Why the study?
To evaluate CXCR4 expression using [68Ga]pentixafor PET/CT across a spectrum of non-Hodgkin lymphomas and compare it with [18F]FDG PET/CT.
Does [68Ga]pentixafor PET/CT improve the detection of disease involvement in non-Hodgkin lymphoma compared to [18F]FDG PET/CT?
Does [68Ga]pentixafor PET/CT improve the detection of disease involvement in non-Hodgkin lymphoma compared to [18F]FDG PET/CT?
[68Ga]pentixafor PET/CT shows higher uptake than [18F]FDG in lymphoplasmacytic and marginal zone lymphomas, suggesting its potential utility for staging these specific subtypes.
May support [68Ga]pentixafor PET for staging lymphoplasmacytic and marginal zone lymphoma; hypothesis-generating and leaves open prospective validation versus [18F]FDG.
Background In order to study the CXCR4 expression with [ 68 Ga]pentixafor PET in different types of non-Hodgkin lymphoma, we performed a retrospective study to describe the [ 68 Ga]pentixafor PET/CT imaging in a spectrum of lymphomas and to compare it with [ 18 F]FDG PET/CT. Results Twenty-seven patients with newly diagnosed non-Hodgkin lymphoma were recruited retrospectively. [ 68 Ga]pentixafor PET showed increased radioactivity in lymphoplasmacytic lymphoma ( n = 8), marginal zone lymphoma ( n = 4), diffuse large B cell lymphoma ( n = 3), follicular lymphoma ( n = 2), mantle cell lymphoma ( n = 1), unclassified indolent B cell lymphoma ( n = 3), and enteropathy associated T cell lymphoma ( n = 3). However, peripheral T cell lymphoma, not otherwise specified ( n = 1), and NK/T cell lymphoma ( n = 2) were not avid for [ 68 Ga]pentixafor. In comparison to [ 18 F]FDG PET, [ 68 Ga]pentixafor PET demonstrated more extensive disease and higher radioactivity in lymphoplasmacytic lymphoma and marginal zone lymphoma. Conclusion CXCR4 expression varies in different types of non-Hodgkin lymphoma. Overexpression of CXCR4 was detected with [ 68 Ga]pentixafor PET/CT in lymphoplasmacytic lymphoma, marginal zone lymphoma, diffuse large B cell lymphoma, follicular lymphoma, mantle cell lymphoma, unclassified indolent B cell lymphoma, and enteropathy associated T cell lymphoma. The uptake of [ 68 Ga]pentixafor was higher than [ 18 F]FDG in lymphoplasmacytic lymphoma and marginal zone lymphoma.
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Pan et al. (2020) studied this question.
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