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Updated: Apr 15, 2026

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Pretargeted Radioimmunotherapy Based on the Inverse Electron Demand Diels-Alder Reaction
Published on: January 29, 2019
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Radioimmunotherapy ((90) Y-Ibritumomab Tiuxetan) for Posttransplant Lymphoproliferative Disorders After Prior
J Rossignol1, L Terriou1, D Robu1
1Service des Maladies du Sang, CHRU de Lille, Lille, France.
Summary
Radioimmunotherapy (RIT) shows promise for treating relapsed/refractory CD20-positive posttransplantation lymphoproliferative disorders (PTLDs) when rituximab fails. This salvage therapy achieved complete responses in all patients who responded, with manageable toxicity.
Area of Science:
- Oncology
- Immunology
- Transplantation Medicine
Background:
- Posttransplantation lymphoproliferative disorders (PTLDs) are serious complications following transplantation.
- Rituximab monotherapy is effective in only half of CD20-positive PTLDs, with poor outcomes for relapsed/refractory cases.
- Some patients are ineligible for standard chemotherapy due to frailty or comorbidities.
Purpose of the Study:
- To evaluate the efficacy and safety of radioimmunotherapy (RIT) as a salvage treatment for rituximab-refractory/relapsed CD20-positive PTLDs.
- To assess RIT in patients ineligible for further chemotherapy.
Main Methods:
- Retrospective analysis of eight patients with rituximab-refractory/relapsed CD20-positive PTLDs.
- Treatment involved (90)Y-Ibritumomab tiuxetan (RIT) as a single agent (n=7) or combined with chemotherapy (n=1).
- Patients had undergone various solid organ transplants, including kidney, liver, and heart.
Main Results:
- An overall response rate of 62.5% was observed.
- All responders achieved a complete response (CR).
- At a median follow-up of 37 months, CR was ongoing in four patients; toxicity was primarily hematological and manageable. No graft rejection occurred.
Conclusions:
- Salvage RIT demonstrates potential efficacy for early rituximab-refractory PTLDs.
- RIT offers a viable treatment option for patients ineligible for chemotherapy.
- The treatment was well-tolerated with no unexpected toxicities, including graft rejection.
Keywords:
Cancerclinical researchcomplication: malignanthematologyimmune deficiencymalignancyneoplasia: chemotherapyoncologyorgan transplantation in generalposttransplant lymphoproliferative disorder (PTLD)practice
