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.
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Thanks for sharing your Pluvicto infusion story... I just finished my six infusions. I had a PSMA scan after the first four infusions, and it showed that the infusions had been beneficial in regards to my bone metastises... Question for you--- Did you have any bone scan (not bone density) after your fourth infusion?? If so, did you then have another scan after your sixth infusion to see what benefit there was (or not)??
Thanks again for your time/information... Mark
Yes, I had PET CTs prior to (2021), mid way through and after (6-22) my Pluvicto treatments. The treatments resulted in a remarkable reduction of lesions/tumors. Two years afterwards (6-24), things turned down, again and I am repeating the full 6 treatments under a very special arrangement. After the 3rd, treatment, 9 overall to-date, I had another PET CT to confirm the treatments are working, again. They are, and I will continue to receive the last 3 within the next 18 weeks.
I am 81 years old, coming to the end of the proverbial five year life cycle of stage IV prostate cancer which has metastasized throughout my bones and lymph nodes. I have had every treatment protocol available except chemotherapy which was my choice to not have.
I took the full Pluvicto course of six infusions, six weeks apart. I have to say I am the poster boy for Pluvicto. I tolerated it quite well. That is not to say that your results would be the same.
Every treatment has its better days and worse days. For me, the Pluvicto course was filled with way more better days than worse.
@preservationworks, welcome. Pain in your big toe is quite specific. metas2019 mentioned weakness in this discussion:
- Knee / thigh weakness after Pluvicto? Knee / thigh weakness after Pluvicto?
Are you noticing joint pain any where else?
Interesting about the gout like pain you described, @preservationworks. I've gone through chemo twice and Pluvicto. I'm currently repeating the full 6 Pluvicto treatments, now 9 total, 3 more to go. I had gout in my big toe a 40 years ago, so I know how that feels. I'm not a doc, but I'd have to say, I do not know of an association between Pluvicto and traditional gout systems. Please post any news you find. I'd be interested.
I am an active 86 year old and have prostate cancer. I complete chemo in April 2024. My PSA was 88 and came down to 9.5. Now it has gone back up to 44. I think Pluvicto is next. Can anyone tell me their experience with Pluvicto? I haven't decided my next step yet.
Some people have some major side effects from Pluvicto, most don’t. I have heard at least 5 people talk about their experience, In some cases they had to have more time between doses because of the side effects.
I saw a webinar where they discussed a person who lit up the Pet scan With metastasis from head to Legs. He had one Pluvicto Treatment and it almost cleared his pet scan, But his side effects were so bad that he could not take any more treatments
Be aware that it works really well for 33% of people OK for 33% of people and not at all for 33% of people.
If you have certain genetic issues, either hereditary or somatic, it can affect how well Pluvicto Works. You can ask for a somatic test before doing Pluvicto To find out if you’ve got Genetic changes Due to the cancer.
If you have BRCA2 or ATM It seems to work better. If you have RB1, PTEN or TP53 They are Pluvicto resistant. I don’t know if these are the only hereditary changes that cause Pluvicto To work much better or more poorly.
Thanks for the info.
This is the first I have heard about Genetic issues.
I start Pluvicto January 20th. Scheduled for six treatments 5-6 weeks apart. Should be interesting. I am classic 5 year aPC journey guy, terrible first year, followed by 2+ years of declining PSA (Hormone Therapy Responding) and now 1+ years slowly rising PSA. Next stop Pluvicto, after that we'll see.
Looks like we are in the same boat.
I started with hormone therapy in 2012, then seed implants in 2014 while continuing the lupron therapy. My PSA started rising the fall of 2023. I started chemo then and finished 9 treatments of the chemo April 2024.
I had a PET scam last week and I am scheduled to see
my doctor this coming week.