About this trial
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 criteria
Qualifiers
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;
Disqualifiers
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;
Trial design
Treatments tested in this trial
- 18F-Pentixafor