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Randomized Controlled Trial of Yttrium-90–Labeled Ibritumomab Tiuxetan Radioimmunotherapy Versus Rituximab Immunotherapy for Patients With Relapsed or Refractory Low-Grade, Follicular, or Transformed B-Cell Non-Hodgkin’s Lymphoma

Witzig, Thomas E., Gordon, Leo I., Cabanillas, Fernando, Czuczman, Myron S., Emmanouilides, Christos, Joyce, Robin, Pohlman, Brad L., Bartlett, Nancy L., Wiseman, Gregory A., Padre, Norman, Grillo-López, Antonio J., Multani, Pratik, White, Christine A.·2002·Journal of Clinical Oncology

Abstract

PURPOSE: Radioimmunotherapy combines biologic and radiolytic mechanisms to target and destroy tumor cells, thus offering a needed therapeutic alternative for refractory non-Hodgkin’s lymphoma (NHL) patients. This phase III randomized study compares the novel radioimmunotherapy yttrium-90 (90 Y) ibritumomab tiuxetan with a control immunotherapy, rituximab, in 143 patients with relapsed or refractory low-grade, follicular, or transformed CD20+transformed NHL. PATIENTS AND METHODS: Patients received either a single intravenous (IV) dose of 90 Y ibritumomab tiuxetan 0.4 mCi/kg (n = 73) or rituximab 375 mg/m 2 IV weekly for four doses (n = 70). The radioimmunotherapy group was pretreated with two rituximab doses (250 mg/m 2) to improve biodistribution and one dose of indium-111 ibritumomab tiuxetan for imaging and dosimetry. The primary end point, overall response rate (ORR), was assessed by an independent, blinded, lymphoma expert panel. RESULTS: ORR was 80% for the 90 Y ibritumomab tiuxetan group versus 56% for the rituximab group (P = .002). Complete response (CR) rates were 30% and 16% in the 90 Y ibritumomab tiuxetan and rituximab groups, respectively (P = .04). An additional 4% achieved an unconfirmed CR in each group. Kaplan-Meier estimated median duration of response was 14.2 months in the 90 Y ibritumomab tiuxetan group versus 12.1 months in the control group (P = .6), and time to progression was 11.2 versus 10.1 months (P = .173) in all patients. Durable responses of ≥ 6 months were 64% versus 47% (P = .030). Reversible myelosuppression was the primary toxicity noted with 90 Y ibritumomab tiuxetan. CONCLUSION: Radioimmunotherapy with 90 Y ibritumomab tiuxetan is well tolerated and produces statistically and clinically significant higher ORR and CR compared with rituximab alone.

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Metadata

Authors
Witzig, T. E., Gordon, L. I., Cabanillas, F., Czuczman, M. S., Emmanouilides, C., Joyce, R., Pohlman, B. L., Bartlett, N. L., Wiseman, G. A., Padre, N., Grillo-López, A. J., Multani, P., & White, C. A.
Venue
Journal of Clinical Oncology
Published
2002-05-15
Volume
20
Issue
10
Pages
2453-2463
ISSN
  • 0732-183X (ISSN-L)
  • 1527-7755
OpenAlex
W2110646221
Cited by
1,170
References
3
FWCI
76.11
Type
journal article
Language
en
Open access
closed

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CoChat. (2026). Citation check: Randomized Controlled Trial of Yttrium-90–Labeled Ibritumomab Tiuxetan Radioimmunotherapy Versus Rituximab Immunotherapy for Patients With Relapsed or Refractory Low-Grade, Follicular, or Transformed B-Cell Non-Hodgkin’s Lymphoma. https://app.cochat.ai/papers/10.1200/jco.2002.11.076
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Witzig, T. E., Gordon, L. I., Cabanillas, F., Czuczman, M. S., Emmanouilides, C., Joyce, R., Pohlman, B. L., Bartlett, N. L., Wiseman, G. A., Padre, N., Grillo-López, A. J., Multani, P., & White, C. A. (2002). Randomized Controlled Trial of Yttrium-90–Labeled Ibritumomab Tiuxetan Radioimmunotherapy Versus Rituximab Immunotherapy for Patients With Relapsed or Refractory Low-Grade, Follicular, or Transformed B-Cell Non-Hodgkin’s Lymphoma. Journal of Clinical Oncology. https://doi.org/10.1200/jco.2002.11.076

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