Clinical trial · Observational
Explore the Clinical Value of 68Ga-DOTANOC PET/CT and 18F-FDG PET/CT in Neuroendocrine Neoplasms
A Prospective Exploration in the Clinical Value of 68Ga-DOTANOC PET/CT and 18F-FDG PET/CT in Neuroendocrine Neoplasms
NCT03288597CI-TRIAL-00029611unknownClinicalTrials.gov clinicaltrialsProvenance
- Source
- ClinicalTrials.gov
- Retrieved
- Sep 8, 2026
- Layer
- normalized (units and labels harmonized; values unchanged)
- Run
- ING-CLINICALTRIALS-20260908-000001
Summary
Brief summary (as posted)
68Ga-DOTANOC and 18F-FDG PET/CT have important values in the staging and clinical treatment of neuroendocrine tumors. Retrospective studies suggest that the positivite rates and SUVmax of dual imaging associated with pathological findings and prognosis. The study was designed to confirm thet clinical values of dual imagings for neuroendocrine tumors.
Conditions
Conditions (1)
Free-text conditions as registered, with the CancerIndex entity they were reconciled to and the match type.
| Condition (as posted) | Mapped entity | Match | Confidence |
|---|---|---|---|
| Neuroendocrine Tumors | Neuroendocrine Tumor | ONTOLOGY_EXACT | 0.90 |
Interventions
Interventions (2)
| Intervention | Type | Mapped drug | Match |
|---|---|---|---|
| 68Ga-DOTANOC PET/CT and 18F-FDG PET/CT in NEC | Radiation | — | UNRESOLVED |
| 68Ga-DOTANOC PET/CT and 18F-FDG PET/CT in NET | Radiation | — | UNRESOLVED |
Design
Arms and outcomes
Arms (2)
- label
- A: advanced and metastatic neuroendocrine tumors
- description
- Advanced and metastatic neuroendocrine tumors receive syestematic treatment
- interventionNames
- Radiation: 68Ga-DOTANOC PET/CT and 18F-FDG PET/CT in NET
- label
- A: advanced and metastatic neuroendocrine carcinomas
- description
- Advanced and metastatic neuroendocrine carcinomas receive syestematic treatment
- interventionNames
- Radiation: 68Ga-DOTANOC PET/CT and 18F-FDG PET/CT in NEC
Primary outcomes (1)
- measure
- The correlation between the positive rate and SUVs of 68Ga-DOTANOC PET/CT and 18F-FDG PET/CT and treatment response
- timeFrame
- 3 years
Secondary outcomes (2)
Eligibility
Eligibility (as posted)
- Sex
- All
- Minimum age
- 18 Years
Show eligibility criteria text
Inclusion Criteria: 1. sign written informed consent form 2. age ≥ 18 years 3. pathologically confirmed neuroendocrine, Ki67\>=10%; 4. ECOG 0-1; 5. No prior antitumor treatment with chemotherapy targeting regimens for neuroendocrine carcimomas, no more than 2 systematic treatment for neuroendocrine tumors; 6. Unresectable disease; 7. At least 1 measurable lesion (only 1 measurable lymph node lesion is excluded) (routine CT scan \>=20mm, spiral CT scan \>=10mm, no prior radiation to measurable lesions); 8. Predicted survival \>=3 months; 9. Negative serum or urine pregnant test within 7 days prior to randomization for child-bearing age women; 10. Sexually active males or females willing to practice contraception during the study until 30 days after end of study. Exclusion Criteria: 1. In the process of antitumor therapy with effective response; 2. Refuse to accept PET/CT; 3. Pregnant or nursing, or sexually active males or females refuse to practice contraception during the study until 30 days after end of study; 4. Person with no capacity (legally) or inappropriate to continue study treatment for ethics/medical reasons;
References
Publications (0)
Data not yet available
No reference posted for this study.