Welcome to the NETs Group! Come say hi.

Posted by Teresa, Volunteer Mentor @hopeful33250, Jan 20, 2017

Hello and welcome
Let's pull up our chairs in a circle and check in with each other and talk about how we are doing with our NET diagnosis. Any new tests, meds or treatments going on for you? What about your symptom control? Any concerns you have?

Interested in more discussions like this? Go to the Neuroendocrine Tumors (NETs) Support Group.

@kjstein

Yes, I was able to tolerate PRRT well. The treatments went exactly as they were explained and my major side effect was fatigue--really fatigued after the first treatment and less so with each of the remaining 3. For me the fatigue was most noticeable the first few days after treatment and lingered for about 2 weeks when I started to get some energy back! No nausea either during or after treatments--but I did notice that there were certain foods that I really craved and others that I just did not want to eat. I also did experience thinning hair (which I think may be unusual) but I did not lose all my hair! By the end of the 4th and final treatment, I did have mild anemia--but blood levels stayed within low end of normal limits throughout treatment. It is taking some time to build my strength back up, but I'm back to normal levels of exercise and feeling well now (about 4 months after last treatment). The protocols for after receiving the treatment are pretty strict (distance from other people and your pets for several days, laundry and bathroom protocols, etc.) but overall this treatment was not as scary as it sounds! Happy to share more if anyone else is thinking about this as a treatment. Just at the start of the journey, so will see how it goes from here!

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Hi again @kjstein

I appreciate you sharing your personal experience with PRRT as well as the good results. You might also find the Connect discussion group on PRRT interesting. Here is the link that will take you to that discussion, https://connect.mayoclinic.org/discussion/prrt-treatment/

As it would be good for prospective patients to have some first-hand knowledge, can I invite you to discussions with others who might be considering PRRT?

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@hopeful33250

Hi again @kjstein

I appreciate you sharing your personal experience with PRRT as well as the good results. You might also find the Connect discussion group on PRRT interesting. Here is the link that will take you to that discussion, https://connect.mayoclinic.org/discussion/prrt-treatment/

As it would be good for prospective patients to have some first-hand knowledge, can I invite you to discussions with others who might be considering PRRT?

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Yes that would be fine. I'm happy to share and thanks for connecting me to the PRRT discussion. These resources are wonderful.

Enjoyed meeting everyone yesterday at the virtual meeting and plan to be a future meetings...loved the sharing and positive attitudes of everyone on the group!

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@kjstein
It was great that you could attend! Yes, I will contact you when I see a member who wants some first hand information PRRT. Also, feel free to post to anyone you meet in any of the NET discussions. I'm sure you're input will be helpful.

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For all of you who are currently taking Octreotide for carcinoid syndrome, by injection, there is some good news for you. The FDA has recently approved an oral form of this medication.

Here is a link to the article, "Amryt Receives Orphan Drug Designation from the FDA for Mycapssa® (oral octreotide) for the Treatment of Carcinoid Syndrome"

https://www.globenewswire.com/news-release/2022/07/14/2479558/0/en/Amryt-Receives-Orphan-Drug-Designation-from-the-FDA-for-Mycapssa-oral-octreotide-for-the-Treatment-of-Carcinoid-Syndrome.html

Please note that Stage 3 trials of Mycapssa, to determine correct medication dosages, will begin sometime in 2023. We would not expect to see the drug become widely available until much later in 2023 and more likely early in 2024.

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@hopeful33250

For all of you who are currently taking Octreotide for carcinoid syndrome, by injection, there is some good news for you. The FDA has recently approved an oral form of this medication.

Here is a link to the article, "Amryt Receives Orphan Drug Designation from the FDA for Mycapssa® (oral octreotide) for the Treatment of Carcinoid Syndrome"

https://www.globenewswire.com/news-release/2022/07/14/2479558/0/en/Amryt-Receives-Orphan-Drug-Designation-from-the-FDA-for-Mycapssa-oral-octreotide-for-the-Treatment-of-Carcinoid-Syndrome.html

Please note that Stage 3 trials of Mycapssa, to determine correct medication dosages, will begin sometime in 2023. We would not expect to see the drug become widely available until much later in 2023 and more likely early in 2024.

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Great news
What is the difference between octreotide and lanreotide
I currently switched doctors and she gives octreotide I have had 3 doses of lanreotide
Please let me know
Thank you

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@sophiarose

Great news
What is the difference between octreotide and lanreotide
I currently switched doctors and she gives octreotide I have had 3 doses of lanreotide
Please let me know
Thank you

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Sorry I have been diagnosed with metastasized liver NETs don’t know where the primary is as of yet

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@sophiarose

Sorry I have been diagnosed with metastasized liver NETs don’t know where the primary is as of yet

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Hello @sophiarose

Personally, I have never taken either octreotide or lanreotide so I do not know the difference between the two. I understand that one is easier to inject than the other. Here is an article from the National Library of Medicine about the two different medications, https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6643159/. I hope some of our members who have used these meds will be able to answer this question for you. Also, this might be a good question to ask the NETs support group on the first Thursday of each month.

The fact that the primary NET is unknown is a common problem. Have you had a Gallium 68 scan to try to determine where the primary is located?

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@hopeful33250

Hello @sophiarose

Personally, I have never taken either octreotide or lanreotide so I do not know the difference between the two. I understand that one is easier to inject than the other. Here is an article from the National Library of Medicine about the two different medications, https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6643159/. I hope some of our members who have used these meds will be able to answer this question for you. Also, this might be a good question to ask the NETs support group on the first Thursday of each month.

The fact that the primary NET is unknown is a common problem. Have you had a Gallium 68 scan to try to determine where the primary is located?

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Thank you

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Hello, I’m not really sure if I’m doing this right, but I’ll try. My husband had surgery in March for an insulinoma and was doing very well until Aug. 9th when his blood sugar plummeted. He’s been in the hospital since then but have an appt. at Mayo Sept14th. He’s flying up there in an air ambulance and I’ll drive up. We have no idea what to expect, but have faith in the doctors there (faith in Jesus first, tho). I just wanted to see what this group is like…it seems very friendly and welcoming.

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Think positive thoughts as you travel to the Mayo! I'm sure they will work diligently to help your husband! Sending big hugs!

Sandi Barkan

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