About this trial
This multicenter study aims to evaluate the predictive value of tumor microenvironment PET/CT imaging for treatment response and prognosis in patients with aggressive lymphoma. Eligible patients with histologically confirmed aggressive lymphoma will undergo FAPI PET/CT imaging, and selected patients who are candidates for immunotherapy will undergo Grazytracer PET/CT imaging. These imaging methods are intended to assess fibroblast activation protein expression and granzyme B activity in lymphoma lesions, reflecting cancer-associated fibroblasts and cytotoxic T-cell activity in the tumor microenvironment. The study will explore optimal imaging assessment criteria and develop clinical-pathological-imaging models to predict treatment response, prognosis, and the relationship between tumor heterogeneity and refractory or relapsed disease.
Eligibility criteria
Qualifiers
Histologically confirmed aggressive lymphoma.
Baseline PET/CT showing moderate to high FDG uptake in lymphoma lesions.
No previous history of malignant tumors.
No significant cardiac, hepatic, or renal dysfunction.
Disqualifiers
Low FDG uptake on baseline PET/CT.
Lymphoma lesions have been surgically removed, with no positive lesions available for evaluation.
Active or uncontrolled chronic inflammation or infection.
Uncontrolled diabetes mellitus.
Trial design
Treatments tested in this trial
- Al18F-NOTA-FAPI
- Al18F-NOTA-grazytracer/68Ga-grazytracer