New approved drug for pNETs
Good morning!
Yesterday I had a meeting with my oncologist to discuss the data from my last CT scan. I have been moved from scans every 3 mo the first year to every 4 mo the second and now am on 6 mo! Yay me :). Seems like Lanreotide/Somatouline is still working for me, scans showing stable disease, no new growth. Amd during the visit my very enthusiastic doctor shared a wonderfull news - FDA has approved a new ORAL drug for pNET patients who have previously been treated.
CABOMETYX® (cabozantinib) Patient Website https://share.google/k6P4TbdkKVD0O0u9Q
Thanks to science and some very smart chemists (colleagues
🙂 ) we have another tool in the toolbox!
Good luck to everyone on this journey!
Interested in more discussions like this? Go to the Neuroendocrine Tumors (NETs) Support Group.
Cabometyx (or cabozantinib) has been around since about 2010, recently approved for well-differentiated pNET and epNETs. Not sure that you would need it, as long as you are doing so well on lanreotide. There are many possible side-effects listed, in my case dizziness and dryness in the mouth along with a metallic taste.
I agree , but it is an option for when Lanreotide stops working!