Experiences with

Nuprin

Hi all,I had RT about 2 years ago and have been having 3 monthly Lupron jabs. My PSA has been rising steadily from a low of 0.02 ug/l (May, 2024) to 0.04 ug/l (August, 2024) The result of my blood test today is 0.09 ug/l (Nov, 2024). My PSA seems to be doubling every 3 months. Is this cause

hello, I just had a pet scan after my PSA went from .3 to 5.68 in 3 months time and it revealed 3 spots that my onc feels we should radiate. I am 3 years into this and have had 6 rounds of chemo and am currently on daro+ lupron. It took 6 weeks to get the scan and results and now my consult is in

hello everyone. I am new here but I’ve been watching your thread for a little while now. My father was diagnosed with advanced prostate cancer almost 30 years ago. He was 47 at the time. He had a PSA of 104 and a Gleeson of 4+2 at time of diagnosis. His cancer was always androgen dependent and he did

I read this and the advanced prostrate cancer thread everyday so I thought I would post my 15 month update to my radiation cancer treatment. It may encourage some of you. I was diagnosed with unfavorable intermediate risk cancer of 4+3 with three spots of PI-RAD category 5. Upon biopsy I had cancer

On Abby and Lupron for two years. For years before APC, WBC measurements were fairly low at 4K/microliter. Normal monthly trends were averaging around 3.5 to 4 with a spike toward nirvana during hospital stays. Yesterday’s measurements were an extremely discouraging 2.5k per microliter. So the plan

Here is a general toxicity ranking for the drugs you listed, considering overall toxicity across systems, including liver, kidney, cardiovascular, and other potential toxicities. The ranking is organized from most toxic to least toxic, with explanations. --- Toxicity Ranking for Overall Toxicity 1. Cabazitaxel

Have not been on here for awhile so I'll update. Had 15 weeks of prostate radiation from in June to August. Was not as bad as I feared. Seems my PSA has gone from 14 to 0.05 since ending the last dose of radiation. I'm told I have to stay on lupron injection and Nubeqa for the next 2 years as a precaution

looking for a good oncologist to treat my dads prostate cancer. Looking for a kind, good doctor who looks into the whole person. His current oncologist doesn’t pay attention to his complaints- like suddenly not being able to walk, and has said that if he doesn’t respond to lupron, oh, well. I am a

2014 brachytherapy, 2018 salvage prostatectomy, lupron, abitaterone/ presnidone, xofigo, docetaxel, pluvicto, PSA rose to 70. Roller coaster ride after 2018 with each treatment except pluvicto, psa rose from 20 to 40 now 70.

I was on Lupron and Abiraterone + Pred for 2 years. I completed both in early June, so I am now 5+months post-ADT. My T is only now starting to return (was 32 last week). However, my cortisol levels are still very low. I suspect this is the cause of sore joints that I have experienced since ending

Any body doing hormone medicine. i am doing lupron shot every three months. i am also taking prednisone and abiratrone. well i had to stop the prednisone and abiratrone due to high liver enzymes but doc wants to resume at half dosage..soon..saying all of that, wife questions whether i need to be on

Has anyone had experience with muscle pain while doing BAT therapy? I have 4th stage prostate cancer and I have been doing Nubeqa and Orgovyx this year. My PSA has been slowly rising, going from a low of 3.9 in July to 7.3 in October. I am trying to resensitize the cancer cells to the ADT using BAT

Husband's medical oncologist left MSK without assigning a replacement. We live in TN, and he would travel twice a year for his Lupron shot and Zytiga prescription renewals. This might be a good time to find a good doctor closer. Any recommendations for a doctor near Nashville?

my biggest fear since this began has been reading side effects from ADT (especially being relatively young, having a very attractive wife and excellent, mutually-satisfying sex lives. I’m over 3 weeks into Lupron (3 month). Zero side effects. Not complaining, but wondering if this is fairly common

I recently had my second Lupron injection, also on Xtandi. I’ve noticed over the past few weeks that my taste buds are off. Anyone experienced something similar?

I'm on Lupron and Zytiga/Prednisone. So far very successful in dropping PSA levels to undetectable. With this comes the usual side effect of everything being quiet 'down there'. Recently, I've had erections in the middle of the night. Just a couple over a period of a few weeks. Under normal circumstances

Metastisized per PSMA PET Scan/CT before SBRT treatment. Stopped taking Xtandi just after last SBRT treatment 4/30/2024, 3/12/2024 Lupron expired early Steptember. PSA readings: May=0.023, July 0.05, October 0.9.89Radiologist directed me to stop taking all hormone theropy on or after last treatment

Can anybody point me towards info that talks about how long it takes for PSA rise or testosterone levels to rise after missing my monthly injection?I should have had my Lupron injection two weeks back. For certain reasons I only have them monthly now whereas before it was every 3 months. How long have

Early yesterday morning, I got my 4th ADT injection (the every 6 month version). As the day progressed, I seemed more and more fatigued and eventually just went to bed after lunch. I also had just the slightest hint of a headache, and I never have headaches. I don’t recall any such after-effects

Im going to be on Medicare 01 Jan 2025. My Lupron shot is due 17 Jan 2025 Earliest appointment is 15 Jan 2025 at UCLA Will my new Onc be able to give me a Lupron shot on the 15th, or will I need Medicare preauth??