About this trial
This study intends to evaluate the application value of Positron Emission Tomography/Magnetic Resonance (PET/MR) in the staging and efficacy evaluation of NK/T cell lymphoma, aiming to explore a more accurate system for predicting the prognosis of patients and guiding the treatment.
Eligibility criteria
This trial does not accept healthy volunteersQualifiers
Pathologically diagnosed NK/T-cell lymphoma based on the WHO classification 2016
Age from 14 to 70 years-old
ECOG 0-2 score
Patients with a life expectancy of at least 6 months
Disqualifiers
Diagnosed aggressive NK cell leukemia
Pregnant or lactating women
Liver and kidney insufficiency
Those with implanted functional electronic devices such as cardiac pacemakers
Trial design
Single group
Treatments tested in this trial
Positron Emission Tomography/Magnetic Resonance (PET/MR)
Device18F-FDG PET/MR imaging (manufacturer: Siemens, model: Biography mMR). Research devices are marketed products.
Treatment groups
Trial outcomes
Primary outcomes
The sensitivity, specificity and accuracy of PET/MR in the staging of newly diagnosed NK/T-cell lymphoma patients
SUVmax, organs, et al.
The sensitivity, specificity and accuracy of PET/MR in the efficacy evaluation of newly diagnosed NK/T-cell lymphoma patients
SUVmax, organs, et al.
Secondary outcomes
Exploratory construction of prognostic prediction or efficacy evaluation system for newly treated NK/T-cell lymphoma based on PET/MR imaging indicators.
SUVmax, organs, progression-free survival, overall survival, et al.
Sponsors and contacts
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