NK/T-cell Lymphoma Clinical Trial
Official title:
PET/MR in the Staging and Efficacy Evaluation of Newly Diagnosed NK/T-cell Lymphoma: a Prospective, Single-arm Clinical Study
NCT number | NCT05662540 |
Other study ID # | NK-PETMR |
Secondary ID | |
Status | Recruiting |
Phase | N/A |
First received | |
Last updated | |
Start date | May 26, 2023 |
Est. completion date | October 2026 |
Verified date | June 2023 |
Source | Ruijin Hospital |
Contact | Weili Zhao |
Phone | +862164370045 |
zwl_trial[@]163.com | |
Is FDA regulated | No |
Health authority | |
Study type | Interventional |
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.
Status | Recruiting |
Enrollment | 40 |
Est. completion date | October 2026 |
Est. primary completion date | October 2025 |
Accepts healthy volunteers | No |
Gender | All |
Age group | 14 Years to 70 Years |
Eligibility | Inclusion Criteria: - 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 - Patient has not been treated before for NK/T cell lymphoma - Commit to abide by the research procedures and cooperate with the implementation of the whole process of research - Written informed consent Exclusion Criteria: - Subjects who meet any of the following criteria are not eligible for study entry - Diagnosed aggressive NK cell leukemia - Pregnant or lactating women - Liver and kidney insufficiency - Other PET/MR contraindications: 1. Those with implanted functional electronic devices such as cardiac pacemakers 2. Carotid aneurysm clipping and other implants are ferromagnetic materials 3. Implanted perfusion devices such as insulin perfusion pumps 4. Those who do not cooperate in examinations such as coma, mental illness, and critically ill patients 5. Those who are claustrophobic - Other concurrent and uncontrolled medical conditions that the investigator believes will affect the patient's participation in the study |
Country | Name | City | State |
---|---|---|---|
China | Ruijin Hospital | Shanghai | Shanghai |
Lead Sponsor | Collaborator |
---|---|
Ruijin Hospital |
China,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | The sensitivity, specificity and accuracy of PET/MR in the staging of newly diagnosed NK/T-cell lymphoma patients | SUVmax, organs, et al. | Baseline | |
Primary | The sensitivity, specificity and accuracy of PET/MR in the efficacy evaluation of newly diagnosed NK/T-cell lymphoma patients | SUVmax, organs, et al. | After at least 2 cycles | |
Secondary | 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. | Baseline up to data cut-off (up to approximately 4 years) |
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