Neuroendocrine Tumors

What is a Neuroendocrine Carcinoid Tumor?

A neuroendocrine tumor is cancer that forms in the lining of the gastrointestinal tract. It can include neuroendocrine carcinoma and neuroendocrine cancer of the Spleen, and tumors in pancreatic eyelet cells.

Gastrointestinal carcinoid tumors grow slowly and generally appear in the appendix, small intestine, and rectum. Often, more than one tumor develops in the small intestine. A diagnosis of a gastrointestinal carcinoid tumor increases your risk of developing another cancer in the digestive system.

Treatment for Neuroendocrine Carcinoid Tumors

Treatment for gastrointestinal carcinoid tumors initially involves surgery to remove the tumor. If the disease spreads to other parts of the body, additional treatment may given, including:

  • Surgery to bypass or remove part of a tumor blocking the small intestine.
  • Chemotherapy, which may include chemoembolization.
  • Radiation therapy, sometimes with radioisotopes such as radioactive iodine (I131).
  • MIBG (metaiodobenzylguanidine)therapy.
  • Biologic therapy and/or hormone therapy.

See National Cancer Institute information on
Gastrointestinal Carcinoid Tumor
Patient Success Stories
Request an Appointment
Find a Clinical Trial

Find a Clinical Trial

Find a Clinical Trial

Benefit from new cancer treatments
Read more »

Resources and Education for Patients and their families

The Resource and Education Center

Cancer Questions?
Call 215-214-1618
or send a secure e-mail.
Connect with a cancer education specialist for answers to your
cancer-related questions.
Learn what the REC has to offer ยป