Chemokine Receptor 4–Targeted 68Ga-Pentixafor PET/CT in Response Assessment of Waldenström Macroglobulinemia/Lymphoplasmacytic Lymphoma

2021 ◽  
Vol Publish Ahead of Print ◽  
Author(s):  
Qingqing Pan ◽  
Xinxin Cao ◽  
Yaping Luo ◽  
Jian Li ◽  
Fang Li
2021 ◽  
Vol 11 (1) ◽  
Author(s):  
Qingqing Pan ◽  
Xinxin Cao ◽  
Yaping Luo ◽  
Jian Li ◽  
Fang Li

Abstract Purpose 68Ga-pentixafor PET/CT was reported to have a high sensitivity in detecting tumor involvement of Waldenström macroglobulinemia/lymphoplasmacytic lymphoma (WM/LPL) in our previous study. We aimed to further investigate the semi-quantitative measurements of 68Ga-pentixafor PET/CT in response assessment in WM/LPL. Methods Fifteen patients with WM/LPL were recruited in a prospective cohort study and underwent both 68Ga-pentixafor and 18F-FDG PET/CT at baseline and post-treatment. PET/CT-based responses were analyzed with semi-quantitative assessments of metabolic tumor volume (MTV) and total lesions glycolysis/uptake (TLGFDG and TLUCXCR4), and the correlation between PET/CT-based response and clinical response, monoclonal protein and IgM response was analyzed. Results After chemotherapy, 5 patients had complete response or very good partial response, 8 had partial response or minimal response and 2 had progressive disease. In quantitative analysis, 68Ga-pentixafor PET/CT-based response (measured in ∆TLUCXCR4%, ∆MTVCXCR4%, ∆SUVpeak%) showed a significant direct correlation with clinical response, monoclonal protein and IgM response (p < 0.01). However, 18F-FDG PET/CT-based response was independent from clinical response (p > 0.05). Conclusions The semi-quantitative measurements of 68Ga-pentixafor PET/CT outperformed 18F-FDG PET/CT in response assessment of WM/LPL.


2010 ◽  
Vol 102 (8) ◽  
pp. 557-567 ◽  
Author(s):  
S. Y. Kristinsson ◽  
J. Koshiol ◽  
M. Bjorkholm ◽  
L. R. Goldin ◽  
M. L. McMaster ◽  
...  

Hematology ◽  
2018 ◽  
pp. 1419-1431.e5
Author(s):  
Steven P. Treon ◽  
Jorge J. Castillo ◽  
Zachary R. Hunter ◽  
Giampaolo Merlini

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