Jevtana+carboplatin is a good next step. However, Lu-177-PSMA-617 is even better. While we wait for FDA approval of Lu-177-PSMA-617, there are several trials of it in the US:
No recent tissue has been biopsied yet. His PSMA numbers on the scan came very high - SUV max 20. Doc says its almost impossible for neuroendocrine to put out that much PSMA. So they're pretty confident its still Adenocarcinoma and are not looking for anything else.
I agree - I didn't mention neuroendocrine. I was wondering more about "double negative" if his AR expression is low, and possible indications for immunotherapy and PARP inhibitors.
Not working any more for me either.. Just 2 bony mets lit up on CT and NaF18 so starting radiation treatment tomorrow, Actually only set up and tattoos tomorrow, then High intensity radiation to my 2 mets.. Hope to get along a little longer this way. Jevtana/cabazitaxel would be a good choice as long as you don't have neuropathy from earlier treatments...
Not sure where you live, but LU-177 is offered outside the US if you can afford it and are able to travel to wherever it is offered.
If you're considering LU-177, it's recommended that he get an FDG scan as well as a PSMA scan (sounds like he already had that). It's been proven that patients with low PSMA expression or discordant FDG-avid disease don't get a good response from LU-177.
Of course as mentioned, there is also Jevtana. Has he had a biopsy to look at IHC and for genetic sequencing? That might help to determine if adding a platinum chemo could be helpful and also see if he has any treatable mutations such as ATM,
No recent biopsy done. Hence we are missing info on any possible mutations. Although our doc said that the probability of having any of these mutations where treatments are available is very low? I still agree that its required to know incase dad has any of these.
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