I recently had surgery to remove NET in small intestine
They did a rt hemicolectomy and small bowel resection. They also did a wedge resection of my liver. They removed all of the tumor. Liver pathology came back clear. What concerns me is 7 out of 20 lymph nodes came back positive and they are telling me there is no treatment. They said high reoccurence and to just do scans and lab work every 6 months. Is this true no treatment just wait for reoccurence???
--Well-differentiated neuroendocrine tumor, grade 2.Tumor is 1.8 cm in greatest dimension.
Lymphvascular invasion is identified.
Perineural invasion is identified.
Number of lymph nodes examined: 20.
Number of lymph nodes involved: 7.
Maximum size of metastasis (glass slide measurement): 4 mm
Interested in more discussions like this? Go to the Neuroendocrine Tumors (NETs) Support Group.
Believe it or not that is exactly what my Oncologist told me. Pathology Report showed 8 Lymph Nodes out of 22 positive for NET. 75 percent possibility of reoccurrence. Scans and blood work every 6 months.
Stay positive, I had 15 years ago nec in my small intestine, surgery sucesfully but secondary effect Diarrea, since 4 years ago found liver cáncer inoperable, treatment lanreotide injection per month and 4 cicles of PRRT LUTHATERA-177 cancer stable, two years ago breast cancer small tumor test.. estrogen positive all hhis cancers was about hormonal teraphy. You can found experts in PRRT. I am in Houston and Excel Diagnostics apply me 4 doses of Luthatera, finish 2 years ago, now is a little bit grow one tumor and have two more sessions of Luthatera, but I am waiting for prrt Alphamedix to be approved for FDA. But I never give up snd I feel very well
Yes, it is essential to have CT Scans every month and then every 6 months, and GALLIUM 68 scan, a lab test, and Possible lanreotide injection every month; you have to look for an oncologist expert in Neuroendocrine tumors. Chemotherapy does not work in this kind of cancer
Did they remove the cancerous lymphnodes? I had SI NET removed along with 7 lymphnodes removed and GB. Now Lanreotide every month and MRI every 3 months. Feeling good.....2 yrs out. I wish you well.🙏
Yes, the 8 Lymph nodes were removed. No injections planned at this time. Scans and blood work only
Where did you learn chemo doesn't work for this kind of cancer?
In general terms it seems the slower your cancer grows, the less effective chemo would be. Therefore, many NETs patients grade 1 or 2 are not candidates for chemotherapy.
I believe you can have a completely clear PET scan and still have Neuroendocrine cancer. Dividing cancer cells are very small. There is no known cure for NETs. My Oncologist made a great point when he said " I don't use terms like cancer free, that's not real". On a positive note, it can be very slow growing and there are drug treatments that are affective in stalling this cancer for many.
Found this info on the net about using chemo at http://www.everydayhealth.com
Chemotherapy Chemotherapy uses drugs to kill cancer cells. It isn’t generally used for tumors that are grade 1 or 2, says Kim, but for the more aggressive grade 3 tumors. According to a study, more research needs to be done on chemotherapy’s effectiveness in grade 3 tumors, particularly new chemo combinations or chemotherapy combined with other treatments. Among the many chemo drugs used to treat GEP-NETs are streptozocin (Zanosar), doxorubicin (Adriamycin), etoposide (Vepesid), dacarbazine (DTIC-Dome), fluorouracil (Adrucil), and cisplatin (Platinol). Some of these drugs are given in combination.
I had chemo I am grade 2 ki-67 7% stage 4 to liver as far as I know it s very common first treatment definitely not a cure though.
Where can I read the study that you referenced? Thanks
This is the article I found and referenced. I don't know about the actual study.
https://www.everydayhealth.com/gastroenteropancreatic-neuroendocrine-tumors-gep-nets/