FDG-PET/CT imaging parameters for predicting spontaneous regression of methotrexate-associated lymphoproliferative disorder in patients with rheumatoid arthritis

Author:

Kameda Tomohiro,Nakashima Shusaku,Mitamura Katsuya,Yamamoto Yuka,Norikane Takashi,Shimada Hiromi,Wakiya Risa,Kato Mikiya,Miyagi Taichi,Sugihara Koichi,Mino Rina,Mizusaki Mao,Kadowaki Norimitsu,Dobashi Hiroaki

Abstract

AbstractIn this study, we investigated the usefulness of FDG-PET/CT for predicting spontaneous regression in methotrexate-associated lymphoproliferative disorder (MTX-LPD). Twenty patients with rheumatoid arthritis who were diagnosed with MTX-LPD were enrolled in the study. These patients were divided into those who showed spontaneous regression (SR group: ten patients) and those who received chemotherapy after discontinuation of MTX (CTx group: ten patients). Between-group differences in potential biomarkers were compared, including clinical markers at the onset of LPD [serum LDH and interleukin 2 receptor (sIL-2R)], change in absolute number of peripheral lymphocytes (ΔALC) over follow-up, and the FDG-PET/CT-derived parameters of maximum standardized uptake value (SUVmax), mean SUV (SUVmean), peak SUV (SUVpeak), sum of the metabolic tumor volume (MTVsum), and sum of total lesion glycolysis (TLGsum). The levels of sIL-2R, MTVsum, and TLGsum were significantly lower in the SR group than in the CTx group. In addition, ΔALC was higher in the SR group. In conclusion, MTV and TLG values measured by FDG-PET/CT may be suitable for use as predictors of SR in patients with MTX-LPD.

Publisher

Springer Science and Business Media LLC

Subject

Multidisciplinary

Reference22 articles.

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4. Harris, N. L. & Swerdlow, S. H. Methotrexate-associated lymphoproliferative disorders. In Pathology and Genetics of Tumours of Haematopoietic and Lymphoid Tissues Lyon (eds Jaffe, E. S. et al.) 270–271 (IARC Press, 2001).

5. Gaulard, P., Swerdlow, S.H., Harris, N.L., Sundstrdm, C., & Jaffe, E.S. Other iatrogenic immunodeficiency-associated lymphoproliferative disorders. in WHO Classification of Tumours of Haematopoietic and Lymphoid Tissues (Swerdlow, S.H., Campo, E., Harris, N.L. et al. eds). 4th edn. 462–444 (IARC, 2017).

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