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Tumor PET imaging technology targeting chemokine receptor 4

Tumor PET imaging technology targeting chemokine receptor 4

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2600121072
Enrollment
Unknown
Registered
2026-03-25
Start date
2026-04-01
Completion date
Unknown
Last updated
2026-03-30

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

Conditions

Tumors with High CXCR4 Expression

Interventions

Gold Standard:Pathological tissue CXCR4 expression level

Sponsors

The First Affiliated Hospital of Chongqing Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 75 Years

Inclusion criteria

Inclusion criteria: (1) Aged 18 to 75 years (inclusive), regardless of gender; (2) Clinically suspected or diagnosed with one of the following diseases, and planned or in need of whole-body evaluation of CXCR4 receptor status: 1) Department of Endocrinology/Urology: Patients clinically suspected of having primary hyperaldosteronism requiring diagnosis and subtyping (e.g., differentiation between adrenal adenoma and hyperplasia); or patients with Cushing's syndrome suspected of having cortisol-secreting adenoma, who should have completed surgical treatment. 2) Department of Hematology: Patients with newly diagnosed or relapsed/refractory hematologic malignancies such as multiple myeloma or lymphoma (e.g., mantle cell lymphoma, marginal zone lymphoma, etc.). 3) Department of Neurosurgery: Patients with suspected or diagnosed pituitary tumors. (3) The patient is informed and voluntarily signs a written informed consent form.

Exclusion criteria

Exclusion criteria: 1.Pregnant or nursing women 2.A known history of severe allergies to [68Ga]Ga-Pentixafor or its analogues 3.Received chemotherapy, targeted therapy, radiotherapy, immunotherapy or participated in other radiopharmaceutical intervention clinical studies within 4 weeks before the first imaging 4.Suffering from any serious disease that is difficult to control (such as active severe infection, New York Heart Function Class III-IV heart failure, severe liver and kidney dysfunction, etc.) 5.Any circumstances that are inappropriate for PET/CT examination (such as claustrophobia, inability to lie flat for more than 30 minutes, etc.) 6.The investigator judges that there are other circumstances that are inappropriate to participate in this study

Design outcomes

Primary

MeasureTime frame
SUVmax;

Secondary

MeasureTime frame
SUVmean;Metabolic Tumor Volume;

Countries

China

Contacts

Public ContactHua Pang

The First Affiliated Hospital of Chongqing Medical University

Zuor1997@163.com+86 89011714

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Apr 4, 2026