Where does 90Y-ibritumomab tiuxetan radioimmunotherapy fit? Selecting the right patient


Published: June 17, 2009
Abstract Views: 192
PDF: 405
Publisher's note
All claims expressed in this article are solely those of the authors and do not necessarily represent those of their affiliated organizations, or those of the publisher, the editors and the reviewers. Any product that may be evaluated in this article or claim that may be made by its manufacturer is not guaranteed or endorsed by the publisher.

Authors

Radioimmunotherapy (RIT) with targeted monoclonal antibodies that emit ionising radiation is an effective treatment modality for B-cell non-Hodgkin’s lymphoma (NHL). RIT is designed to elicit anti-tumour effects through immunological and radiolytic mechanisms of action, and B-cell lymphomas are particularly ideal targets as they are inherently sensitive to radiation and express cell-surface antigens suitable for targeting. Yttrium-90 (90Y)-ibritumomab tiuxetan (Zevalin®), an anti-CD20 murine monoclonal antibody linked to the radionuclide 90Y, is the only form of RIT commercially available in Europe. 90Y-ibritumomab tiuxetan is licensed by the European Medicines Agency for therapy of adult patients with rituximab-relapsed or refractory CD20+ follicular B-cell NHL. Treatment with 90Y-ibritumomab tiuxetan comprises a short-course regimen that involves only a single dose of radioactive antibody. In a randomised phase III trial in rituximab-naïve patients with relapsed or refractory low-grade follicular or transformed CD20+ NHL, the overall response rate to 90Y-ibritumomab tiuxetan therapy was 80%, compared with 56% in patients treated with rituximab. 90Y-ibritumomab tiuxetan has also demonstrated efficacy in patients with multiple prior therapies and bulky tumours, along with elderly patients. The use of 90Y-ibritumomab tiuxetan is restricted to patients with <25% bone marrow infiltration by lymphoma cells, with reversible myelosuppression, manifesting clinically as cytopenias, as the dose-limiting toxicity. Because 90Y is a pure b-emitter with a short half-life, clinical therapy with 90Y-ibritumomab tiuxetan can be administered in an outpatient setting and patients released immediately afterwards unlike gamma radiation forms of RIT. Despite the nominal price of 90Y-ibritumomab tiuxetan, a single dose comprises an entire course of treatment and, as a third-line therapy, offers favourable cost-effectiveness when compared with that of rituximab.

Supporting Agencies


Bentz, M. (2009). Where does 90Y-ibritumomab tiuxetan radioimmunotherapy fit? Selecting the right patient. Hematology Meeting Reports (formerly Haematologica Reports), 1(5). https://doi.org/10.4081/hmr.v1i5.641

Downloads

Citations