Actively Recruiting
Optimization of 18F-FDG PET/CT Imaging to Assess Treatment Response and Prognosis in High-Metabolism Lymphoma
Led by Ruijin Hospital · Updated on 2025-01-27
4000
Participants Needed
1
Research Sites
865 weeks
Total Duration
On this page
Sponsors
R
Ruijin Hospital
Lead Sponsor
Q
Qilu Hospital of Shandong University
Collaborating Sponsor
AI-Summary
What this Trial Is About
Researchers are working to develop a new way to evaluate how patients with high-metabolic lymphoma respond to treatment by using PET/CT imaging data. This method compares results from PET scans taken at the end of treatment with those taken partway through treatment, aiming to improve upon the existing Lugano classification criteria. The goal is to provide doctors with more accurate tools to assess treatment response and predict patient outcomes. The study uses a retrospective cohort design involving 4,000 patients with high-metabolic lymphoma who underwent 18F-FDG PET/CT scans before, during, and after treatment at multiple hospitals in China. Researchers manually outlined lymphoma lesions on the scans and used software to calculate key imaging parameters such as SUVmax, metabolic tumor volume, and total lesion glycolysis. Clinical data including age, gender, LDH levels, symptoms, lymphoma subtype, and treatment details were also collected. Participants' end-of-treatment PET/CT scans were evaluated both against baseline scans using the Lugano criteria and against interim scans to form a new response evaluation. The two methods were compared to identify any differences in treatment response assessments, and whether treatment plans changed based on the new evaluation. The study measures how well the new method predicts outcomes and aids in treatment decisions, with all assessments based on imaging and clinical data collected throughout the treatment period.
CONDITIONS
Official Title
Optimization of 18F-FDG PET/CT Response Assessment and Prognostic Evaluation Strategies for High-Metabolism Lymphoma
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Histopathologically confirmed high-metabolic lymphoma
- Underwent 18F-FDG PET/CT imaging before, during, and after treatment
- Treated with a standard first-line therapeutic regimen according to lymphoma treatment guidelines and individualized patient-specific considerations
- Complete clinicopathological and follow-up data available
You will not qualify if you...
- History of prior antitumor treatment
- History of other malignancies
- Incomplete clinical data or imaging records
- Presence of other concurrent malignant tumors
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Trial Site Locations
Total: 1 location
1
Ruijin Hospital affiliated to Shanghai Jiao Tong University of Medicine
Shanghai, Shanghai Municipality, China
Actively Recruiting
Research Team
R
Rui Guo
How is the study designed?
Study Type
OBSERVATIONAL
Masking
N/A
Allocation
N/A
Model
N/A
Primary Purpose
N/A
Number of Arms
2
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