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Somatostatin Receptor Imaging in NPC, EBV Related Cancers

Somatostatin Receptor Imaging in Nasopharyngeal Cancer, Epstein-Barr Virus (EBV) Related Cancers and Other Rare Tumors

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT05581550
Enrollment
15
Registered
2022-10-14
Start date
2020-06-29
Completion date
2025-07-17
Last updated
2025-07-20

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Epstein-Barr Virus Related Carcinoma, Nasopharyngeal Cancer

Keywords

Somatostatin, EBV, NPC, Rare Cancer

Brief summary

The study aims to describe the avidity of somatostatin receptors in locally advanced, metastatic and locally recurrent nasopharyngeal cancer (NPC) and to determine the proportion of NPC patients with high somatostatin receptor density that may benefit from future somatostatin targeted therapeutic trial plans. The investigators also aim to determine the presence of somatostatin receptors in other EBV related cancers.

Interventions

RADIATIONFDG-PET

Patients will be fasted for 6 hours prior to intravenous injection of 370MBq +/- 10% (18)F-fluorodeoxyglucose. Scanning will be performed at an interval of at least 60 minutes following the injection.

RADIATIONGalium-68 DOTATATE

200MBq +/- 10% Galium-68 DOTATATE will be injected intravenously. Scanning will be performed approximately 60 minutes after the injection.

Sponsors

National Cancer Centre Research Fund
CollaboratorUNKNOWN
National Cancer Centre, Singapore
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
DIAGNOSTIC
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
21 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Locally advanced, metastatic or locally recurrent NPC that are going for FDG PET as part of their investigations * Patients that have gone for Ga-68 DOTATATE imaging before are eligible for repeat imaging * Histologically confirmed NPC * Above 21 years of age

Exclusion criteria

* Patients below 21 years of age * Pregnant and breast feeding ladies

Design outcomes

Primary

MeasureTime frameDescription
Amount of tracer uptake in the tumour lesions of NPC patientsFrom time of tracer injection to time the scan is performedThe maximum standardized uptake values (SUVmax) will be measured. If the average SUVmax of all the lesions is more than 10, the patient will be considered to have an overall high somatostatin receptor density.

Secondary

MeasureTime frameDescription
Amount of tracer uptake in the tumour lesions of patients with EBV related cancersFrom time of tracer injection to time the scan is performedThe maximum standardized uptake values (SUVmax) will be measured. If the average SUVmax of all the lesions is more than 10, the patient will be considered to have an overall high somatostatin receptor density.
Number of somatostatin receptors in patient biopsy samplesUpon signing the informed consent form
Amount of somatostatin circulating tumour cells in patient blood samplesAt the time of scan

Countries

Singapore

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026