Radioactive drug plus surgery: new hope for gut tumors?

NCT ID NCT04609592

First seen Sep 30, 2025

Summary

This pilot study tests whether giving a radioactive drug (Lutathera) before and after surgery is safe and feasible for people with advanced gastroenteropancreatic neuroendocrine tumors (GEP-NETs). The drug targets tumor cells and delivers radiation directly. Ten participants will receive two doses before surgery, then two more after, to see if this combination can improve outcomes without causing serious complications.

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This is a summary of the original study . Summaries may miss details or leave out important information. Before applying or accepting participation, make sure you have read and understood the full study. Curemydisease.com takes no responsibility whatsoever for anything missed, misunderstood, or acted upon as a result of our summary — we know it does not capture everything.

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Contacts and locations

Study contacts

  • Contact

    Phone: •••-•••-•••• Email: •••••@•••••

  • Contact

    Phone: •••-•••-•••• Email: •••••@•••••

Locations

  • Stanford Cancer Institute Palo Alto

    RECRUITING

    Stanford, California, 95304, United States

    Contact Email: •••••@•••••

    Contact

What this could mean

Our plain-language read of the trial. This is informational only — not medical advice or a prediction.

Active substance

Lutetium Lu 177 dotatate (Lutathera) and Gallium 68 Dotatate

What this could lead to

If successful, this approach could improve survival for people with advanced neuroendocrine tumors by combining targeted radiation with surgery.

What could go wrong

This is a very early, small pilot study with only 10 participants. The treatment involves radiation and major surgery, which carry risks like organ damage or surgical complications. It may not prove effective in larger trials.

Conditions

The condition(s) this trial relates to.

digestive system neuroendocrine neoplasm digestive system neuroendocrine tumor, grade 1/2

As listed by the trial registrant

The condition terms exactly as the trial's registrant entered them.