Abstract
Ibritumomab tiuxetan labeled with yttrium-90 (90Y) is one of the excellent therapeutic options for patients with low-grade B cell non-Hodgkin lymphoma (NHL) who have relapsed disease after first-line chemotherapy regimens and are reluctant to the precedent therapy. The overall response rate (ORR) of 80–90% and the complete response rate (CR) of 30–69% have been reported for patients with relapsed or refractory low-grade B cell NHL. It has also an established role as a consolidation therapy agent after first-line chemotherapy. Ibritumomab tiuxetan has also proved to be an efficient and feasible treatment option as first-line therapy. The short-term toxicity associated with ibritumomab tiuxetan is mainly reversible bone marrow suppression. For diffuse large B cell lymphoma, which is the most frequent NHL subtype, ibritumomab tiuxetan has been also introduced as conditioning therapy added to conventional conditioning regimens before stem cell transplantation.
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- G-CSF:
-
Granulocyte colony-stimulating factor
- R-CHOP:
-
Rituximab, cyclophosphamide, doxorubicin hydrochloride, vincristine (oncovin), prednisolone
- R-CVP:
-
Cyclophosphamide, vincristine, prednisolone
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Choi, I., Uike, N. (2018). Clinical Use and Efficacy of Ibritumomab in B Cell Lymphoma. In: Hosono, M., Chatal, JF. (eds) Resistance to Ibritumomab in Lymphoma. Resistance to Targeted Anti-Cancer Therapeutics, vol 18. Springer, Cham. https://doi.org/10.1007/978-3-319-78238-6_1
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