Study of PRRT in Metastatic, World Health Organization (WHO) Grade 1 or 2, SSTR Positive, GEP-NET Who Are Candidates for Cytoreductive Surgery

Recruiting Phase 1 Interventional Study
Gastroenteropancreatic Neuroendocrine Tumor
No Placebo Group Every participant receives an active treatment — no one gets a placebo.
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At a Glance
Age
18 and older
Sex
Any
Trial phase
Phase 1
Study type
Interventional
Purpose
Treatment
Participants needed
10 (estimated)
Sponsor
Stanford University · Other
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About This Trial
The purpose of this study is to learn about the feasibility and safety of using Peptide Receptor Radionuclide Therapy (PRRT) before and after surgical removal of a tumor. PRRT treatment is based on the administration of a radioactive product, 177-Lu DOTA-0-Tyr3-Octreotate (Lutathera®) and its use before and after surgery is thought to increase the overall survival benefit for patients with SSTR-po…
Trial Locations
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Eligibility Criteria
Inclusion Criteria: 1. Metastatic gastroenteropancreatic NET with lymph nodes or liver metastases only. 2. WHO Grade 1 or 2, Ki 67 ≤ 20% (to be confirmed at Stanford) 3. Must be a candidate for cytoreductive surgery with the goal of R1 resection as determined by a multidisciplinary tumor board disc…
Contacts

gitrialeligibility@stanford.edu gitrialeligibility@stanford.edu

(650) 498-7757

gpineda@stanford.edu

CONTACT

gitrialeligibility@stanford.edu gitrialeligibility@stanford.edu

(650) 498-7757

gitrialeligibility@stanford.edu

CONTACT