For those who have undergone lu177 treatment of mcrpc, either through the vision trial or abroad, can you please share your PSA results, both during the treatment and also after the treatment was completed.
Thanks in advance.
For those who have undergone lu177 treatment of mcrpc, either through the vision trial or abroad, can you please share your PSA results, both during the treatment and also after the treatment was completed.
Thanks in advance.
Have you taken the treatment or are you thinking about it?
Did you make it back for a second treatment?
Yes, on March 17. My next treatment is next week on May 7.
My concern is my PSA which went from 85 to 55 after my first treatment (which was good.) My PSA has gone back up to 84 after my second treatment, which I’m hoping is due to more tumor kill and PSA release, but fear it might be something else.
I forgot, did you have an FDG PET too?
No FDG pet, but ALL my lesions on ct scan were intensely Psma avid.
Great! Hopefully any intra-tumor heterogeneity gets killed in the cross-fire.
If you see Haberkorn, ask him if he's started treating patients with Lu-177-FAPI.
Nobody gets to see Dr Haberkorn. Only get to see his protégés.
Do you think I need to be worried about the PSA increases since the last treatment, or too early to tell? I had a 45% decrease after my first treatment, so I was hoping for something similar, but not to be.
Tall_Allen
I looked up Lu-177-FAPI on your blog at:
pcnrv.blogspot.com/2019/12/...
It looks interesting. It appears to be the ligand.
One issue I have with PMSA Ligand is that that it is attracted to and/or processed by your kidneys and salivary glands. It can damage them.
Does FAPI have any such drawbacks?
Any other pros and cons for FAPI?
Is there anything that PMSA ligands are likely to do better than FAPI ligands?
I ave recently had my 5th Lu177 treatment and overall my PSA has gone from 1,584 down to 167 most recently (although I had a blood test yesterday and am awaiting the results). The biggest changes were after treatments 1 and 2 with the PSA roughly being halved each time, things have slowed a little bit now.
The other important factor with the treatment are the PET Scans, my most recent one after treatment 4 showed that all tumours had reduced in size by 50%.
There is talk about having additional treatments so maybe up to 8, with 7 and 8 being spaced further apart.
I suppose for me the worry is that as soon as treatment stops then the cancer will bounce back.
I am having treatment privately in London.
Hope this helps?
Best wishes for a fantastic outcome after the Lu 177. warm wishes
Today I heard from one of the doctors in Heidelberg. They are going to increase the amount of Ac and decrease the amount of Lu for my treatment next week.
I am unaware of that. I have not had significant dry mouth, only while sleeping. Eating has not been an issue.