Neuroendocrine Tumors Clinical Trial
— GALTEPOfficial title:
Development of an Innovative Gallium 68 Radiolabeling of DOTATOC (68Ga-DOTATOC) for PET-CT Imaging of Neuro-endocrine Tumors and Preliminary Clinical Evaluation
Verified date | August 2017 |
Source | University Hospital, Bordeaux |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Observational |
Through the investigators involvement in an international consortium, the investigators had the opportunity to acquire a new type of synthetizer for the radiolabelling of such tracers. The investigators propose in this project to develop on their site, the radiosynthesis of 68Ga-DOTATOC and to evaluate prospectively the diagnosis of neuroendocrine tumors, compared with the current imaging OctreoScan®. The objectives of this project are: - to validate the radiosynthesis of 68Ga-DOTATOC on their site with a new synthetizer - and clinically evaluate, through a prospective preliminary study, the diagnostic accuracy of PET-CT with 68Ga-DOTATOC in comparison with other standard imaging examinations.
Status | Completed |
Enrollment | 20 |
Est. completion date | January 2015 |
Est. primary completion date | December 2014 |
Accepts healthy volunteers | No |
Gender | All |
Age group | 18 Years and older |
Eligibility |
Inclusion Criteria: - Patients over 18 years - Patient who is suspected of endocrine tumors according to symptomatology, biology or imaging or pathological context (multiple endocrine neoplasia type 1) - initial staging: this includes research multifocal disease or locoregional or metastatic extension if well-differentiated neuroendocrine tumor (grade 1 et/ou 2) - Search of the primary tumor, especially in the case of the inaugural discovery of metastases - staging of a known recurrence - Search occult recurrence or suspicion of recurrence (clinical, laboratory, imaging doubtful) - Patient who have received in a lower range than 2 months of cervico-thoraco-abdominal-pelvic CT and scintigraphy in OctréoScan® - Patient who have signed an informed consent - Patient affiliated or beneficiary of regime of social security of a Member State of the European community Exclusion Criteria: - Patient with another evolutive cancer disease and/or treated for less than 5 years - Pregnant or lactating woman - Premenopausal woman without effective contraception (estrogen-progestin or intrauterine contraceptive device) - Patient unable to give their free and informed consent - Persons placed under judicial protection |
Country | Name | City | State |
---|---|---|---|
France | CHU de Bordeaux | Bordeaux |
Lead Sponsor | Collaborator |
---|---|
University Hospital, Bordeaux |
France,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Evaluation of PET imaging | The diagnostic performance of PET-CT will be calculated and compared with other standard exams as the gold standard histology and clinical follow-up. | Inclusion (day 0) | |
Secondary | Reproducibility | The reproducibility of the new method of radiolabelling will be evaluated by the number of failed syntheses | Inclusion (day 0) | |
Secondary | Tolerance | Tolerance of the tracer will be assessed by the collection of possible side effects | Inclusion (day 0) and until end of follow up (day 28) | |
Secondary | Impact on the therapeutic management | The impact on the therapeutic management of patients will be studied by the analysis of questionnaires with or without taking into account, the results of the PET-CT with 68Ga-DOTATOC. | End of follow up (day 28) |
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