Any one with Neuroendocrine tumors getting the shot once a month?
I have heard there is side effects to the once a month shot( unsure of the name) what has any one experienced?
Interested in more discussions like this? Go to the Neuroendocrine Tumors (NETs) Support Group.
I appreciate you sharing your experience with lantreotid shots, @dbmenger. You said that you have "...no discernible tumors anywhere." As I don't recall your NETs history, I'm wondering if the tumors were removed surgically.
Hello @splendrous,
I look forward to hearing from you after you see your medical team this month. I hope that you get some helpful information on how to proceed. Will you post an update?
I am having the once per month injection of Octreotide (sp?). The drug has calmed my hot flashes and diarrhea. It also has kept the mets to my liver in check and not growing. I think this is working for me. This drug gave me no side affects which is onderful.
Good luck with your NET treatment.
Michelle
Hello @perryleeoneal and welcome to Connect. I appreciate you sharing your journey with NETs. From your post, it looks like you were diagnosed about 5 years ago. A lot of people, like me, had no symptoms, but the NETs were found incidentally. Was this true for you?
I look forward to hearing from you again and knowing how you are feeling since your surgery and if you are having any problems with blood sugar.
I have an injection of 125ml Lanreotide every 4 weeks, to stablise my NET in my Pancreas. I discovered that it had been there since 2018 but missed by Radiologists, now in metasised in my liver, 3 tiny tumours. Professor could not operate as my aerobic levels too low due to failed hip Replacement and too high a risk op.
Did the Radiotherapy reduce the liver Mets?
I was informed by U.K. Professor that Lutathera is not approved by NICE in U.K.?
I do know it is a very expensive treatment. Could that be the reason?
Yes!!! My last PET scan (a few weeks ago) showed ‘no new spread or tumor growth’ and a couple of tumors on my liver actually shrank! One shrank so much that it was no longer detectable on the scan. We were very pleased with the results. My oncologist said that I am considered to be in partial remission. I’ll take that news and run with it:) My motto remains…one day at a time! Wishing you well…❤️
Congratulations to you. Hearing that news had to feel great?