Seminars in Radiation Oncology
Volume 17, Issue 3 , Pages 176-183, July 2007

Radioimmunotherapy as a Therapeutic Option for Non-Hodgkin’s Lymphoma

  • Roger M. Macklis, MD

      Affiliations

    • Roger Macklis has received honoraria for teaching and lecturing from Biogen-IDEC and Glaxo-Smith-Kline. Biogen-IDEC has also contributed financial support to the Cleveland Clinic for his investigator-initiated clinical trials in the area of radioimmunotherapy. He has no equity in any involved commercial concern.
    • Corresponding Author InformationAddress reprint requests to Roger M. Macklis, MD, Department of Radiation Oncology, The Cleveland Clinic Foundation, 9500 Euclid Avenue, Desk T28, Cleveland, OH 44195.

Cleveland Clinic Lerner College of Medicine and Department of Radiation Oncology, Cleveland Clinic Foundation, Cleveland, OH.

Radioimmunotherapy (RIT) represents a relatively new antibody-based radiopharmaceutical treatment for patients with various kinds of tumors. Although the field has a long history of preclinical and clinical investigations using many different agents, to date, only 2 of these immunologically targeted radiopharmaceuticals have been cleared for commercial sale. Both of these agents (90Y-ibritumomab tiuxetan or “Zevalin” [Biogen-Idec, Boston, MA] and 131I-tositumomab or “Bexxar” [GlaxoSmithKline Research, Triangle Park, NC]) are directed against the CD20 surface antigen found on normal mature B cells and greater than 95% of B-cell non-Hodgkin lymphoma (NHL). Both compounds produce similar impressive clinical outcomes (approximately 20%-40% complete response rates and 60%-80% overall response rates for patients with indolent B-cell NHL). Current protocol-based investigations of anti-CD20 RIT relate to new clinical uses and new CD20+ targets.

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PII: S1053-4296(07)00014-8

doi:10.1016/j.semradonc.2007.02.003

Seminars in Radiation Oncology
Volume 17, Issue 3 , Pages 176-183, July 2007