Currently, there are limited methods available in clinical practice to distinguish pseudoprogression after immunotherapy. Most patients rely on follow-up observations to monitor the disease, which does not meet clinical needs. 68Ga-grazytracer is a novel imaging agent targeting granzyme B. By detecting the concentration of granzyme B, it reflects the localization of cytotoxic T cells in the tumor region and their potential ability to kill tumor cells. This study aims to leverage the simplicity, non-invasiveness, visualization, and semi-quantitative advantages of 68Ga-grazytracer PET imaging to evaluate its effectiveness and feasibility in diagnosing pseudoprogression.
Study Type
OBSERVATIONAL
Enrollment
30
Ruijin Hospital, Shanghai Jiao Tong University School of Medicine
Shanghai, Shanghai Municipality, China
RECRUITINGDiagnostic performance 1
Sensitivity and specificity of 68Ga-grazytracer PET in diagnosing pseudoprogression
Time frame: Follow-up for 4-8 weeks, not exceeding 12 weeks.
Diagnostic performance 2
Investigating the optimal uptake value for 68Ga-grazytracer PET/CT imaging in diagnosing pseudoprogression.
Time frame: Follow-up for 4-8 weeks, not exceeding 12 weeks.
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