Can anyone share their experience with Pluvicto?
My 85 year old dad has prostate cancer that has metastasized to his bones. Zytiga is no longer effective. He is considering Pluvicto. I would appreciate input from those who have used Pluvicto.
Interested in more discussions like this? Go to the Prostate Cancer Support Group.
I received the first 6 Pluvicto infusions from Aug 2023 to April 2024 with very good results until Dec 2024 PSMA PET scans showed slight progression. I'm also approved for an additional 6 doses and got #7 last week. Same effects as always, slight flu like feeling fo 3 days but good now.
I'm younger (64) and have been fighting this already for 11 years , diagnosed in 2014 already inoperable stage 4 metastatic to pelvic region. I belong to several Pluvicto support groups and from what I've read on those, IMHO...non medical opinion, Pluvicto is good for people in reasonably good overall health. More elderly and frail people taking Pluvicto seem to have had bad outcomes, having to stop early and going downhill fast afterward, or dying during treatment. I think some good base overall health guidelines need to be established to screen prospective patients, not just blood work. Body condition and mass etc. need to be considered. They are starting Pluvicto earlier on, before chemo in some cases which may be a good idea as someone might not be dangerously "run down" from other treatments. ALWAYS discuss this with your doctor. I am not medically trained and my comments are purely from personal observations and reading. Best wishes to all.
@sillyoyster, were you able to ask your cancer team about these important questions about radiation exposure? Can the butterfly needle be used for you for Pluvicto infusions or how are they making delivery easier for your viens?
not yet. That's why I posted the question?
Did you have to take hormone stuff before starting this?
smc24,
I completed my 6th Pluvicto treatment Feb-24 and PSA was .2 until Dec 24 now PSA at 3.
Have contacted my MO for re-treatment of Pluvicto, but not covered by insurance; can you advise me best way to get another 6 treatments.
Best to you
I was one of the original clinical trial patients for what is now, Pluvicto. The pharmaceutical company, Novartis paid for that first round of treatments. I'm 4 of 6 treatments into my "repeat", and Medicare and my supplemental insurer is covering the costs. As you stated and as I learned, Pluvicto is only approved for one set of 6 treatments. So, to answer rayde0's question, I do not know and have not heard of a way to have the repeat round of treatments paid without being a clinical trial patient first.
I hope my experiences and outcome, so far extremely positive, will be a driver for the USFDA's approval of a second round of Pluvicto. But for now, I cannot help you. I know it's easy to say, but stay positive.
Thanks for your reply, will keep searching.
My husband, age 82, had his first Pluvicto treatment last Monday. He had some mild nausea, but he continues to suffer constant fatigue and leg weakness. At this point he can't walk any distance without having to sit down and rest. I would appreciate others' experience regarding the length of time this fatigue and extreme weakness may continue. Thank you, Kathy
I'm scheduled to begin Pluvicto next week. I've been on ADT for a couple years, cancer has now spread to bones and PSA is up a bit.
Question is: anyone out there receiving Pluvicto ALSO being treated for Pulmonary Fibrosis? I'm taking Ofev for the PF and curious about any interactions or reactions.
thanks
Scheduled April On Abiraterone now Did Xtandi, Radium 223 and 2 chemo's that caused my lungs to flood with fluid On oxygen for 6 months and prednisone gradually reducing
Lungs 50% now clear