We are booked for first session of lutetium 24th of this month with Technical uni Munich they had a date sooner than h/berg . The assistant prof Matthias eiber has dealt with us all along and has been excellent .however today he informed us Dad would have to come off Xtandi whilst receiving lutetium ? Matthias stated that interactions between the two regimes are still not known. They would not recommend combination, butcannot refrain a patient by doing so. Has anyone else taken both at the same time? Or are there any studies to show safety and effectiveness of both together? Thanks
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Jenbt
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"Matthias stated that interactions between the two regimes are still not known." Dr. Eiber is right, it is unknown. However, studies with mice have shown, that Xtandi increases the PSMA expression and therefore should support the Lu177 therapy. Other clinics recommend to use Xtandi with Lu177 for that reason. There have been no studies with humans, however.
They could not refrain me from doing so. I used Bicalutamide to increase the PSMA expression. This will not increase as much as Xtandi though. At Bad Berka they asked me to use Xtandi instead, but my health insurance will not pay for that.
As far as I know there is not information indicating that Lu 177 PSMA treatment is associated with complications when the treated patients are taking enzalutamide or abiraterone. There is information indicating that abiraterone +prednisone and xofigo treatment (Radium 223) is associated with higher mortality and bone fractures. Perhaps Dr. Eibert is being cautious because of the problems encountered when Xofigo was administered in patients taking abiraterone.
Sometimes anti-androgens,like Xtandi, increase the PSMA avidity of tumors. Maybe that increase in PSMA makes lutetium less apt to kill the cell? Maybe not? Is that a gamble you are willing to take? If you are prudent, you would follow his directions.
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sonja is the person to contact in nuclear medicine i can't recall her second name but will get it for you when return if you email through the international department it will be directed to this lady who will set wheels in motion.
Tumor growth was delayed by ARB while 68Ga-PSMA11 uptake increased up to 2.3-fold over time when compared to controls. ABR-induced upregulation of PSMA expression was confirmed by flow cytometry. Phospho-γH2A.X levels increased 1.8- and 3.4-fold at 48 h in response to single treatment ENZ or RLT and ENZ+RLT, respectively. Despite significantly greater DNA damage and persistent increase of PSMA expression at the time of RLT, no additional tumor growth retardation was observed in the ENZ+RLT group (vs. RLT only, p = 0.372 at day 81). Median survival did not improve significantly when ENZ was combined with RLT.
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