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Neuroendocrine tumors

Neuroendocrine tumors, cared for close to home by one team.

Neuroendocrine tumors are a diverse group that can grow slowly over years or behave more aggressively. Treatment is highly individualized, and our oncologists tailor it to the tumor's grade, location, and whether it produces hormones.

How we approach it

Tailored to tumor behavior

Slow-growing tumors may be watched or treated with specialized medication; faster-growing ones need more

Specialized therapies

Options can include hormone-blocking medication, targeted therapy, and specialized nuclear treatments

Hormone-symptom control

When a tumor produces hormones, controlling those symptoms is part of the plan

What the workup looks like

1
Confirming and grading

A biopsy confirms the tumor and measures how quickly it's growing — its grade — which drives the whole plan.

2
Specialized imaging and labs

Dedicated scans, such as a DOTATATE PET, and hormone-related blood tests locate the tumor and gauge its activity.

3
Matching treatment to behavior

Because these tumors range from very slow-growing to aggressive, the plan is tailored to your tumor's grade and any symptoms.

Common questions

What is a neuroendocrine tumor?
It's a tumor arising from hormone-producing cells found throughout the body — most often in the digestive tract, pancreas, or lungs. Behavior varies widely.
Are these tumors cancerous?
They range from slow-growing to aggressive. 'Grade' describes how quickly a tumor is dividing and helps guide treatment.
What is carcinoid syndrome?
Some neuroendocrine tumors release hormones that cause flushing, diarrhea, or other symptoms. Specific medications can control them.
Do these need treatment right away?
Not always — some are watched closely. The plan depends on the tumor's grade, size, location, and symptoms.

This page is general information, not medical advice for your specific situation. Every diagnosis — and every patient — is different. Bring your questions to your care team.