Interested in hearing people's experiences with PRRT
Sorry if this has been discussed before, but I was interested in hearing peoples experience with PRRT (Peptide Receptor Radionuclide Therapy)? I live in Georgia and have an appointment at Mayo in Jacksonville next month and I was wondering if this was something they would discuss...
Interested in more discussions like this? Go to the Neuroendocrine Tumors (NETs) Support Group.
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Hello @gapsc,
As it has been several months since you last posted, I was thinking about you and wondering how you are doing.
Will you post an update at your convenience?
@klpetts Hello Karin,
Last month you indicated that you would be starting some oral chemo treatments. Have you started those meds already?
How are you feeling? Are you still working?
@klpetts Hello Karin
I'm disappointed to hear that the results of your tests were not more favorable. After going through the rigors of PRRT, I'm sure must feel discouraged as well.
What has your doctor said regarding the Xeloda and Temodar? Are these meds often used to treat advanced cancer? When will you start this treatment?
I hope that this treatment offers potential for you. Will you post an update and let me know how you are doing?
Thanks for checking in on me. On March 17 I had lad work and a Nuc Med PET CT, results were given to me on Monday and were not in my favor. Therefore the PRRT treatment is no longer working for me. Last week (Mar 24) I had a Nuc Med PET CT and lab work done. Tumor count has gone back up (was 158 now 951) and the CT showed progression of the cancer, is now in many more places. I will be starting an oral chemotherapy treatment next week in addition to the injection that I get every four weeks. The two oral chemotherapy treatments that I will be starting; Xeloda and Temodar. Karin
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1 ReactionHello @klpetts,
I hope you are feeling better. As I recall, when you last posted you indicated that you would be having a follow-up CT in March. Has that been scheduled yet? I look forward to hearing from you. Will you post an update when it is convenient for you?
Hello @gapsc
I hope that by now you have had your COVID vaccine. Did it go well for you without too many side effects?
When do you anticipate starting PRRT?
Hello @gapsc,
I am also a patient with NETs. I had my first COVID vaccination last week, however, I do not have any metastasis. As @colleenyoung, suggested, you should definitely talk with your oncologist regarding this vaccine, especially the coordination of the vaccinations with your PRRT treatments.
I will be having surgery on 2/4 (not NETs related) and the hospital pre-surgery screener suggested that I wait an extra week for the 2nd vaccination Timing is always important with these types of treatments/procedures.
If you are comfortable sharing more about your history with NETs: how long ago were you diagnosed with NETs; what treatment have you had so far?
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1 ReactionHi @gapsc, these are good questions to ask your oncologist regarding the COVID vaccine and its possible interference with the effectiveness of PRRT or PRRT disrupting the effectiveness of the vaccine. I would ask not only about the first shot a week before PRRT, but also remind them that a second shot is required.
Gapsc, is the metastases a recent diagnosis?
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1 ReactionI guess this is the end of the run on PRRT. I have lung nets with metastases. I am scheduled for Prrt. Also on list to get covid vaccine a week before. Any one have experience with getting the vaccine and interference with PRRT? Do I get it or wait for full immunity.
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1 ReactionHello @klpetts,
It's so good to get an update from you. I'm glad to hear that your tumor marker count was down by that much over the past year. I'm glad that you are feeling good. Tiring easily is probably to be expected?
I hope that your next blood test and PET CT in March show more improvement.
I look forward to hearing from you again.
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