Seminars in Oncology
Volume 31, Issue 1 , Pages 68-82, February 2004

Targeted cancer therapy and immunosuppression using radiolabeled monoclonal antibodies

  • Wolfgang A Bethge

      Affiliations

    • Clinical Research Division, Fred Hutchinson Cancer Research Center, Seattle, WA, USA
  • ,
  • Brenda M Sandmaier

      Affiliations

    • Corresponding Author InformationAddress reprint requests to Brenda M. Sandmaier, MD, Fred Hutchinson Cancer Research Center, 1100 Fairview Ave N D1-100, Seattle, WA 98109-1024, USA
    • Department of Medicine, University of Washington, Seattle, WA, USA

Abstract 

Radioimmunotherapy (RIT) as a means to target radiation therapy to tumor cells or to specifically suppress host immunity specifically in the setting of allogeneic transplantation is a promising new strategy in the armory of today’s oncologist. Different approaches of RIT such as injection of a stable radioimmunoconjugate or the use of pretargeting are available. The choice of the radionuclide used for RIT depends on its radiation characteristics with respect to the malignancy or cells targeted. β-Emitters with their lower energy and longer path length are more suitable for targeting bulky, solid tumors, whereas α-emitters with their high linear energy transfer and short path length are better suited to target cells or tumors of the hematologic system. Encouraging results have been obtained using these approaches treating patients with hematologic malignancies. While the results in solid tumors are somewhat less favorable, new strategies for patients with minimal residual disease (MRD), using adjuvant and locoregional treatment, are currently being investigated. In this report, we outline basic principles of RIT, give an overview of available radioimmunoconjugates and their clinical applications with special emphasis on their use in hematologic malignancies, including use in conditioning regimens for stem cell transplantation (SCT).

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 Supported in part by Grants No. HL36444, CA78902, and CA15704 awarded by the National Institutes of Health, Department of Health and Human Services, Bethesda, MD, and by a grant from the Gabrielle Rich Leukemia Foundation. W.A.B. was supported by a fellowship from Deutsche Krebshilfe, Dr. Mildred-Scheel-Stiftung für Krebsforschung.

PII: S0093-7754(03)00566-9

doi:10.1053/j.seminoncol.2003.11.004

Seminars in Oncology
Volume 31, Issue 1 , Pages 68-82, February 2004