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

Eur J Nucl Med Mol Imaging. 2004 Apr;31(4):547-54. doi: 10.1007/s00259-003-1413-9. Epub 2004 Jan 14.

Abstract

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 micro g 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 (149)Tb is worthy of consideration as a new-generation radio-immunotherapeutic approach.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Alpha Particles / therapeutic use
  • Animals
  • Antibodies, Monoclonal / pharmacokinetics*
  • Antibodies, Monoclonal / therapeutic use*
  • Antibodies, Monoclonal, Murine-Derived
  • Antineoplastic Agents / therapeutic use
  • Apoptosis / radiation effects
  • Cell Line, Tumor
  • Cell Survival / radiation effects
  • Dose-Response Relationship, Drug
  • Drug Delivery Systems / methods
  • Evidence-Based Medicine / methods
  • Female
  • Leukemia / drug therapy
  • Leukemia / metabolism*
  • Leukemia / radiotherapy*
  • Mice
  • Mice, SCID
  • Organ Specificity
  • Radioimmunotherapy / methods*
  • Radiopharmaceuticals / therapeutic use
  • Reproducibility of Results
  • Rituximab
  • Survival
  • Tissue Distribution
  • Treatment Outcome

Substances

  • Antibodies, Monoclonal
  • Antibodies, Monoclonal, Murine-Derived
  • Antineoplastic Agents
  • Radiopharmaceuticals
  • terbium-rituximab
  • Rituximab