4.0 Article

Radioimmunotherapy for B-cell non-Hodgkin lymphoma

Journal

BEST PRACTICE & RESEARCH CLINICAL HAEMATOLOGY
Volume 19, Issue 4, Pages 655-668

Publisher

ELSEVIER SCI LTD
DOI: 10.1016/j.beha.2006.05.002

Keywords

radioimmunotherapy; NHL; ibritumomab tiuxetan (Zevalin (TM)); tositumomab (Bexxar (TM)); CD20; radioimmunoconjugate

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Funding

  1. NCI NIH HHS [CA97274] Funding Source: Medline
  2. NATIONAL CANCER INSTITUTE [P50CA097274] Funding Source: NIH RePORTER

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Radioimmunotherapy (RIT) combines the targeting advantage of a monoclonal antibody with the radiosensitivity of non-Hodgkin lymphoma (NHL) cells. There are now two radioimmunoconjugates (RICs) - ibritumomab tiuxetan (Zevalin(TM)) and tositumomab (Bexxar(TM)) - that are approved by the FDA in the US for relapsed low-grade or follicular B-cell NHL. Both agents target the CD20 antigen on B-cell lymphoma cells. In relapsed disease, single doses of RIT produce an 80% overall response rate, with approximately 20% of patients achieving durable responses. RIT is very well tolerated and is delivered on an outpatient basis over I week. The only significant toxicity is reversible myelosuppression. Both RIT agents have demonstrated high anti-tumor activity in patients who are refractory to rituximab. Current trials are testing RIT as initial therapy with rituximab maintenance, as adjuvant therapy after chemotherapy, or in high-dose protocols with stem-cell support.

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