Targeted alpha therapy in vivo:: direct evidence for single cancer cell kill using 149Tb-rituximab

被引:88
作者
Beyer, GJ
Miederer, M
Vranjes-duric, S
Comor, JJ
Künzi, G
Hartley, O
Senekowitsch-Schmidtke, R
Soloviev, D
Buchegger, F
机构
[1] Univ Hosp Geneva, Div Nucl Med, CH-1211 Geneva 14, Switzerland
[2] Mem Sloan Kettering Canc Ctr, Dept Mol Pharmacol & Chem, New York, NY 10021 USA
[3] Vinca Inst Nucl Sci, Lab Radioisotopes, Belgrade, Serbia
[4] Vinca Inst Nucl Sci, Phys Lab, Belgrade, Serbia
[5] Univ Med Ctr, Dept Med Biochem, Geneva, Switzerland
[6] Tech Univ Munich, Clin Nucl Med, D-8000 Munich, Germany
[7] CERN, Div PPE, CH-1211 Geneva, Switzerland
关键词
alpha particle-emitting radionuclides; terbium-149; radio-immunotherapy; rituximab; leukaemia;
D O I
10.1007/s00259-003-1413-9
中图分类号
R8 [特种医学]; R445 [影像诊断学];
学科分类号
1002 ; 100207 ; 1009 ;
摘要
This study demonstrates high-efficiency sterilisation of single cancer cells in a SCID mouse model of leukaemia using rituximab, a monoclonal antibody that targets CD20, labelled with terbium-149, an alpha-emitting radionuclide. Radio-immunotherapy with 5.5 MBq labelled antibody conjugate (1.11 GBq/mg) 2 days after an intravenous graft of 5.10(6) Daudi cells resulted in tumour-free survival for >120 days in 89% of treated animals. In contrast, all control mice (no treatment or treated with 5 or 300 mug unlabelled rituximab) developed lymphoma disease. At the end of the study period, 28.4%+/-4% of the long-lived daughter activity remained in the body, of which 91.1% was located in bone tissue and 6.3% in the liver. A relatively high daughter radioactivity concentration was found in the spleen (12%+/-2%/g), suggesting that the killed cancer cells are mainly eliminated through the spleen. This promising preliminary in vivo study suggests that targeted alpha therapy with Tb-149 is worthy of consideration as a new-generation radio-immunotherapeutic approach.
引用
收藏
页码:547 / 554
页数:8
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