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Article type: Research Article
Authors: Tran, L.a; * | Huitema, A.D.R.a | van Rijswijk, M.H.b | Dinant, H.J.b | Baars, J.W.c | Beijnen, J.H.a; d | Vogel, W.V.e
Affiliations: [a] Department of Pharmacy & Pharmacology, The Netherlands Cancer Institute / Slotervaart Hospital, Amsterdam, The Netherlands | [b] Department of Rheumatology, Slotervaart Hospital, Amsterdam, The Netherlands | [c] Department of Medical Oncology, The Netherlands Cancer Institute / Antoni van Leeuwenhoek Hospital, Amsterdam, The Netherlands | [d] Faculty of Pharmaceutical Sciences, Department of Biomedical Analysis, Section of Drug Toxicology, Utrecht University, Utrecht, The Netherlands | [e] Department of Nuclear Medicine, The Netherlands Cancer Institute / Antoni van Leeuwenhoek Hospital, Amsterdam, The Netherlands
Correspondence: [*] Corresponding author: Ly Tran, PharmD, Slotervaart Hospital, Department of Pharmacy & Pharmacology, P.O. Box 90440, 1006 BK, Amsterdam, The Netherlands. Tel.: +31 20 512 4665; Fax: +31 20 512 4753; E-mail: Ly.Tran@slz.nl.
Abstract: Introduction:Visualization of the CD20-antigen expression could provide a tool to localize sites of inflammation and could be of additive value in the diagnosis, and subsequently, in the treatment follow-up of patients with rheumatoid arthritis. In this study, an anti-CD20 monoclonal antibody, rituximab (Mabthera®), was radiolabeled with 124Iodine. We report the first results of 124I-rituximab PET/CT in patients with rheumatoid arthritis. Methods:Eligible patients received 50 MBq 124I-rituximab. Wholebody PET/CT imaging was performed at 10 min, 24 h, 48 h and 72–96 h post injection. Images were evaluated primarily on a visual basis and were correlated with disease activity as determined by physical examination and clinical measures. Results:Joints with visually detectable targeting of 124I-rituximab were observed in 4 out of 5 evaluable patients. Only the images at 24 h and later showed accumulation in joints, indicating that the visualized signal represented active targeting of rituximab to the CD20 antigen. Several images showed CD20 positive B-cell infiltration in joints which were clinically normal, while a few clinically diagnosed arthritis localizations were not visualized. This discrepancy suggests that infiltration of CD20 positive B-cells in synovium is a phenomenon that is at least partially independent of clinical inflammation. The level of uptake in joints was generally low, representing less than 0.5% of the injected dose. Conclusion:We have shown the feasibility of CD20 antigen imaging using 124I-rituximab in patients with rheumatoid arthritis. Further research is needed to elucidate the clinical significance of demonstrated B-cell infiltration in rheumatic joints.
DOI: 10.3233/HAB-2011-0239
Journal: Human Antibodies, vol. 20, no. 1-2, pp. 29-35, 2011
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