Phase
Condition
Carcinoid Syndrome And Carcinoid Tumours
Abdominal Cancer
Digestive System Neoplasms
Treatment
Peptide Receptor Radionuclide Therapy
Clinical Study ID
Ages > 18 All Genders
Study Summary
Eligibility Criteria
Inclusion
Inclusion Criteria:
> 18 years of age
Diagnosed with gastroenteropancreatic primary NET and has consented to undergo PRRTper the treating physician. Specifically:
Will consider other primaries on a case by case basis if dotatate scan (+) andmeet all other criteria.
Metastatic or Locally Advanced AND Inoperable
Clear disease progression on Octreotide over less than 3 years (RECIST 1.1)
Presence of disease within 24 weeks as identified by PET/CT scans with Ga-68DOTATATE reporting the Krenning score for low-grade NET and/or PET/CT scanswith FDG for transformation to high-grade NET
Well differentiated on path - Ki67 < 20%
Octreotide positive on pathology (if not documented, acceptable if PET/CTimaging shows lesions with Ga-68 DOTATATE uptakeLabs:
Cr. <1.7
Hgb >8
WBC >2K
Plt >75K
Bili < 3x normal limit
No Octreotide within 30 days of administration.
Willing and able to comply with the protocol requirements
Able to comprehend and sign the Informed Consent Form in English.
Exclusion
Exclusion Criteria:
- Do not meet the Study Inclusion Criteria laid out in section 6.3
Study Design
Study Description
Connect with a study center
Clinical Research Institute at Methodist Health System
Dallas, Texas 75203
United StatesActive - Recruiting
Methodist Dallas Medical Center
Dallas, Texas 75203
United StatesSite Not Available

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