You may not have heard of gastroenteropancreatic neuroendocrine tumors, or GEP-NETs. These are tumors that develop in the gastrointestinal tract. They are formed from neuroendocrine cells, which produce hormones and control many bodily functions.
“We’ve developed multiple therapies over the last two decades which are [generally] well tolerated and very effective,” says Kimberly Perez, MD, Medical Oncologist with Dana-Farber Cancer Institute in Boston.
What are neuroendocrine cells?
Neuroendocrine cells function as relay centers, meaning that they tell your body what to do in response to environmental stimuli. When neuroendocrine cells become abnormal and grow at an out-of-control rate, that’s when they become cancerous.
Rather than sending signals in response to stimuli, cancerous neuroendocrine cells will send random signals.
What is carcinoid syndrome from a GEP-NET?
Sometimes this signaling causes symptoms of carcinoid syndrome, explains Perez. Carcinoid syndrome can include symptoms such as:
Diarrhea
Flushing
Stomach pain
Racing heart
Low appetite
Swelling
If you do experience any symptoms of carcinoid syndrome, make sure to tell your care team so that they can help treat it.
What should you know about GEP-NET treatment?
While it’s completely normal to feel overwhelmed after a GEP-NET diagnosis, Perez says that there are many great treatment options available.
“We’ll always be looking for better options for you to help manage your disease and make sure that your quality of life is maintained and improved as much as possible,” she says.
Kimberly Perez, MD, is a Medical Oncologist at the Dana Farber Cancer Institute in Boston, MA.
References
American Cancer Society. (2018). Treatment of gastrointestinal carcinoid tumors, by extent of disease.
Cives, M., et al. (2018). Gastroenteropancreatic neuroendocrine tumors. CA: A Cancer Journal for Clinicians.
Pandit, S., et al. (2023). Carcinoid syndrome. StatPearls.
U.S. Food & Drug Administration. (2018). FDA approves new treatment for certain digestive tract cancers.
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