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Chemokine Receptor 4 PET/CT Imaging of CXCR4-Related Diseases

Chemokine Receptor 4 PET/CT Imaging of CXCR4-Related Diseases

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT06690736
Enrollment
200
Registered
2024-11-15
Start date
2022-03-01
Completion date
2027-10-01
Last updated
2026-09-08

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

Conditions

CXCR4-related Disease, Metastasis, Positron Emission Tomography, Tumor

Keywords

PET/CT, Chemokine receptor 4, Pentixafor, Pentixather

Brief summary

To evaluate the potential usefulness of 68Ga/18F-Pentixafor/Pentixather positron emission tomography/computed tomography (PET/CT) for the diagnosis of primary and metastatic lesions in various CXCR4-related disease patients.

Detailed description

Subjects with various CXCR4-related disease patients underwent 68Ga/18F-Pentixafor/Pentixather PET/CT either for an initial assessment or for recurrence detection. Lesions uptake was quantified by the maximum standard uptake value (SUVmax). The sensitivity, specificity, positive predictive value (PPV), negative predictive value (NPV) and accuracy of 68Ga/18F-Pentixafor/Pentixather PET/CT were calculated.

Interventions

DIAGNOSTIC_TESTCXCR4 PET/CT Imaging

Each subject receive a single intravenous injection of 68Ga/18F-Pentixafor/Pentixather, and undergo PET/CT imaging within the specificed time.

Sponsors

Tianjin Medical University
Lead SponsorOTHER
Tianjin Medical University General Hospital
CollaboratorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
DIAGNOSTIC
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to 80 Years
Healthy volunteers
Yes

Inclusion criteria

* suspected or confirmed untreated Lymphoproliferative and other CXCR4-related diseases patients * 18F-FDG PET/CT within two weeks * signed written consent.

Exclusion criteria

* pregnancy * breastfeeding * known allergy against Pentixafor

Design outcomes

Primary

MeasureTime frameDescription
Standardized uptake value (SUV)30 daysStandardized uptake value (SUV) of FAPI for each target lesion of subject or suspected primary tumor or/and metastasis.

Secondary

MeasureTime frameDescription
Diagnostic efficacy30 daysThe sensitivity, specificity and accuracy of FAPI PET/CT were calculated.

Countries

China

Contacts

CONTACTHaonan Yu, MD
dreamadam@126.com+8613821000597
CONTACTShaobo Yao, PhD
yaoshaobo008@163.com+8615122570279

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Sep 9, 2026