Octreotide Injections - Skipping One or More?
Following completion of PRRT treatment, my wife has been receiving monthly octreotide (Sandostatin LAR) injections.
She will be out - of -town when the next injection is to be done.
Question:
Has anyone skipped an injection (s)?
If so, did this result in negative impacts?
All comments will be appreciated.
Thanks,
Mark
Interested in more discussions like this? Go to the Neuroendocrine Tumors (NETs) Support Group.
@markmark007
Thank you for your prompt reply. Wonder if PRRT is the first treatment option prescribed for your wife instead of the more common octreotide injection?
All the best to you and your wife.
Just adding a little update on my experience with PRRT to Mark's response. I completed my last (of 4) PRRT treatments in January 2022--so this January will be 2 years since completion. I got both tumor shrinkage and stability and some of the shrinkage was significant. I've continued with blood work and scans at Mayo Arizona every 6 months and I just completed a visit a few weeks ago. I continued to see some shrinkage for about a year after completion and stability after that. Some of my blood values were moderately lower than normal after treatment and gradually came back up over time. There are still a few results that are at the very low end of normal or even sometimes just out of normal range. My doctors say that is pretty normal for this treatment and not something to be overly concerned about. Keep up a good nutrition program and as much exercise as you can do--both really help to get everything back close to normal and reduce any lingering fatigue. Wishing all good results--it was really effective for me.
Markmark007, I have not been part of this particular conversation, but just now read your comments about expectations for PRRT. I agree with everything you said and confirm that has been my experience. I completed 4 rounds of PRRT (3 were done with half dosage due to some unusual side effects) at Mayo in October 2021. I have had two scans since with the results being “stabilization of disease”. I have another Gallium 68 scheduled in January. In the meantime, I continue to get my Sandostatin LAR injections every 28 days which I will have been on since April 2018. I have some ups and downs, but I basically just go on with my life.
When diagnosed in March 2018, I told my oncologist that I had decided to view this as being similar to a chronic illness you manage. He totally agreed.
The best to you all.
Hello Phyllis:
Many thanks for sharing your experiences.
We are all in this together -
Mark
Kwan:
Based on our own experiences dealing exclusively with NET's:
There may be cases in which neither octreotide nor lanreotide are effective for on - going treatment e.g. tumor growth is not suppressed when using these therapies. In cases such as this, PRRT maybe be the best choice - certainly the patient's medical team & recommendations from a tumor board are important to receive and to define the best therapy path going forward.
Mark
I have Malignant Neuroendocrine Tumors of the Lung and have been in treatment with Sandostatin LAR every 28 days since November 2022. It has helped with my coughing, and the tumors remain the same size. However, the side effects of Sandostatin LAR are significant, and I felt my body needed relief. I conferred with my Oncologist, and while he mentioned this treatment would be continuous, I skipped a dose under his supervision to see whether the side effects would subside. He suspects malabsorption and will treat it accordingly.
The side effects did reduce during the relief, except the constant coughing returned, and shortness of breath escalated. I have since then had two injections, and the side effects resurfaced. Sometimes, I do not know what is worse: the treatment’s side effects or the disease itself. Everyone is different, so what is affecting me may not be affecting anyone else.
I pray for everyone's improvement and strive to manage this journey.
Many Blessings.
Thanks for sharing -
God Bless you!!
Mark
@kjstein
Thanks for sharing your experience. It makes going forward with the treatment more optimistic. Is the shrinkage more visible from ctscan and not from petscan dotatate?
My son is following the Mediterranean diet. He tries to avoid beef which to me is a good source of protein to help with blood count.
All the best to you.
@markmark007
Thanks for sharing your experience. My son was put on Everolimus for 2 weeks after an unsuccessful operation. Then he was prescribed PRRT treatment. He is now scheduled for the third treatment of PRRT. All we can do now is to wait for the response. Meanwhile he is feeling good. Not much side effect except the blood counts are low.
All the best to you and your wife.
@phyllisden
Thanks for sharing your experience. If PRRT helps to " stabilise the disease" in my son's case, it's one big step forward.
Do you avoid eating beef?
Best wishes to you.