RecruitingNCT07122674

18F-Pentixafor PET in Hematologic Malignancies

Prospective Clinical Study of 18F-Pentixafor PET Imaging in Hematologic Malignancies


Sponsor

First Affiliated Hospital of Zhejiang University

Enrollment

100 participants

Start Date

Jul 1, 2025

Study Type

OBSERVATIONAL

Conditions

Summary

The aim of this study is to evaluate the efficacy of 18F-Pentixafor PET imaging in the diagnosis, staging and response evaluation of hematological malignancies.


Eligibility

Min Age: 18 YearsMax Age: 80 Years

Inclusion Criteria5

  • Age of 18-80 years old, both sexes, with behavioral capacity;
  • patients with suspected or confirmed hematological malignancies;
  • 18F-FDG PET or other imaging examinations should be performed according to the treatment plan;
  • For suspected patients, biopsy or needle biopsy is expected to obtain pathological results;
  • Can provide informed consent, can understand and comply with the requirements of the study.

Exclusion Criteria5

  • pregnant and lactating women;
  • patients with fear or radiophobia, or with mental disorder or primary affective disorder;
  • received ionizing radiation outside the scope of this study for clinical medical or scientific research purposes within the past year, resulting in an annual radiation exposure dose exceeding 50 mSv;
  • received investigational drugs or devices of uncertain efficacy or safety within 1 month;
  • Any condition that the chairpersons of the study consider that any link related to the study may cause harm or have potential harm.

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Interventions

DRUG18F-Pentixafor

Patients with hematological malignancies receive 55 MBq/kg of 18F-Pentixafor intravenously followed by PET/CT or PET/MR after 60min of injection.


Locations(1)

The First Affiliated Hospital of Zhejiang University School of Medicine

Hangzhou, Zhejiang, China

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NCT07122674


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