Diagnosed with Stage 4 pancreatic neuroendocrine metastasized to liver
Hi everyone. I am new to the group and wondered what kinds of symptoms others with Pnet go through. I was diagnosed just under a year ago and began the lanreotide infusion shot this past October. I went into my regular doctor last May for what I thought was a gall bladder infection. My doctor sent me in for a full abdomen CT and found a 3 cm mass on the tail of the pancreas. At the time my doctor told me we need to look at the mass first before looking into the gall bladder. After several PT scans and biopsies they can see small tumors covering my entire liver the largest being 1.1 cm. Since surgery was not an option, I started on the infusion. My nausea did not go away so I went back in to see about my gall bladder. Since then I feel 25 times worse. I’m exhausted all the time, very little appetite but no real weight loss, depression from having to rely on my family and pain around the pancreas and liver. I am grade 2 well functioning stage 4. Any suggestions would be greatly appreciated
Interested in more discussions like this? Go to the Neuroendocrine Tumors (NETs) Support Group.
Thank you so much for your concern. We’re glad your doctors have given you a good prognosis. Jim’s CAP/TEM treatment does include capecitabine and temozolomide along with the lanreotide injections. Take care.
Hello @gsm13161,
I see that you mentioned genetic testing and said that, "it can assist future treatment decisions." Is genetic testing something that you have done?
As I have not heard about genetic testing being used for the treatment of NETs, I would be interested in knowing if the testing helped determine the treatment that you are now having. Please share as you are comfortable doing so.
Yes, I did have genetic screening not long after the primary tumor was resected in late 2016. The endocrinologist thought it would be a good idea so she referred me to a genetic counselor at City of Hope. It was discovered I had a mutation in sdha which at the time they felt was good. They were hoping not to find anything in sdhb which is widely considered to be a more aggressive subtype of Pheochromocytoma/ Paraganglioma. However they are recently finding in other countries where more research is being done on these diseases that sdha can behave similarly to sdhb in that it can metastasize early and exhibit suboptimal response to conventional treatment strategies. I don't believe the testing has greatly influenced the dr.s decisions as much as the serial imaging that is performed but I do believe it is something they are aware of and may impact any changes in the regimen I am receiving going forward.
Hope that helps
I appreciate that information, @gsm13161. That is very interesting. I've learned so much from this forum and this is a new piece of information.
just wondering how your wife is doing with the CAPTEM. My husband just started his course of CAPTEM this past Saturday.
Good luck today kim. Waiting for the results can be quite nerve wracking.
Thanks for asking. She completed her first course and is about to start round 2. Despite some fatigue, gas/bloating, and a need to get calories to maintain weight she is doing quite well. Nausea has not been a problem nor have some of the other reported side effects. She has been able to maintain her exercise schedule and some of her work.
I wish you and your husband the best in your treatment.
@tomatlanta I'm praying for healing and thank u you so much for this information for it is very helpful.
Thanks! We got a CT scan earlier this week and met with our cancer team today. It did show signs of some growth in the liver, not to worry, getting a MRI to confirm in 2 weeks, then the team will meet on the best course of action. Other than the challenges of the diabetes, all is going well. Whatever is growing will be addressed by the procedure which will continue this long path of keeping NET at bay. I’m wondering how everyone is doing that had their tail of pancreas removed? What challenges have you incurred and what has worked in dealing with this new normal in our life’s.
Have they suggested prrt therapy?