Skip to content

Application of Al18F-octreotide PET/CT in Tumors With Positive SSTR Expression

Application of Al18F-octreotide PET/CT in Tumors With Positive SSTR Expression

Status
Recruiting
Phases
Phase 2Phase 3
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT05749289
Enrollment
400
Registered
2023-03-01
Start date
2022-12-20
Completion date
2029-12-20
Last updated
2026-04-06

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

Conditions

SSTR Positive Tumors

Brief summary

This is an open-label whole-body PET/CT study for investigating the value of Al18F-octreotide PET/CT in patients with SSTR positive tumors

Detailed description

Octreotide is an artificial replacement for the natural growth hormone inhibitor in humans. It is a small peptide hormone consisting of 14 amino acids and is widely distributed in neuroendocrine cells, with the highest density in the brain, peripheral neurons, endocrine pancreas and gastrointestinal tract. Under pathological conditions, some tumour cells show overexpression of growth inhibitory receptors, such as endocrine tumours of the pancreas, pituitary adenomas, pheochromocytomas, paragangliomas, carcinoid tumours, medullary thyroid carcinomas, small cell lung carcinomas Hepatocellular carcinoma, and meningioma. Therefore, the sensitivity and specificity of octreotide imaging is high. This study will provide a visual, reproducible and non-invasive imaging method for the diagnosis of SSTR positive tumors through Al18F-octreotide PCT/CT imaging, providing an intuitive and clear imaging basis for clinical diagnosis, differential diagnosis and treatment, contributing to the development of medicine and science in the field of positron imaging.

Interventions

DRUGAl18F-octreotide

Al18F-octreotide I was injected into the patients before the PET/CT scans

Sponsors

Cancer Institute and Hospital, Chinese Academy of Medical Sciences
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
DIAGNOSTIC
Masking
NONE

Eligibility

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

Inclusion criteria

* Patients with suspected or clearly diagnosed SSTR positive tumors * signed written consent. * Willing and able to cooperate with all projects in this study.

Exclusion criteria

* pregnancy; * breastfeeding; * any medical condition that in the opinion of the investigator may significantly interfere with study compliance.

Design outcomes

Primary

MeasureTime frameDescription
Diagnostic valuethrough study completion, an average of 1 year]Sensitivity and Specificity of Al18F-octreotide PET/CT for SSTR positive tumors

Countries

China

Contacts

CONTACTGouzhu Hou, M.D.
15611145656@163.com15611145656
CONTACTXin Cheng, M.D.
cxpumc@foxmail.com15120002998
STUDY_DIRECTORRong Zheng, M.D.

National Cancer Center/Cancer Hospital, Chinese Academy of Medical Sciences and PUMC

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Apr 7, 2026