects of a course of action is good to know but I want to know the negatives of either procedure. - surgery /radiation. Your post brought reality to the picture considering his age (76) and quality of life. I need to be prepared for whatever route he chooses. Thank you again
kujhawk1978 let me add a bit more to your excellent response.
First of all - as of this date Prostate Cancer is NOT curable. The cause is as of yet unknown. With no known cause there is no cure.
So with all the variables involved there is no simple single answer to the question of how much Lupron or when. All Lupron does is buy us time, it's no more than an insurance policy. Do you buy into it or not?? Lupron is your current insurance policy against recurrent cancer. It's your life and only your decision to make. It's not all that complicated. Do you want insurance or do you not want insurance. Once again, there is no current known cure for this cancer. You're the buyer so you decide.
We’ll said!
I had 43 radiation treatments and took Lupron for 25 months. At about 18 months I wanted to quit Lupron but my urologist would not let me. I regret his decision because I have been off Lupron for 3 years and have never regained my testosterone, which is now about 15, and I am deplete of energy all the time. I took a testosterone replacement for 5 weeks but my breast started to develop and I terminated the testosterone replacement. I'm afraid I'm stuck this way for life.