Anyone have experience w Apalutamide? After RALP, Lupron, RT & off Lupron 1.5y my PC has gone metastatic. Going back on Lupron & Apalutamde. Copay of $3K per month.
Familiarity with Apalutamide Effectiv... - Advanced Prostate...
Familiarity with Apalutamide Effectiveness, Costs?
Hi. I have been on apalutamide/Erleada for about 40 months. I am currently taking a 3 month break.
Check with Janssen, the drug’s manufacturer. They have programs in place for financial assistance. Go to Erleada.com best of luck
MJCA, looking at your Bio, if you don't mind, what were you on from 2005-2018. Thanks, for the link! What kind of SE's?
First Casodex and Lupron. Then I had seeds implanted. Then I believe 32 or 36 sessions of radiation. As my PSA went up, I would be placed on Lupron for 12-24 months. This happened about 4-5 times over the years. When my body rejected Lupron, that’s when I started Erleada.
Wow, quite the adventure, MJCA! Lupron was enough for me until I went off. T stayed in 200's & PSA <0.1. But when T jumped 35% to 330, PC went crazy. Hopefully, Lupron will do the trick & Erleada is a backup? I know we can take Erleada w or w/o food but do you have a preference of either or time of day? Thanks, so much for your input!
I have been on Erleada/Lupron for 23 months now, no issues that stop me working all day and PSA 0.02 with T 0.5. I'm so sorry to hear of a co-pay of $3000/month. Best of luck
I always worry about the fatigue issue, so I take it in the evening before bed, with or without food and I haven’t noticed any difference.
After my Radical Prostatectomy, my PSA jumped to 165 in just 4 months. Immediately went on Apaludamide ( Erleada ) and Lupron. Was down to .20 within 6 months. But I'm now climbing again and my PSA is 19.9 just the other day. Testosterone is 19 and the last scans look stable, so I don't know what the hell is going on with the PSA. I also started a Xofigo 6 month program two months ago as well as staying on the Erleada and Lupron. So three fatigue drugs now, I'm so used to it I don't really know the difference now.
The only two side effects that I noticed was the fatigue and hot flashes. I don't get the flashes much anymore, they come and go.
Sorry, to hear about your struggles. I am only 2 days into Erleada but some guys recommend taking it late at night, so fatigue coincides with sleep, I guess? I was on Lupron for 2.5 yrs., ending 1-1/2 years ago & only had "warm flashes" I would characterize them as. Made sure to exercise, run/jog, lift weights & may have helped. My wife is a retired Dietitian, so my diet is excellent, also. I will get monthly injections of Denosumab for bone health, also. Thanks for your input & try to stay the course, as best you can!
I’ve been taking Erleada for 24 months. No problems other than elevated liver enzymes shortly after starting. They resolved after lowering the dose for a few weeks and I’ve been taking the full dose since. I take all 4 pills with lunch everyday.
I quickly reached the $7K catastrophic coverage with my insurance now am only paying about $720/month for Erleada. 🤪