← Return to Anyone had plexus nerve block for cancer pain?

Discussion

Anyone had plexus nerve block for cancer pain?

Pancreatic Cancer | Last Active: Feb 25 2:24pm | Replies (28)

Comment receiving replies
@donnarushing55

Has anyone been advised to use a celiac plexus nerve block for back and upper abdominal pain caused by a neuroendocrine tumor in the tail of the pancreas? I am early into a clinical study at Mayo (FL) with octreotide injections every 15 days and I am scheduled for a scan in March to hopefully measure progress in arresting any possible growth. But it is my understanding that octreotide does not reduce current tumor size, only affecting further progression.

I hesitate to overuse ibuprofen (or stronger pain medicine) and the only other thing my oncologist has suggested is a nerve block. Have others successfully used this when surgery is not an option? I have sought out two opinions and both oncologists feel my pain is coming from pressure on a nerve - and with metastasizes to both lobes of my liver and a lymph node, neither would offer surgery. Fortunately, upper abdominal and middle back pain are the only symptoms I routinely experience. Knowledge of nerve blocks as common practice would be comforting and very much appreciated. I'm feeling quite alone as I've not seen anything about it posted in this group.

I've been advised (by well-meaning friends AND the docs) not to let this diagnosis rob me of my daily joy and experience a full life but it's really hard when pain is a constant reminder of a tumor in my pancreas (albeit non-functioning and slow growth). Can something relatively simple as a nerve block be helpful and if so, is this a sustainable option for the long haul as I'm only 68 and otherwise healthy?

Jump to this post


Replies to "Has anyone been advised to use a celiac plexus nerve block for back and upper abdominal..."

Interesting my husband supposably has a Pnet in his tail of his pancreas and has had different measurements but neither has measure up to greater than 2 for them to do surgery. They (Hopkins and Mayo in Minnesota) have offered no treatments but wait. He has extreme pain after eating seems like the pressure of food in his stomach puts pressure on nerve/tumor. They recommend a nerve Bloch as well at our local health system. He has had 2 TAP blocks but not celiac plexus from my understanding. The 1st one worked about a 1.5 weeks. The 2nd he had done on 1/23 and so far he has had 1 flare up but it seem to subside and then went away. He does still have constant indigestion. They claim his is non functioning but I am not 100% sure they are correct I feel like they just haven’t caught his active when they have tested him. I am curious what your history of symptoms and progression of your journey has been. Ours has been frustrating as my husband’s quality of life has been not good because of the constant pain and occasional diarrhea flare ups which can be bad.

@donnarushing55 and @tinerobison, I moved your questions about celiac plexus nerve block related to pancreatic NETs to this existing discussion:

- Anyone had plexus nerve block for cancer pain?
https://connect.mayoclinic.org/discussion/celiac-plexus-block-1/
I did this so you can read previous messages and connect easily with others like @lulusmom @granite @beatrixlee @lizduffey @joylynnlove @stageivsurvivor and others.